Technical

Publications
Direction 2273022-100
Revision 19

Proteus XR/a System

(32, 50, 65, 80kW)

Service Manual

Copyright © 2000, 2001, 2002, 2003, 2004, 2005, 2006 by General Electric Co.

Service Documentation
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

ii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Direction 2273022-100
Revision 19

Proteus XR/a System

Service Manual

IMPORTANT! . . . X-RAY PROTECTION

X-Ray equipment if not properly the operator to take adequate The equipment is sold with the
used may cause injury. precautions to prevent the understanding that the General
Accordingly, the instructions possibility of any persons Electric Company, Medical
herein contained should be carelessly exposing themselves or Systems Group, its agents, and
thoroughly read and others to radiation. representatives have no
understood by everyone who responsibility for injury or damage
will use the equipment before It is important that everyone which may result from improper
you attempt to place this having anything to do with x- use of the equipment.
equipment in operation. The radiation be properly trained and
General Electric Medical fully acquainted with the Various protective material and
Systems Group, will be glad to recommendations of the National devices are available. It is urged
assist and cooperate in placing Council on Radiation Protection that such materials or devices be
this equipment in use. and Measurements as published used.
in NCRP Reports available from
Although this apparatus NCRP Publications, 7910 CAUTION: United States
incorporates a high degree of Woodmont Avenue, Room 1016, Federal law restricts this
protection against x-radiation Bethesda, Maryland 20814, and
of the International Commission device to use by or on the
other than the useful beam, no
practical design of equipment can on Radiation Protection, and take order of a physician.
provide complete protection. Nor adequate steps to protect against
can any practical design compel injury.

i
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

If you have any comments, suggestions or corrections to the information in this document,
please write them down, include the document title and document number, and send them to:

GENERAL ELECTRIC MEDICAL SYSTEMS

MANAGER – INFORMATION INTEGRATION,
AMERICAS W–622
P.O. BOX 414
MILWAUKEE, WI 53201–0414

ii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

REGULATORY REQUIREMENTS

This product conforms with the requirements of Council Directive 93/42/EEC concerning medical devices
when it bears the following CE marking of conformity:

0459

iii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Electromagnetic Compatibility (EMC)

This product conforms with IEC60601-1-2:2001 EMC standard for medical devices.
Note: This equipment generates, uses, and can radiate radio frequency energy. The equipment
may cause or subject to radio frequency interference with other medical and non–medical
devices and radio communications. To provide reasonable protection against such
interference, the Proteus XR/a System (32, 50, 65, 80kW) complies with emissions limits for
a Group 1, Class A Medical Devices and has applicable immunity level as stated in EN
60601-1-2:2001.
However, there is no guarantee that interference will not occur in a particular installation.
Special precautions and other information regarding EMC provided in the accompanying
documents of this equipment shall be observed during installation and operation of this
equipment.

Note: If this equipment is found to cause interference (which may be determined by switching the
equipment on and off), the user (or qualified service personnel) should attempt to correct the
problem by one or more of the following measure(s):

• Reorient or relocate the affected device(s).

• Increase the separating space between the equipment and the affected device.
• Power the equipment from a source different from that of the affected device.
• Consult the point of purchase or service representative for further suggestions.
Use of accessories, transducers, cables and other parts other than those specified by the
WARNING manufacturer of this equipment may result in increased emissions or decreased immunity of
the equipment. The manufacturer is not responsible for any interference caused either by the
use of interconnect cables other than those recommended, or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could void the user’s
authority to operate the equipment.

Note: To comply with the regulations applicable to an electromagnetic interface for a Group 1,
Class A Medical Device, and to minimize interference risks, the following requirements shall
apply:

• All interconnect cables to peripheral devices must be shielded and properly

grounded. Use of cables not properly shielded and grounded may result in the
equipment causing radio frequency interference in violation of the European Union
Medical Device directive and FCC regulations.

• All of those recommended guidance regarding electromagnetic environment shall be

followed.

Note: Do not use devices which intentionally transmit RF signals (Cellular Phones, Transceivers, or Radio
Controlled Products) in the vicinity of this equipment as it may cause performance outside the
published specifications. Keep the power to these type devices turned off when near the equipment.
The medical staff in charge of this equipment is required to instruct technicians, patients, and
others.

iv
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Guidance and manufacturer’s declaration – Electromagnetic Emissions

The Proteus XR/a system is suitable for use in the specified electromagnetic environment. The
purchaser or user of the Proteus XR/a system should assure that it is used in an elec-
tromagnetic environment as described below:
Emissions Test Compliance Electromagnetic Environment
The Proteus XR/a system uses RF energy only for
RF Emissions Group1 its internal function. Therefore, its RF emissions are
CISPR11 very low and are not likely to cause any interference
in nearby electronic equipment.

RF Emissions Class A The Proteus XR/a system is suitable for use in all
CISPR11 establishments other than domestic and those
Harmonic emissions Not directly connected to the public low-voltage power
IEC 61000-3-2 applicable supply network that supplies buildings used for
Voltage fluctuations/ Not domestic
flicker emissions applicable purposes.
IEC 61000-3-3

v
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Guidance and manufacturer’s declaration - Electromagnetic Immunity (1)

The Proteus XR/a system is suitable for use in the specified electromagnetic environment. The
purchaser or user of the Proteus XR/a system should assure that it is used in an electromagnetic
environment as described below:
Immunity Test IEC 60601-1-2 Compliance Electromagnetic Environment
Test Level Level
Electrostatic ±6 kV contact ±6 kV contact Floors are wood, concrete, or ceramic
discharge (ESD) ±8 kV air ±8 kV air tile, or floors are covered with synthetic
IEC 61000-4-2 material and the relative humidity is at
least 30 %.
±2 kV for power ±2 kV for
Electrical fast supply lines power supply
transient/burst lines Mains power quality is that of a typical
IEC 61000-4-4 ±1 kV for commercial and/or hospital environment
input/output ±1 kV for
lines input/output
lines
±1 kV differential ±1 kV
Surge mode differential Mains power quality is that of a typical
IEC 61000-4-5 ±2 kV common mode commercial and/or hospital environment.
mode ±2 kV common
mode
Voltage dips, Mains power quality is that of a typical
short < 5 % UT 0 % UT for 5 commercial and/or hospital environment.
interruptions (> 95 % dip in UT) sec If the user of the Proteus XR/a system
and voltage for 0.5 cycle requires continued operation during
variations on power mains interruptions, it is
power supply 40 % UT recommended that the Proteus XR/a
input lines (60 % dip in UT) system be powered from an
IEC 61000-4-11 for 5 cycles uninterruptible power supply or a battery.

70 % UT
(30 % dip in UT)

< 5 % UT
(> 95 % dip in UT)
for 5 s
Power Power frequency magnetic fields are at
frequency 3 A/m 3 A/m levels characteristic of a typical location
(50/60 Hz) in a typical commercial and/or hospital
magnetic field environment.
IEC 61000-4-8

Note: These are guidelines. Actual conditions may vary.

vi
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Guidance and manufacturer’s declaration - Electromagnetic Immunity (2)

The Proteus XR/a system is suitable for use in the specified electromagnetic environment. The
purchaser or user of the Proteus XR/a system should assure that it is used in an electromagnetic
environment as described below:
Immunity IEC 60601-1-2 Compliance Electromagnetic Environment
Test Test Level Level
Portable and mobile RF communications
equipment are used no closer to any part of the
[EQUIPMENT and/or SYSTEM], including cables,
than the recommended separation distance
calculated from the equation appropriate for the
frequency of the transmitter.

Recommended separation distance

Conducted RF 3V
IEC 61000-4-6 150 kHz to [V1 =] 3 V d= 1.2
80 MHz
d= 1.2 80 MHz to 800 MHz
d= 2.3 800 MHz to 2,5 GHz

Note: P is the power rating of the transmitter in

Radiated RF 3 V/m
watts (W) according to the transmitter manufac-
IEC 61000-4-3 80 kHz to [E1=] 3 V/m
turer and d is the recommended separation dis-
800 MHz
tance in meters (m).

Field strengths from fixed RF transmitters, as

determined by an electromagnetic site survey,*
are less than the compliance level in each fre-
quency range.**

Interference may occur in the vicinity of equip-

ment marked with the following symbol:

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.

*Field strengths from fixed transmitters, such as base stations for cellular telephones and land mobile radios,
amateur radio, AM and FM radio broadcast, and TV broadcast cannot be estimated accurately. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be performed. If
the measured field strength exceeds the RF compliance level above, observe the Proteus XR/a system to
verify normal operation in each use location. If abnormal performance is observed, additional measures may be
necessary, such as re-orienting or relocating the [EQUIPMENT and/or SYSTEM].
**Over the frequency range 150 kHz to 80 MHz, field strengths are less than 3 V/m.
The Recommended Separation Distances are listed in the next table.
Note: These are guidelines. Actual conditions may vary.

vii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Recommended Separation Distances for Portable and Mobile RF Communications Equipment and the
Proteus XR/a system

Frequency of
Transmitter
150KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz

Equation
d= 1.2 d= 1.2 d= 2.3

Rated Power of
Transmitter DISTANCE DISTANCE DISTANCE
(W) (meters) (meters) (meters)
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23

For transmitters rated at a power not listed above, the DISTANCE can be estimated using the
equation in the corresponding column, where P is the power rating of the transmitter in watts (W)
according to the transmitter manufacturer.

Note: These are guidelines. Actual conditions may vary.

viii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

KUNDENDIENST – HANDBUCH ZU RATE GEZOGEN UND VERSTANDEN

WURDE.

ix
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

x
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

REVISION HISTORY
REVISION DATE OF ISSUE REASON FOR CHANGE
0 8, 24, 2000 FIRST RELEASE
1 9, 25, 2000 • Add table lubricant boxes replacement procedure.
• Add new table control board schematics and table control board adjusting
procedure.
• Update System Schematics and Tomo-link Schematics.
• Supplement tomo (option) installation procedure.
• Add collimator bulb replacement procedure.
• Modify touch screen calibration procedure.
• Update FRU parts list.
2 11,10,2000 • Update page i, 4-6, 4-7, 10-12 and 10-14
3 11,20,2000 • Add collimator mounting screws’ torque requirement. Chapter 2.
• Update renewal parts list and illustration. Chapter 9.
• Add collimator bulb replacement notes. Chapter 3.
• Update Schematics page numbers. Chapter 10.
• Add a note on removing vinyl protective films. Chapter 2.
• Add a note on ESC key in Service Software. Chapter 3.
• Add a trolley stud picture. Chapter 2.
• Add a torque requirement to Trunion screws. Chapter 2.
• Add a Trunion installation warning. Chapter 2.
4 02,05,2001 • Update renewal parts list. Chapter 9
• Update system console mounting Job Card. Chapter 2.
• Add printer mounting Job Card. Chapter 2.
• Add system console replacement Job Card. Chapter 3.
• Add notes. Chapter 2, 3, 4, 8.
• Add OTS console schematics. Chapter 10.
• Add DOSE Calibration Job Card. Chapter 4.
• Add collimator alignment Job Card. Chapter 4.
• Add printer cables connection. Chapter 2.
• Add collimator update Job Card. Chapter 3.
• Add a maintenance item about ‘LAT bar’. Chapter 8.
5 09,28,2001 • Update room dimension in Chapter 2
• Add collimator D1&D2 trouble shooting and replacement in Chapter 3
• Transfer the Job Card SW JEDI 7-4,7-3,7-2 from Chapter 3 to Chapter 4
• Update touch screen calibration and AEC calibration in Chapter4
• Add new error code in chapter 7
• Add new Job Card PM010 in Chapter 8
• Update renewal parts list in Chapter 9
• Add schematics in Chapter 10
6 11,16,2001 • Update collimator mounting procedure in Chapter 2
• Update PM010 in Chapter 8
7 06,21,2002 • Update renewal parts in Chapter 9
• Update 90WS SW installation in Chapter 4,Grip adjust/EMC in Chapter2
8 11,03,2002 • Update renewal parts in Chapter 9

xi
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

• Update Job Card for Table motor replacement in Chapter 3

9 07,25,2003 • Update renewal parts in Chapter 9
• Add Job Card IST 008, 012, 014, 016 for SG100 Wall Stand and MX100
X-ray tube assembling in Chapter 2
• Add Job Card IST 033 for Spanish language labels in Chapter 2
• Update Job Card CAL 002, 006, 007, 008, 010, SW JEDI 7-4,7-2, IST
JEDI 5-2 in Chapter 4
• Add Functional Check contents for SG100 Wall Stand in Chapter 5
• Add Collimator error codes in Chapter 7
• Add Planned Maintenance contents for SG100 Wall Stand in Chapter 8
• Update schematics in Chapter 10
10 07,28,2003 • Recover the contents for RAD21 tube
11 09,15,2003 • Change the database file name for MX100 tube
12 04,09,2004 • Update renewal parts in Chapter 9
• Update Job Card IST 16 in Chapter 2
• Update Job Card CAL 2 in Chapter 4
13 10, 29, 2004 • Update regulatory requirements
• Add Job Card IST 009, 016, 017 for SG120 Wall Stand and Eclipse
Proteus Collimator in Chapter 2
• Update IST 020, 021, 022, 023, 025, 033 for SG120 Wall Stand and
Eclipse Proteus Collimator in Chapter 2
• Update Job Card 006, 008, SW JEDI 7-2 in Chapter 4
• Add SG120 Wall Stand in Chapter 5
• Add Eclipse Proteus Collimator error codes in Chapter 7
• Add SG120 Wall Stand Planned Maintenance in Chapter 8
• Update renewal parts in Chapter 9
• Add SG120 Wall Stand Schematics in Chapter 10
14 07, 25, 2005 • Update Proteus System Console Software to V2.14
• Update IST 002 in Chapter 2
• Add notes in Chapter 2
• Add Caution in Chapter 3
• Update CAL 002 in Chapter 4
• Update Eclipse Proteus Collimator Error Codes in Chapter 7
• Update PM 004 in Chapter 8
• Update renewal parts in Chapter 9
• Update Table Schematic 221-3000 in Chapter 10
15 12.12,2005 • Add requirements of warning label in Chapter 2
• Add rotation limit screw in Chapter 2
• Delete a picture and add a section in section 5-3-3
• Change a warning and a picture of cable connection, add a note in
Chapter 2
• Add the content in Chapter 2
• Add 2 notes in Chapter 2
• Add a Job Card in Chapter 4
• Add a note and a tool in Chapter 8
• Change part No. in Chapter 9

xii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

• Change 2 picture in Chapter 9

16 02.15,2006 • Add description of GEHL Reciprocating Bucky and AID Ion Chamber in
Chapter 2 and Chapter 9
17 06.20, 2006 • Update warning label to meet HHS requirements in Chapter 2.
18 10.10, 2006 • Add LOTO contents in Chapter 1
• Add Notes and Warnings in IST 011 in Chapter 2
• Update Warning and add bucky jumpers pictures in IST 009 in Chapter 2
• Update motor replacement in Chapter 3
• Add Warning in system console replacement in Chapter 3
• Add Warning in Chapter 5
• Add bearing and shaft check procedures In PM004 in Chapter 8
• Update PDU Schematics in Chapter 10
19 12.15,2006 • Add Note in IST 015 in Chapter 2
• Update IST 016 in Chapter 2
• Update IST 017 in Chapter 2
• Add Note in Replace whole collimator in Chapter 3
• Update Replace collimator lamp assembly in Chapter 3
• Update Eclipse Proteus Collimator error codes in Chapter 7
• Update GPCP NO. and Description of OTS in Chapter 9
The version of this manual is shown at the upper left corner of this page.

xiii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

LIST OF EFFECTIVE PAGES

PAGE REVISION PAGE REVISION
NUMBER NUMBER NUMBER NUMBER
i Revision 1 4-38 Revision 7
1-1 thru 1-3 Revision 1 5-11 and 5-14 Revision 7
2-1 thru 2-27 Revision 1 8-2 and 8-19 Revision 7
3-1 thru 3-14 Revision 1 9-2 and 9-10 Revision 7
4-1 thru 4-5 Revision 1 9-4 thru 9-7 Revision 7
4-8 thru 4-58 Revision 1 9-19 and 9-22 Revision 7
5-1 thru 5-21 Revision 1 3-11 thru 3-16 Revision 8
6-1 thru 6-9 Revision 1 3-24 Revision 8
7-1 thru 7-43 Revision 1 9-4 Revision 8
8-1 thru 8-20 Revision 1 1-3 Revision 9
8-1 thru 8-20 Revision 1 2-1 thru 2-2 Revision 9
9-1 thru 9-78 Revision 1 2-4 thru 2-5 Revision 9
10-1 thru 10-11, 13 Revision 1 2-20 thru 2-27 Revision 9
10-15 thru 10-37 Revision 1 2-35 thru 2-59 Revision 9
4-6 thru 4-7 Revision 2 2-60 thru 2-61 Revision 9
ii thru xii Revision 2 2-63 Revision 9
10-12 and 10-14 Revision 2 2-66 Revision 9
2-11 Revision 3 2-68 Revision 9
2-21 and 2-22 Revision 3 2-74 thru 2-75 Revision 9
2-42 Revision 3 2-78 thru 2-79 Revision 9
3-38 Revision 3 3-35 thru 3-37 Revision 9
9-1 thru 9-18 Revision 3 4-1 Revision 9
10-12 and 10-14 Revision 3 4-4 thru 4-6 Revision 9
2-18 thru 2-24 Revision 4 4-12 thru 4-22 Revision 9
9-12 thru 9-18 Revision 4 4-25 Revision 9
3-41 Revision 4 4-27 Revision 9
4-11 thru 4-13 Revision 4 4-35 thru 4-36 Revision 9
8-1 thru 8-2 Revision 4 4-44 Revision 9
10-38 thru 10-42 Revision 4 4-84 thru 4-87 Revision 9
4-58 thru 4-60 Revision 4 5-5 thru 5-11 Revision 9
2-43 Revision 4 7-13 Revision 9
3-42 Revision 4 7-29 Revision 9
3-33 Revision 4 8-2 Revision 9
1-3 Revision 5 8-20 thru 8-22 Revision 9
2-12 and 2-28 Revision 5 9-1 thru 9-9 Revision 9
3-6 thru 3-10 Revision 5 9-14 thru 9-15 Revision 9
4-5 Revision 5 9-18 Revision 9
4-15 Revision 5 9-22 thru 9-25 Revision 9
4-17 thru 4-36 Revision 5 9-27 Revision 9
4-57 thru 4-58 Revision 5 9-33 Revision 9
5-4 Revision 5 9-45 thru 9-48 Revision 9
7-10 thru 7-27 Revision 5 10-1 thru 10-3 Revision 9
8-20 Revision 5 10-5 thru 10-12 Revision 9
9-5 Revision 5 10-13 Revision 9
10-24 Revision 5 10-17 Revision 9
2-27 thru 2-28 Revision 6 2-36 Revision 10
8-20 Revision 6 2-39 Revision 10
2-39 and 2-40 Revision 7 2-41 Revision 10
2-48 Revision 7 2-45 thru 2-50 Revision 10
4-4 and 4-5 Revision 7 2-63 Revision 10

xiv
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

4-25 Revision 10 2-57 Revision 17

8-22 Revision 10 2-61 Revision 17
4-44 Revision 11 2-64 Revision 17
2-54 thru 2-55 Revision 12 xvi Revision 18
9-1 thru 9-7 Revision 12 1-4 thru 1-5 Revision 18
9-14 and 9-24 Revision 12 2-38 Revision 18
iii thru vii Revision 13 2-57 thru 2-58 Revision 18
1-3 Revision 13 3-18 thru 3-27 Revision 18
2-2 and 2-5 Revision 13 3-42 Revision 18
2-28 thru 2-47 Revision 13 5-3 Revision 18
2-65 thru 2-70 Revision 13 8-8 Revision 18
2-86 and 2-95 Revision 13 9-2 and 9-8 Revision 18
2-97 and 2-100 Revision 13 9-13 thru 9-14 Revision 18
2-105 thru 2-111 Revision 13 10-3 Revision 18
3-11 thru 3-15 Revision 13 2-65 Revision 19
4-12 thru 4-23 Revision 13 2-69 Revision 19
4-28 Revision 13 2-72 Revision 19
5-12 thru 5-14 Revision 13 3-12 Revision 19
7-14 and 7-29 Revision 13 3-16 Revision 19
8-2 and 8-22 Revision 13 7-14 Revision 19
9-3, 9-7 and 9-27 Revision 13 9-8 Revision 19
10-7 thru 10-9 Revision 13
2-3 and 2-7 Revision 14
3-18 and 3-38 Revision 14
4-4 and 4-6 Revision 14
7-14 and 7-29 Revision 14
8-1, 8-7 to 8-10 Revision 14
9-2 thru 9-3 Revision 14
9-7 thru 9-8 Revision 14
9-13 thru 9-14 Revision 14
9-23 Revision 14
2-7 Revision 15
2-47 and 2-48 Revision 15
2-63 and 2-66 Revision 15
2-94 and 2-95 Revision 15
2-116 Revision 15
4-94 Revision 15
5-13 Revision 15
8-7 and 8-8 Revision 15
8-26 Revision 15
9-3 Revision 15
9-15 Revision 15
2-23, 2-27, and 2-35 Revision 16
9-2, 9-5 thru 9-6 Revision 16
9-16 and 9-22 Revision 16

xv
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

TABLE OF CONTENTS
Chapter Page

1 BEFORE YOU START 1-1

SECTION 1 – INTRODUCTION 1-1

SECTION 2 - OBJECTIVE AND SCOPE OF THIS MANUAL 1-1
2-1 Installation Plan 1-1
2-2 Interconnection 1-1
2-3 Presentation 1-1
SECTION 3 - ON-SITE REQUIREMENTS 1-2
3-1 Tools and Test Equipment 1-2
3-2 Documentation 1-2
3-3 MIS Maps 1-2
SECTION 4 - DESCRIPTION OF SYSTEM 1-3
SECTION 5 – LOCK-OUT & TAG-OUT (LOTO) 1-4

2 PHYSICAL INSTALLATION 2-1

SECTION 1 - PHYSICAL INSTALLATION SEQUENCE GUIDE 2-1
SECTION 2 - INSTALLATION JOB CARDS 2-5

3 SYSTEM UPGRADE OR REPLACEMENT 3-1

SECTION 1 – TABLE OF JOBCARDS CONTENTS 3-1
SECTION 2 – JOBCARDS CONTENTS 3-2

4 CALIBRATION AND CONFIGURATION 4-1

SECTION 1 – TABLE OF JOBCARDS CONTENTS 4-1
SECTION 2 – JOBCARDS CONTENTS 4-3

5 FUNCTIONAL CHECK 5-1

SECTION 1 - INTRODUCTION 5-1
SECTION 2 - TOOLS AND TEST EQUIPMENT 5-2
SECTION 3 – SYSTEM POWER UP 5-2
SECTION 4 – TABLE 5-3
SECTION 5 – WALL STAND, SG100 WALL STAND, AND SG120 WALL STAND 5-5
SECTION 6 – CASSETTE TRAY 5-15
SECTION 7 – OTS SUSPENSION 5-15
SECTION 8 – JEDI GENERATOR 5-16

xvi
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

TABLE OF CONTENTS (CONT.)

Chapter Page
6 JEDI GENERATOR THEORY AND FUNCTIONAL DESCRIPTION 6-1
SECTION 1 – THEORY OF OPERATION 6-1
SECTION 2 – THEORY PRESENTATION 6-3

7 EXCEPTION HANDLING AND ERROR CODES 7-1

SECTION 1 - TABLE 7-1
SECTION 2 – JEDI EXCEPTION HANDLING 7-5
SECTION 3 – ERROR CODE, DIAGNOSTICS & TROUBLESHOOTING 7-9

8 PLANNED MAINTENANCE 8-1

SECTION 1 – PREVENTIVE MAINTENANCE ACTION LIST 8-1
SECTION 2 – PREVENTIVE MAINTENANCE JOB CARDS 8-4

9 RENEWAL PARTS 9-1

SECTION 1 – PROTEUS XR/a SYSTEM RENEWAL PARTS LIST 9-1
SECTION 2 – JEDI GENERATOR RENEWAL PARTS 9-29
SECTION 3 – JEDI GENERATOR DISASSEMBLY/REASSEMBLY 9-37

10 SCHEMATICS 10-1
SECTION 1 – PROTEUS XR/a SYSTEM MIS MAP 10-1
SECTION 2 – JEDI GENERATOR ILLUSTRATIONS 10-25
SECTION 3 – JEDI GENERATOR CENTRAL LISTING 10-50
SECTION 4 – OTS CONSOLE ILLUSTRATIONS 10-62

xvii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

xviii
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 1 BEFORE YOU START

SECTION 1 INTRODUCTION

The goal of this document is to guide the service representative through an entire
X-ray room installation.
The following On-site Requirements must be accounted for prior to beginning
installation of the system.

SECTION 2 OBJECTIVE AND SCOPE OF THIS MANUAL

This direction will lead you in a correct sequence through the manuals needed to
install the equipment. Following the suggested sequence will result in an orderly
installation. However, extenuating circumstances may dictate a deviation from the
recommended sequence. Feel free to deviate, but keep track of your progress by
checking off the tasks in the flowchart as you complete them.

Check equipment according to the packing list (Product Delivery Instructing) for
your system against the main catalog numbers in the “System Listing Chart.” Also,
verify that all manuals are present in the binders according to the Table of
Contents.

All interconnection cables are furnished in variable, preselected lengths from the
“Cable Data Packet.” Before starting to install your system, identify all the cables
and check their length to verify that they are long enough. If you find a short cable,
contact us immediately so we can send the required length cable to you and
thereby, not delay the installation.

2-1 Installation Plan

The main steps in the installation plan are easily seen by looking at the Table of
Contents for this document. The plan objectives are to:

1. Give a logical installation order which recognizes mechanical and electrical

interface areas
2. Test and adjust each subsystem independently.

To obtain a good overall view of how these objectives are to be achieved review
the Table of Contents for this document before beginning the installation work.
Then, if it is necessary to deviate from the stated plan, you will be aware of the
essential interface areas. This will give you the information required to make
another effective plan which applies to our particular situation.

2-2 Interconnection
Interconnection of products by furnished cables or contractor supplied wiring is
indicated by numbered MIS runs in the installation sections. Run interconnect
charts are available which describe the connection and function of each wire.

For Proteus XR/a system, refer to the following:

• Proteus XR/a system Cable Maps (Chapter 10)

2-3 Presentation
The procedures in this steering manual are presented in job card form.

1-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 3 ON-SITE REQUIREMENTS

3-1 Tools and Test Equipment

There are additional tools and test equipment besides the standard service
representative tool kit which must be available before installing the Proteus XR/a
System. Refer to each subsystem service manual for details.

3-2 Documentation

Directions are necessary for correct installation of the Proteus XR/a system.
Procedures from each document will be used and reflect the latest information
available at this time.

Not all procedures in this manual apply to all sites. Before you begin installation,
cross out the procedures that do not apply to your site.

3-3 MIS Maps

The proper system cable interconnect map is necessary for correct installation of
a Proteus XR/a system. Refer to:

• Proteus XR/a system MIS Maps (Chapter 10)

1-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 4 DESCRIPTION OF SYSTEM

Illustration 1-1
BASIC CONFIGURATION

7
8

9 / 10

1 2

The Proteus XR/a System is divided in to basic components:

1. System Console 7. Generator Cabinet
2. Elevating Table 8. X-ray Tube
3. XT radiographic Suspension 9. Proteus XR/a Collimator
4. Wall Stand (GPCP No.: 2260354) 10. Eclipse Proteus Collimator
(optional) (GPCP No.: 2379827)
6
5. SG100 Wall Stand (GPCP No.: 11. Tomography (optional)
2225849) (optional)
6. SG120 Wall Stand (GPCP No.: 12. Printer (optional)
2402562) (optional)

1-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 5 LOCK-OUT & TAG-OUT (LOTO)

3-1 System Power

Name Of Equipment: Proteus

Number Of Locks: One per person, working on the system
Title(s) of Employees Authorized to Perform LOTO:
Those trained in Lockout Tagout (LOTO)
Title(s) of Affected Employees and How to Notify:
Hospital Personnel; notified by verbal communication.

Energy Source Yes No Location of Energy Magnitude of

Isolating Means Energy
Electrical X System’s Main “A1” 320-480VAC,
Power Disconnect 3 Phase
Pneumatic X
Hydraulic X
Gas/Water/Steam X
Chemical X
Mechanical Motion X
Motion X
Gravity X
Springs X
Thermal X
Stored Energy X
Air Under Pressure X
Oil Under Pressure X
Water Under Pressure X
Gas Under Pressure X
Steam X
Other X

Type(s) of Equipment and/or Method(s) Selected to Dissipate or

Isolate Stored Energy:
Allow 3 minutes for stored energy to dissipate.

Type(s) of Equipment and/or Method(s) Used to Ensure

Disconnection’s:
One Lock & Tag for Main “A1” Disconnect.

1-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-2 LOTO Procedure for System Power

Name Of Equipment: Proteus

Step Lockout/Tagout Procedure

1 Prepare for shutdown of equipment by notifying affected personnel
working in the area that lockout/tagout is being performed.
2 Bring system software down.
3 Locate main power supply (Service) disconnect feeding System Cabinet.
4 Lock Out / Tag Out the main power disconnect.
5 Using an insulated voltmeter, measure the incoming power connection to
the system cabinet at the circuit breaker.
6 If no voltage is present at the system cabinet’s circuit breaker; place the
power switch on the PDU to the OFF position and service equipment as
required.
7 After service has been performed, notify affected personnel that
equipment will be reenergized and LOTO devices are being removed.
8 Assure the safety of the area and that all safety devices and guards have
been replaced.
9 Return system functions to a preset state.
10 Remove Lock-Out Tag-Out equipment from main disconnect.
11 Locate main power supply (Service) disconnect feeding System Cabinet
and re-apply power.

1-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

1-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 2 PHYSICAL INSTALLATION

SECTION 1 PHYSICAL INSTALLATION SEQUENCE GUIDE

Each system is installed in the sequence that will insure the safest and most time
efficient installation. The installation sequence performed at most sites is as
follows:

DONE
RECEPTION
STEP CHECK, PERFORM IST 001 JOB CARD
1 UNPACKING

ASSEMBLE
STEP OTS PERFORM IST 002 JOB CARD
2 CARRIAGE

CONNECT
STEP PERFORM IST 003 JOB CARD
OTS CABLES
3

POSITIONING
STEP PERFORM IST 004 JOB CARD
THE TABLE
4

MOUNT
STEP PERFORM IST 005 JOB CARD
GRID
5

INSTALL
STEP PERFORM IST 006 JOB CARD
TABLE TOP
6

PERFORM IST 007 JOB CARD

FOR WALL STAND
(GPCP No. 2260354)(optional);

STEP PERFORM IST 008 JOBCARD

INSTALL FOR SG 100 WALL STAND
7
WALL STAND (GPCP No. 2225849)(optional);

PERFORM IST 009 JOBCARD

FOR SG120 WALL STAND
(GPCP No. 2402562)(optional).

2-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

MOUNT
STEP SYSTEM PERFORM IST 010 JOB CARD
8 CONSOLE &
PRINTER

WARNING
STEP SIGNS AND PERFORM IST 011 JOB CARD
9 LABELS

PERFORM IST 012 JOB CARD

FOR RAD 14,21 X-RAY TUBE
MOUNT X-RAY
STEP
TUBE
10
PERFORM IST 013 JOB CARD
FOR MX100 X-RAY TUBE

PERFORM IST 014 JOB CARD

MOUNT FOR RAD 14,21 X-RAY TUBE
PROTEUS
XR/A
COLLIMATOR PERFORM IST 015 JOB CARD
FOR MX100 X-RAY TUBE

STEP
OR
11

PERFORM IST 016 JOB CARD

MOUNT FOR RAD 14,21 X-RAY TUBE
ECLIPSE
PROTEUS
COLLIMATOR PERFORM IST 017 JOB CARD
FOR MX100 X-RAY TUBE

PERFORM IST 018 JOB CARD

FOR RAD 14,21 X-RAY TUBE
ASSEMBLE
STEP
TUBE COVER
12
PERFORM IST 019 JOB CARD
FOR MX100 X-RAY TUBE

ELECTRICAL
STEP PERFORM IST 020 JOB CARD
CONNECTIONS
13

2-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

ALIGN TABLE
STEP BUCKY WITH PERFORM IST 021 JOB CARD
14 COLLIMATOR

ALIGN WALL
STEP BUCKY WITH PERFORM IST 022 JOB CARD
15 COLLIMATOR

MOUNT
STEP ANCHOR PERFORM IST 023 JOB CARD
16 BOLTS

TOMO-LINK
STEP PERFORM IST 024 JOB CARD
ASSEMBLY
17

INSTALLATION
STEP PERFORM IST 025 JOB CARD
CHECK
18

APPLY
STEP SPANISH PERFORM IST 033 JOB CARD
19 LABELS

Note: If your country requires the product rating plate label to be in the
language of that country, follow the instructions on document
#45474336. Paste the appropriate language label over the English
rating plate. The rating plate labels are: 2379361 (Spanish),
2379361-2 (German), 2379361-3 (French), 2379361-4 (Italian).

Note: Spanish Label Kit (2382506), Focus Label (46-23972P2), and Console Label
(610-3089) are in the OPEN ME FIRST box in Crate #4-6.

2-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank.

2-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2 INSTALLATION JOB CARDS

PROTEUS XR/A 1/2 IST 001

Subassembly: Reception Check, Unpacking

Purpose: Prepare for installation Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 2
From / / From Time: 2h
To / / To
1. Pre-installation Check

1) Verify all required cable ductwork, conduits, and raceways are installed according to Site Plans. Ensure
Customer supplied cables/wires are in place for connection to the system.

• Ensure that High Voltage and power cables are separated from signal cables as
much as possible.
• Verify that 3-phase power and ground lines can be placed in the same trough or
conduit.

2) At this time, the “Sales/Service Pre-installation Checklist,” provided in the applicable planning direction,
should be reviewed and signed off by the salesman and the Service Department representative.

Mark exact positions of components on the floor, wall and/or ceiling.

2. Unpacking

The PROTEUS XR/a system is shipped in four crates to facilitate transport and installation. Crates
dimensions and weights are shown in Table 1-1 below.

Crate dimensions & weight

Content Length Width Height N.W. G.W.
mm mm mm kg kg
Table Top and 1065 1100 2410 200 350
Base
Cabinet 1955 690 790 150 200
Wall Stand 620 800 2360 100 250
(GPCP No.
2260354)
(optional)
SG100 Wall 880 840 2280 186 280
Stand (GPCP No.
2225849)
(optional)
SG120 Wall 940 890 2410 220 300
Stand (GPCP No.
2402562)
(optional)
Accessories 1270 1100 1220 50 120

2-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/2 IST 001

• Do not discard any packing material such as envelopes, boxes, bags until all parts
are accounted for against the packing list.

• Check the mechanical condition and external appearance of all parts for possible

• damage or missing items.

• The distribution center or factory must be notified immediately of any damage or

shortage of parts.

Note: Do not use the capacitors in the Accessories crate #4 for installation. Please pay attention to pick
out and dispose the capacitors in the Accessories crate #4. Ensure the eco-friendly disposal of
the capacitors.

2-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/5 IST 002

Subassembly: Assemble OTS Carriage

Purpose: Installation Procedure Version no. 1
Date: 25/07/05
NF No. Production date Serial No. Personnel: 2
From / / From Time: 4hour
To / / To

1. Install the Stationary Rails according to the procedure

outlined in Direction 46-019639, Advantx XT Stationary Rails
Installation & Adjustments.

2. Unpacking
Remove Cardboard box and wood shipping support.
Cardboard &
Wood shipping
support

Note: If the system is equipped with TOMO link, please

insert the two TOMO driver cables (2124056 and
2132261) into the cable drape hose before lifting the
OTS bridge into position. Refer to Job card IST 025 on
page 3-25.

3. If the system is equipped with a Siemens Manual Collimator

(2259989), replace the existing field light transformer on top of
the OTS carriage with the 2143622-2 transformer provided with
catalog S3918KP. Re-use the existing mounting hardware.
Refer to OTS service manual for transformer location and
replacement, Refer to CAL 015 to calibrate lamp voltage.

2-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/5 IST 002

4. Install Overhead Bridge onto Shipping Dolly.

Bolt Bridge Carriage to Overhead Bridge

Note: The six bolts must be installed and tightened.

Be extremely careful not to pinch cables between

dolly & carriage when tightening bolts.

5. Remove the eight bolts from the front crosstie.

Move the crosstie towards bridge center about 10cm.

6. Remove the six shipping bolts on both sides of Carriage.

On both sides

2-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/5 IST 002

7. Attach OTS Lifting Fixtures A to Overhead Rails

Fixture position refers to Direction 46-019803 Advantx VHLZ

XT Inboard Suspension Installation.

8. Attach OTS Lifting Fixtures B to Overhead Bridge

Note: Make sure the crank handles are both on the

same side of the bridge.

On both

9. Route the straps outside of bridge rail.

Attach the strap ends to OTS Lifting Fixtures A on Overhead

Rails.

Note: The bolts should be fastened.

2-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 4/5 IST 002

10. Rotate the two cranks on Lifting Fixtures B on Overhead

Bridge evenly to raise the Carriage.

With OTS partially raised, remove 2 metal shipping brackets

(both sides of Carriage), 4 bolts each.

11. Remove metal Shipping Brackets.

Note: Make sure the crank handles are both on the

same side of the bridge.

Be extremely careful not to pinch cables between

dolly & carriage when tightening bolts.

2-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 5/5 IST 002

12. Bridge Installation

a) Raise bridge up to stationary rails with cables hanging to

the floor. Place bearings of rear crosstie into rear
stationary rail.

Gently move Overhead Bridge until bearings fall into

bearing track in Aluminium rail.

b) Place the front crosstie into position on bridge and bolt the
crosstie to the bridge.

c) Center front and rear crosstie bearings on wearstrips and

tighten eight screws securing front crosstie to bridge.

Note: Be sure bearings ride on the center of the

wearstrips over the complete range of OTS travel.
If bearings travel off center, the stationary rails
and crosstie alignment must be checked.

d) Lower bridge until roller bearings contact wearstrips.

e) Remove Lifting Fixtures B from the bridge and lower to

the ground.

f) Adjust upper bearings on both crossties for .02 gap to

upper part of rails. (Adjustment made with Allen wrench
from bottom of crosstie)

g) Remove Lifting Fixtures A from the stationary rails.

2-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 003

Subassembly: Connect OTS Cables on Carriage Side

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / / From Time: 10min
To / / To

1. Connect OTS Console locks power cable (2258381;for

MX100 tube, apply cable 2378475). Refer to system
MIS chart in page 10-1.

Note: The OTS I/F PCB PWR Supply cable

(2268131) is factory connected.
2268131

2258381/2378475

2. Connect cables to OTS control board. (J1, J101, J4,

J3, J100, J6). Refer to system MIS chart on page 10-1
and Job card IST 020 in this Chapter.

3. Connect Collimator Power & CAN cable (2258383),

OTS Console Power & CAN cable (2259867; for
MX100 tube, apply cable 2378473), OTS CAN cable
(2258389 or 2258389-2), and AC power cables. Refer
to system MIS chart on page 10-1 and Job card IST
020 in this Chapter.

2-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/2 IST 004

Subassembly: Positioning the Table

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 4
From / / From Time: 20min
To / / To

1. Turn the handle clockwise to lift table base.

2. Mount the trolley wheels on the bracket and fasten the four
screws.

Note: The trolley wheels are in box 1-7.

3. Turn the handle counter-clockwise to make the wheel load

the table weight.

4. Take off the wood stoppers. Then take out the shipping base.

5. Rotate the four trolleys wheels to parallel position with table

longitudinal axis.

Don’t put your feet under the table base.

CAUTION The table is very heavy and may hurt you.

2-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/2 IST 004

6. Position the table as close as possible to the center of the

collimator light field.

Note: When positioning the table base, ensure that the

minimum clearance on either side of the table from
the table base center to the wall is 3600mm:

If the room dimension is smaller than the specified

size, mount the table top before positioning the
table.

3600 3600

7. Repeat procedure (1).

8. Remove the trolleys.

9. Turn the handle counter-clockwise and put the table base on

the ground, then disassembly the trolley bracket.

2-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 005

Subassembly: Mount Grid

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / / From Time: 10 min
To / / To

1. Remove right side two metal tabs and keep left side metal Metal
tabs loose enough. tabs

2. Position the Ion grid evenly under the tabs.

3. Reinstall the removed tabs and fasten four screws.

4. Remove the shipping bracket.

5. Put the screws back on braking plate.

Note: These two screws are used to fasten braking
plate also. Must to be screwed.

6. Reinstall the table top.

2-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/2 IST 006

Subassembly: Install Table Top

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 2
From / / From Time: 10min
To / / To
Table Top Assembly/Installation
The following procedures describe how to install the table top on the table in those cases where removal is
required.

Table Top Installation

The table top is installed as follows:
1. Remove the end trim piece from one side of the table top
assembly. This consists of removing the two pan head screws,
which sit in the counter bores on the face of the trim piece.
End trim

2. Slide the table top assembly onto the bearing assemblies from one end.

Anti-collision
Note: Pay attention to the anti-collision
switches. Table top frame may collide
switch
with the switch.

3. Re-attach the trim to the table top assembly.

To obtain the smoothest and most quiet ride of the table top, adjustments may be made if necessary to the
table top bearings. These adjustments are made to precise specifications at the factory prior to shipping, but
shipping and handling may make minor “fine tuning” adjustments necessary after the table is assembled.

Note: Ensure that there is no lubricant, dust or other feculence on the slide rod.

2-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A TABLE TOP 2/2 IST 006

Table Top Adjustments

Note: Before adjusting, remove table top, then turn the table top around to opposite side. If the table
top still does not ride smoothly, proceed as follows:

While viewing the underside of the table top, move the table top back and forth. Check the bearings that ride
horizontally (eccentric bearings) for looseness or tightness. If eccentric bearings are loose, adjust eccentric
bearings out. If bearing is too tight, adjust eccentric bearings in.

Adjusting Eccentric Bearings Out

1. Remove end trim bracket.
2. Slide rail until eccentric bearing is visible.
3. Adjust eccentric bearing out using T-handle
Allen wrench.

Adjusting Eccentric Bearings In

1. Remove end trim bracket.
2. Slide rail until eccentric bearing is visible.
3. Adjust eccentric bearing in using T-handle Allen eccentric
wrench. bearing

Note: After the table is assembled, an operational

check is performed with adjustments made to
the Up/Down Limit Board if a correction in
table height is necessary (this check is
required only for the Elevating Tables).

2-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 1/2 IST 007

Subassembly: Install Wall Stand (GPCP No. 2260354)

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel:2
From / / From Time: 20min
To / / To

1. Remove the transport bolts of the counterweights. See

illustration.

2. Place the wall stand to proper position according to OTS.

Refer to page 4-4,4-5 in Proteus XR/a Pre-installation
manual for wall mount dimension and page 5-2, 5-3 in
Proteus XR/a Pre-installation manual for Room Layout.
3. Remove the transport block plates from wall stand rail top
end. See illustration. Transport
block

4. Remove the transportation clamps on both bucky rails.

Note: The content with a star is only for the wall stand
with a knee spacer. *
* Fix the carriage at a lower position.

2-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 2/2 IST 007

* Mount the Bucky and knee spacer assembly to the

carriage. *

* Fix the cables with the cable retainer.

*

* Mount the LAT bar.

Remove the protective cover on the knee spacer. Insert the
LAT bar into the hole, turn the flange to make the keys on the
flange insert the slots, then, lock the release bar.
Note: apply grease between the flanges.
*

* After the counter weight calibration, remove the foot cover,

tighten the anchor bolt in a proper position, reinstall the cover
finally.
*

THE WALL STAND IS HEAVY. AT LEAST TWO PERSONS ARE REQUIRED

TO MOVE AND ERECT IT TO PREVENT PERSONAL INJURY OR
EQUIPMENT DAMAGE.
THE FLOOR WHERE THE WALL STAND INSTALLED MUST BE FLAT AND
LEVEL TO PREVENT THE WALL STAND FROM FALLING DOWN.

2-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 1/8 IST 008

Subassembly: Install SG100 Wall Stand (GPCP No. 2225849)

Purpose: Installation Procedure Version no. 1
Date: 10/10/06
NF No. Production date Serial No. Personnel: 2
From / / From Time: 40 min
To / / To
THE SG100 WALL STAND MAY BE FACTORY SET FOR 110VAC OR 220VAC. THE
WARNING MISMATCH BETWEEN THE VOLTAGE SETTING OF SG100 AND THE POWER SUPPLY
VOLTAGE FROM SYSTEM PDU CAN RESULTS IN THE BROKEN POWER FUSE AND
LEAD TO THE FAILURE OF SG100 BUCKY. PAY ATTENTION TO CHECK AND
ENSURE THE SG100 WALL STAND LINE VOLTAGE AND BUCKY VOLTAGE TO BE SET
220VAC AND 230VAC RESPECTIVELY (SEE STEP 9,10 IN THIS JOB CARD) ON THE
INSTALL SITES BEFORE POWER ON.

THE WALL STAND IS HEAVY. AT LEAST TWO PERSONS ARE REQUIRED TO

MOVE AND ERECT IT TO PREVENT PERSONAL INJURY OR EQUIPMENT
DAMAGE.

Note: The floor where the Wall Stand installed must be flat and level to prevent the Wall Stand from
falling down.
Note: Before installing the SG100 Wall Stand, the X-ray tube supports and table must firstly be
installed.
Note: The procedures in this section are concerted with the revision 6 of SG100 Wall Stand Service
Manual (GPCP Number 2150297-100). For the reason of the update and change in that
manual, it is recommended to see also the latest Service Manual of SG100 Wall Stand for
reference.

1. Move the SG100, in the shipping container, to the installation area. (Refer to page 5-2, 5-3 in Proteus XR/a
Pre-installation manual for Room Layout). Leave the container in the horizontal position. Unpack the SG100
from the shipping container.

2. Using two people, carefully raise the SG100 to an upright position.

2-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 2/8 IST 008

3. Stand the SG100 against the wall and attach to the wall using the locally provided 6 wall anchors.
4. Align the SG100 laterally across the wall, to the X-ray Tube Suspension beam or table centerline using the
centerline marks on the wall and floor or the Laser Alignment Tool.

Note: The SG100 must be level on the wall with no more than 1/16 in. (1.5mm) deflection to
ensure that the anchors holding the SG100 to the wall does not come loose over time.
Use the shims provided with SG100 to ensure this requirement.

5. Verify the SG100 level across wall to ensure that no more than 1/16 in. (1.5mm) deflection exist, laterally or
vertically. See Illustration for recommended placement of the levels.
6. Insert supplied shims, as required, between the SG100 and the wall.
7. Tighten the six SG100 anchor bolts according to the torque specifications for the anchors.
8. Check the Counterweight and Bucky Carriage Counterbalance, and add or remove Counterweight when
required. (See SG100 Service Manual, GPCP Number 2150297-100)

2-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 3/8 IST 008

THE SG100 WALL STAND MAY BE FACTORY SET FOR 110VAC OR 220VAC. THE
WARNING MISMATCH BETWEEN THE VOLTAGE SETTING OF SG100 AND THE POWER SUPPLY
VOLTAGE FROM SYSTEM PDU CAN RESULTS IN THE BROKEN POWER FUSE AND
LEAD TO THE FAILURE OF SG100 BUCKY. PAY ATTENTION TO CHECK AND
ENSURE THE SG100 WALL STAND LINE VOLTAGE AND BUCKY VOLTAGE TO BE SET
220VAC AND 230VAC RESPECTIVELY (SEE STEP 9,10 BELOW) ON THE INSTALL
SITES BEFORE POWER ON.
9. Check the lock board jumper according to the table below to ensure the line voltage setting is 220VAC. Set
the TS-6 jumpers to 220VAC when necessary.
To access the lock board, remove the angulation support trim cover (behind the Bucky panel, at a 45 angle
facing the floor.). Remove the four screws. (See following Illustrations.)
The SG100 Wall Stand line voltage may be factory set for 110VAC or 220 VAC. Pay
CAUTION attention to check and ensure the line voltage to be set 220VAC on the install site via
jumper settings on its lock board.

Check and set the jumpers when necessary according to the following table:
LINE VOLTAGE Board: 45433412
TS-6 JUMPERS
220 VAC 2-3 & 4-5
110 VAC 3-5 & 4-6

2-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 4/8 IST 008

10.Set the Bucky voltage jumpers to the appropriate position for 230V. The Bucky voltage jumpers are
located next to the signal transformer in the electronic compartment behind the front panel (see
following illustrations).
The SG100 Wall Stand Bucky voltage may be factory set for 115VAC or 230 VAC.
CAUTION Pay attention to check and ensure the Bucky voltage to be set 230VAC on the install
site via Bucky voltage jumper.

To access this electronic compartment, turn the large knurled screws located underneath the front panel
counterclockwise. Tilt the front panel up and secure it with the prop on the right hand side. Then loosen,
without removing, the three flathead screws on the bottom of the lower panel, remove the two top roundhead
screws and slide the black cover plate up and out to access the jumpers.

220/110 Caution Label

Knurled
Screws-Loosen
to open Bucky
front panel

Lower Trim Covers

2-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 5/8 IST 008

11. Route and connect system cables to the I/O panel at the top of the SG100 (see table below).
Cable Name Cable SG100 end (stick to connectors on Other end
Part the I/O panel at the top of the
Number SG100) (See illustration “SG100
connectors” below)
SG100 Ion Chamber Cable 2145642-2 J40 Jedi connector AEC2 (refer
to page 2-92 in Job Card
IST 020 “Electrical
Connections”)
SG100 Auto Tray Cable 2145644-2 J41 System I/F Board
connector J124 (See
illustration “System I/F
Board connector J124” in
next page)
SG100 Bucky Cable 2145641-2 J42 Jedi Wall Bucky (J6)
connector (refer to page
2-92 in Job Card IST 020
“Electrical Connections”)
SG100 Power Supply 2151729-2 Power (See illustration “SG100 PDU connector TM4
Cable connectors” below) SG100 Power (See
illustration “PDU connector
TM4 SG100 Power” in next
page)
SG100 Ground Cable 2140362-2 Ground PDU ground

Illustration : SG100 connectors

Connect the two

black wires of
SG100 Power
Supply Cable into
these two
connectors.

2-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 6/8 IST 008

Illustration: System I/F Board connector J124

J124

Note: Pay attention to ensure the marked side of the

cable plug to face to you when connecting.

Illustration: PDU connector TM4 SG100 Power

TM4 SG100 Power

12. Attach the self-adhesive height correlation scale to the SG100 Wall Stand so it corresponds with the height
scale on the x-ray tube hanger or stand.

2-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 7/8 IST 008

13. Perform Microswitch Adjustment (Automatic Collimator Option only)

Five microswitches indicate the position of the Bucky (Refer to illustration below). The microswitch activator
cams for S4 (upper, near discrete SID point) and S5 (lower, far discrete SID point) may need slight
adjustment at installation time.
Microswitches S4 and S5 are located in the vertical brake assembly on the side opposite to the vertical lock
handle. The activator cams for microswitches S4 and S5 are located on the vertical column. Verify that the
activator cams actuate S4 and S5 as described below:
Note: This operation is carried out with the Bucky angulated to full horizontal position
Check that the activator cam for microswitch S4 actuates S4 when the Bucky is at the same level as the top of
the x-ray table (near discrete SID point). Reposition the cam actuator if necessary.
Check that the activator cam for microswitch S5 actuates S5 when the Bucky is in the lowest vertical position
(far discrete SID point) with the foldable legs extended and touching the floor. Reposition the cam actuator if
necessary.

Note: Vertical Bucky Wall Stand not equipped with the automatic collimator option do not have
positioning microswitches.
Check and ensure the parameter value in System Console to be the same with the actual distance between
Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low POS. distance”,
Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High Auto
CAUTION Exposure position set in System Console (see parameter 9 “High, low POS. distance”,
Job Card CAL 002) is 40cm, which is different from the default distance set on SG100
Wall Stand (44cm). So it’s a must to check and ensure the parameter value in System
Console to be the same with the actual distance between Low Auto Exposure position
and High Auto Exposure position when performing the SG100 SID calibration (refer to
Job Card CAL 006 in Chapter 4), even if the positions of the Microswitch S4 Activator
Cam and Microswitch S5 Activator Cam are not modified and be on the default position
in the upper step.

2-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 8/8 IST 008

14. Warning and Specification Labels

Warning labels are shipped with the SG100 for the foldable legs. The labels are written in three languages:
English, French and Spanish.
Locate the warning labels and attach the label of the appropriate language to the right-side folder leg (leg with
lock release knob).
Specification labels in four languages (French, German, Italian, Spanish) are shipped for adapting the SG100
specification label to the corresponding language where the SG100 is installed. The original specification
label, located in the upper lock-handle side of the vertical column, is in English.
If necessary, locate the specification label and attach the label of the appropriate language over the original
specification label.
15. Verify the Bucky grid speed setting.
The Bucky (Medys) must be set for Super speed using a 36L/cm grid. Normally this is done at the factory.
Verify that the switches are correctly set and if necessary change their settings, refer to the procedure in Job
Card LJS02 “SG100 VERTICAL BUCKY STAND MEDYS BUCKY SWITCHES” of SG100 Service Manual
(GPCP No. 2150297).

2-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 1/22 IST 009

Subassembly: Install SG120 Wall Stand (GPCP No.: 2402562)

Purpose: Installation Procedure Version no. 2
Date:10/10/06
NF No. Production date Serial No. Personnel: 2
From / / From Time: 40 min
To / / To

1. Unpacking
SG120 is shipped in one crate to facilitate transport and installation.
1) Move SG120, in the shipping container, to the installation area. Leave the container in the horizontal
position.
2) Remove the banding and cardboard box that is covering the equipment and clamped to the wooden pallet.
3) Remove the shipping wooden crosspieces holding SG120 to the pallet.
4) Rest the bottom end of SG120 on soft support material outside the shipping container.

2. Standing
1) Before standing, remove the top cover to ensure the pulley chains are on their sprockets. If they are not,
try to set the chains on the sprockets. USE CAUTION.
If the problem cannot be easily corrected, SG120 must be returned as DOA.
2) Using two people, carefully raise SG120 to upright position.

INJURY HAZARD! AT LEAST TWO PEOPLE ARE REQUIRED TO TURN OR TILT SG120.
WARNING SG120 WEIGHS APPROXIMATELY 180 KG (330 LBS) AND CAN EASILY BE TIPPED OR
UNBALANCED.

3. Floor mounting
Tools required:
- Standard service person tool kit
- Drill template
- Wrench set
- Laser alignment tool

2-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 2/22 IST 009

Procedure:
1) Using the drill template supplied with the equipment (included in installation kit), set the position of SG120
taking into account.

- The distance focal dependant to the anti-diffusion grid.

- The minimum recommended distance to the wall indicated on the drill template.
2) Place and align SG120 drill template laterally using the collimator light or the laser alignment tool.
3) Mark the holes using the template.
Note: Set the template to the floor means of adhesive tape to avoid it can be displaced.
4) Remove the template.
5) Drill the holes and place the anchors.
6) Using two people, carefully raise SG120 to upright position and move to the mounting location. Install the
anchor bolts.
7) Level the equipment using the 3 levelling screws and tight the anchor bolts.

Levelling screws

Note: Tightness that anchors need to set to is 50 Nm.

8) Recheck the alignment of SG120.

2-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 3/22 IST 009

Note: SG120 Vertical Bucky Stand can be either LEFT or RIGHT loaded. The equipment is
factory LEFT handed configured. The procedure to change the configuration follows.
MAKE SURE THE EQUIPMENT IS SWITCHED OFF DURING THIS OPERATION.
WARNING DURING THIS OPERATION, THE BUCKY CARRIAGE AND COUNTERWEIGHT
CARRIAGE CAN MOVE.
4. Bucky Reversal Procedure
1) Remove covers and panel
a. Remove the back covers from the bucky support assembly.

b. Remove the front panel from the bucky support.

2) Vertical lock handle

The handle is located on the left side of the bucky support assembly.

2-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 4/22 IST 009

a. Remove the plate below the bucky support assembly to access to the interface board.

Interface Board

b. Release the switch cable from the interface board, J8.

c. Remove with care the four screws that hold the handle.

d. Extract carefully the handle with the switch cable.

e. To assembly the handle on the new side, first remove the white plug for cable insertion and
the four screws.

2-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 5/22 IST 009

f. Pass the switch cable through the hole on the new side and fix the handle with the 4 screws.

g. Connect the switch cable to J8 on interface board and assembly the plate removed in step a
in 2) above.
3) Bucky assembly
To change the configuration of the bucky for the cassette tray insertion, follow the next procedure:
Note: There is some difference between with patient support and without patient support.
Please confirm whether you’ve installed patient support.
a. Extract the cassette tray with CAUTION. THE BUCKY CARRIAGE WILL MOVE UP.
b. Remove the bucky cover protecting the bucky electronic devices.

c. Remove the 8 white plugs (4 on each side) located on the back of the bucky support.
Note: Remove the 6 white plugs (3 on each side) located on the back of the bucky support,
for the other 2 on the top (1 on each side) are covered if the patient support option is
installed.

Four more
plugs on the
other side.

2-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 6/22 IST 009

d. Remove the 7 screws that hold the lateral cover of the bucky: 3 of them are situated on the
bucky frame and the other 4 are accessible from the back of the bucky support through the
holes left uncovered in the previous step.

Note: When the patient support option is installed, one of the 4 holes located on the back of
the bucky support (the one of the top on either side) is partially obstructed by the
magnets that are assembled with the patient support option. To access the four screws
from the back of the bucky support referred in step d, it is first needed to disassembly
the magnets that obstruct the holes.

e. Once the lateral cover is free, move it to the opposite side of the bucky to fix it. To enable the
displacement of the lateral cover, It is needed you cut the flanges that hold the cable to the
bucky frame.

2-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 7/22 IST 009

Note: Since the ion chamber is assembled to the bucky, you can temporary displace it to let
the lateral cover pass through the area between the bucky structure and the ion
chamber. For that, just loosen the screws that hold the ion chamber and move it in
order to facilitate the operation.

f. Guide the cable, making sure that you do not interfere with the internal bucky mechanism
and fix it with flanges to the bucky sheet metal frame.

2-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 8/22 IST 009

g. Make sure about the guiding of the cable. See below bucky for LEFT handed loading
(factory) and RIGHT handed loading.

MEDYS Bucky

cable

LEFT

cable
RIGHT

h. Fix the lateral cover to the opposite side with the 7 screws removed in step c in 3) above.
Note: When the patient support is installed, remember to fix the magnets removed in order to
be able to access the screws.
i. Insert again the 8 white plugs removed in step c.
Note: When the patient support is installed, there are 6 white plugs need to be insert.
j. Assembly the bucky cover removed in step b.
k. In the front panel, change the position of the cover to the opposite side.

Assembly this
cover on the
opposite side.

l. To finish, assembly the front panel and the back covers removed in 4. 1) (Remove covers
and panel) above.
m. Insert the tray using the new configuration.

2-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 9/22 IST 009

Note: Check the Counterweight and Bucky Carriage Counterbalance, and add or remove
Counterweight as following when required.

5. Counterweight and Bucky counterbalance check

Even though the bucky carriage is factory balanced this procedure must be carried out.
1) Remove the column lateral covers.
2) Insert the cassette tray in the bucky.

Cassette tray
insertion

3) Place a medium size cassette into cassette tray.

4) Loosen and remove the fixing square and retaining bar.

Pulley chains

Fixing square Retaining bar

5) Check that the counterweight and bucky carriage are well balanced:
- WITH POWER ON: Release the electromechanical brake and check the bucky carriage can
move easily in vertical direction.
- WITH POWER OFF: Check that the bucky carriage can move freely and smoothly in vertical
direction.

Note: The electromechanical brakes do not lock with power OFF.

If the counterweight and bucky carriage are not well balanced, follow the procedure
detailed below to add or remove counterweights.

2-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 10/22 IST 009

6. Adding or removing counterweights

DURING THIS OPERATION, THE BUCKY CARRIAGE AND COUNTERWEIGHT

WARNING CARRIAGE CAN MOVE.

1) Move the carriage to the lowest position.

2) Remove the metal cover on the front of the column.

Metal cover

3) Remove the second metal cover to access the counterweights.

Metal cover

Counterweights

4) Place or remove the counterweights with care.

5) Reinstall the two sheet metal covers and the column lateral covers.

7. Electrical Installation
1) Power cable connection
Power and ground cables are supplied optionally with the equipment.
a. Connect power supply cable from J1 VAC on the bucky control board.
b. Connect the ground cable to the ground stud on the bucky control board.
2) System cable connection
System Cable Connection (Code: 2145641-2, 2145642-2 and 2145644-2) is supplied optionally with SG120.

2-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 11/22 IST 009

a. Connect Bucky cable (Code: 2145641-2) to J42 on the bucky control board.

ENSURE THAT THE BUCKY IS SET CORRECTLY FOR THE GENERATOR VOLTAGE
WARNING (115VAC OR 230VAC). THE BUCKY IS SET FOR 115VAC OR 230VAC IN FACTORY TO
AVOID EQUIPMENT DAMAGED. PAY ATTENTION TO CHECK THE VOLTAGE, AND SET
JUMPERS BY REFERRING TO THE VOLTAGE CHANGE INSTRUCTIONS IN THE BUCKY
MANUAL.

b. Connect Ion Chamber cable (Code: 2145642-2) to J40 on the bucky control board.

c. Connect Sensing Tray cable (Code: 2145644-2) to J41 on the bucky control board.

Cable Name Cable SG120 end Other end

Part (stick to
Number connectors
on the I/O
panel at the
top of the
SG120)
SG120 Ion Chamber Cable 2145642-2 J40 Jedi connector AEC2 (refer to page 2-94 in Job
Card IST 020 “Electrical Connections”)
SG120 Auto Tray Cable 2145644-2 J41 System I/F Board connector J124 (See illustration
“System I/F Board connector J124” in next page)

2-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 12/22 IST 009

Cable Name Cable SG120 end Other end

Part (stick to
Number connectors
on the I/O
panel at the
top of the
SG120)
SG120 Bucky Cable 2145641-2 J42 Jedi Wall Bucky (J6) connector (refer to page 2-94
in Job Card IST 020 “Electrical Connections”)
SG120 Power Supply Cable 2410108-2 Power PDU connector TM4 SG120 Power (See illustration
“PDU connector TM4 SG120 Power” in next page)
SG120 Ground Cable 2140362-2 Ground PDU ground

Illustration: System I/F Board connector J124

J124

Note: Pay attention to ensure the marked side of the

cable plug to face to you when connecting.

Illustration: PDU connector TM4 SG120 Power

TM4 SG120 Power

2-39
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 13/22 IST 009

8. Perform Microswitch Adjustment (Automatic Collimator Option only)

Five microswitches indicate the position of the Bucky (Refer to illustration below). The microswitch activator
cams for S4 (upper, near discrete SID point) and S5 (lower, far discrete SID point) may need slight
adjustment at installation time.
Microswitches S4 and S5 are located in the vertical brake assembly on the side opposite to the vertical lock
handle. The activator cams for microswitches S4 and S5 are located on the vertical column. Verify that the
activator cams actuate S4 and S5 as described below:
Note: This operation is carried out with the Bucky angulated to full horizontal position
Check that the activator cam for microswitch S4 actuates S4 when the Bucky is at the same level as the top of
the x-ray table (near discrete SID point). Reposition the cam actuator if necessary.
Check that the activator cam for microswitch S5 actuates S5 when the Bucky is in the lowest vertical position
(far discrete SID point) with the foldable legs extended and touching the floor. Reposition the cam actuator if
necessary.

S4 BEHIND COVER PLATE

S5 BEHIND COVER PLATE

Microswitch S4 activator cam

Microswitch S5 activator cam

Note: Vertical Bucky Wall Stand not equipped with the automatic collimator option do not have
positioning microswitches.

2-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 14/22 IST 009

Check and ensure the parameter value in System Console to be the same with the actual distance between
Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low POS. distance”,
Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High Auto
CAUTION Exposure position set in System Console (see parameter 9 “High, low POS. distance”,
Job Card CAL 002) is 40cm, which is different from the default distance set on SG100
Wall Stand (44cm). So it’s a must to check and ensure the parameter value in System
Console to be the same with the actual distance between Low Auto Exposure position
and High Auto Exposure position when performing the SG120 SID calibration (refer to
Job Card CAL 006 in Chapter 4), even if the positions of the Microswitch S4 Activator
Cam and Microswitch S5 Activator Cam are not modified and be on the default position
in the upper step.

9. Warning and Specification Labels

Specification labels in seven languages (Spanish, English, French, German, Portuguese, Chinese and
Japanese) are shipped for adapting the SG120 specification label to the corresponding language where the
SG120 is installed. The original specification label, located in the upper lock-handle side of the vertical
column, is in English.
If necessary, locate the specification label and attach the label of the appropriate language over the original
specification label.

10. Verify the Bucky grid speed setting.

The Bucky (Medys) must be set for Super speed using a 36L/cm grid. Normally this is done at the factory.

2-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 15/22 IST 009

11. Covers assembly

1) Bucky covers
The bucky covers (1 front cover + 2 rear covers) of the SG120 are factory assembled. Only the next
procedure has to be carried out:

There are cutting operations to be made on some pre-cut areas in most of the types of
CAUTION SG120 covers.
The cutting operation has to be carried out with CAUTION to avoid personal injury or
damage to the cover.
It is not recommended to carry out the cutting work in only one step, but to repeat the
cutting operation carefully and as many times as necessary until being able to remove
easily the cover part to reject.

a. Cut with an appropriate tool the pre-cut slot located on one of the sides of the front bucky
cover for cassette tray insertion. If you wish LEFT hand load, cut the left side of the cover; if
you wish RIGHT hand load, cut the right side of the cover.

Note: The equipment is factory LEFT handed configured, so the LEFT pre-cut side of the cover
should normally be cut, unless you want to inverse the tray insertion. If you wish to change
the hand load configuration, follow the procedure detailed in 4 above.

2-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 16/22 IST 009

Note: To disassembly the different bucky covers, loosen the screws shown below.

b. Connect the ground cable to the ground stud on the bucky control board.

2-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 17/22 IST 009

2) Column covers
The column frontal cover is assembled at factory. If you need to disassembly it, follow the next procedure:
a. Remove the screws (4 in total, 2 on each side) fixing the cover to the squares at the bottom
of the column.

b. Remove the 2 screws fixing the cover to the top of the column.

c. Move the bucky carriage assembly to the lowest position and remove the front cover with
care.
The column lateral and top covers are supplied disassembled into the packing box.

2-44
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 18/22 IST 009

The procedure to assembly the lateral and top covers follows:

a. Make sure the column front cover is assembled.
b. Cut the pre-cut window for system cables entrance located on the rear side of one of the
lateral covers, depending on the side from where the system cables entrance needs to be
made in your installation.

c. Assembly one of the lateral covers (2 screws) to the plate located on the column top.

d. Fix the lateral cover to the square located on the foot of the column (1 screw).

2-45
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 19/22 IST 009

e. Take the second cover and make it fits with the cover already assembled.

f. Fix the second lateral cover to the top and foot of the column (steps b and c).
g. Connect the ON/OFF led cable supplied with the equipment and assembly the top cover
(4 screws) to the plate on the top of the column.
Note: Some of the holes to fix the covers have some safe clearance enabling to adjust the
assembly in the best conditions.

2-46
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 20/22 IST 009

12. Rotation limit screw

a. Localize the Switches S2-1 and S2-2 behind the back bucky support. See Figure Switches S2-1 & S2-2
localization.
b. Loose the S2-1 screws 1, 2, 3 (Figure Switch S2-1) with an Allen wrench number 3.
c. Loose the Limit rotation Screw with an Allen wrench number 4.
d. Take apart the Limit rotation Screw and put in the original position the Switch S2-1 by tighten the S2-1
screws 1, 2, 3.
e. Loose the S2-2 screws 1, 2, 3 (Figure Switch S2-2 & Screws) with a Allen wrench number 3.
f. Tight the Limit rotation Screw (Allen wrench number 4).
g. Put the Switch S2-2 in the original position by tighten the S2-2 screws 1, 2, 3.
Note: In Figure Switch S2-2 & Screws and Figure Switch S2-1 are shown the switch S2-1 & S2-2
without the microswitch only for clarification. Do not touch the electronic component. Only
is necessary to loose the screws as follows.

Figure Switches S2-1 & S2-2 localization

Note: Not to change this screw will cause that cassette tray falls when rotating.

2-47
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 21/22 IST 009

Figure Switch S2-1

Figure Switch S2-2 & Screws

WARNING THE LIMIT ROTATION SCREW SHOULD BE AT S2-1 WHEN LEFT HAND
CONFIGURATION, AND AT S2-2 WHEN RIGHT HAND. IN OTHER CASE THE
ROTATION (SEE FIGURE LEFT CONFIGURATION AND FIGURE RIGHT CONFIGURATION IN
SECTION 5-3-3-3) WILL BE DONE IN THE WRONG WAY AND THE CASSETTE TRAY WILL
SLIP WHEN ROTATING. HEEDING THIS WARNING MAY CAUSE INJURY TO THE
OPERATOR.

2-48
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A WALL STAND 22/22 IST 009

13. Covers for patient support option installation

Note: This item is applicable only if the patient support option kit is going to be installed. See
IST025 of this chapter.
In case the patient support option is going to be installed, the next procedure has to be followed for
NBS2100 covers:
a. Remove the back covers of the bucky support assembly.
b. Cut the pre-cut windows of the lower rear cover lodging the patient handgrips. Leave the cover ready for
further assembly.

c. Take the upper rear cover included in patient support option kit.
d. Cut the pre-cut windows of the upper rear cover (the one chosen in previous step) lodging the patient
handgrips. Replace the old upper rear cover by this new cover and leave it ready for further assembly.
e. Discard the old upper rear cover.
f. Follow the procedure described in IST025 of this chapter, referring to installation of patient support option.
g. Assembly the new upper and lower rear covers.

Figure: Look of rear bucky covers with Patient Support OPTION installed

2-49
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/7 IST 010

Subassembly: Mount System Console and Printer

Purpose: Installation Procedure Version no. 1
Date: 02/05/01
NF No. Production date Serial No. Personnel: 2
From / / From Time: 20min
To / / To

Note: There are three types of mounting available for each system. You should choose one according
to the system configuration and customer’s requirement.
Note: Connect the cables according to the job card IST 020.

1. Console with Pedestal

1-1 Mount the console plate (610-3081) on the console
pedestal.

610-3081

1-2 Mount the system console on the console plate and

fasten with the former screws.

1-3 Mount Hand Switch holder with the two screws.

2-50
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/7 IST 010

1-4 Connect console and cable.

Note: When you plug the console cable, make
sure lock the connector securely.

1-5 Mount Connecting Cover (610-3067).

610-3067

2. Console on the desktop

Note: There are tow choices to place console on the desktop.

2-a Only console on the desktop

2-a-1 Please select the Plug Cover Fixer (610-3113), shown as the
pictures below.
010-6006
610-3113

2-51
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/7 IST 010

2-a-2 Mount the part 610-3113 to the console.

Note: Console Surface PROTECTION!

2-a-3 Follow the steps 1-3,1-4,1-5.

2-b Console on the desktop with a bracket

2-b-1 Assemble Connecting Board (610-3091), Hand

Switch Fixing Plate (610-3068) and Bracket.

Note: There are two choices to assemble

610-3068 and 610-3091 according to
either the table or the wall you choose to
mount them on.

610-3068 610-3091

2-52
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 4/7 IST 010

2-b-2 Mount the assembly to console.

Note: Console Surface PROTECTION!

2-b-3 Follow the steps 1-3,1-4,1-5.

2-53
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 5/7 IST 010

3. Console mounted on the wall

3-1 Mark the mount holes onto wall using the bracket.
3-2 Drill two holes, and insert two M4 expanding bolts
into the wall.

3-3 Assemble Connecting Board (610-3091), Hand

Switch Fixing Plate (610-3068) and Bracket.
Note: The step is the same as the step 2-b-1, except
turning the connecting board (610-3091) 180°
and changing Hand Switch Fixing Plate
(610-3068) placement.

Note: Console Surface PROTECTION!

610-3091

3-4 Follow the steps 1-3,1-4,1-5.

3-5 Hang the bracket and console onto the bolts on the
wall.

2-54
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 6/7 IST 010

A printer is an optional component. Mount a system

console with a printer follows the steps below.
1. Remove the side cover from the system console.

2. Loosen or remove the screws.

3. Connect the system console and the printer with a cable.

4. Insert the printer into the system console.

5. Tighten the screws

2-55
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 7/7 IST 010

6. Mount a console plate.

Note: Choose a proper console plate according

to customer’s requirement.
If a table top mounting is chosen, follow
the step7, 8, 10, 11, 12.
If a pedestal mounting is chosen, follow
the step9, 10, 11, 12.

7. Assemble the bracket for table top mounting.

8. Mount the printer to the bracket.

9. Mount the printer to the pedestal, see step 1-1.

10. Insert the cable connector into the socket.

11. Mount the cable cover.

12. Follow the steps 1-3,1-4,1-5.

2-56
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/2 IST 011

Subassembly: Warning Signs and Labels

Purpose: Installation Procedure Version no. 2
Date: 10/10/06
NF No. Production date Serial No. Personnel:1
From / / From Time: 2min
To / / To

Warning Signs and Labels

Note: There four types of warning labels are delivered as accessories in “OPEN
ME FIRST” box.

2-57
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/2 IST 011

PROTEUS XR/A SYSTEM LABELS LOCATION

Note: Please select the appropriate warning label to affix it on

the right bottom of console.

WARNING LABELS SHOULD BE INCLUDED IN

WARNING “OPEN ME FIRST” BOX. IF THEY ARE MISSING,
PLEASE ORDER A NEW CONSOLE (2259976) IN
CONFORMITY WITH REGULATION
REQUIREMENTS.

2-58
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 012

Subassembly: Mount RAD 14,21 X-ray Tube

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 2
From / / From Time: 20min
To / / To
Note: This Job Card is only for RAD14,21 X-ray tube. For
the assembling of MX100 X-ray tube, please refer to
Job Card IST 013 in this Chapter.
1. Assemble tube bracket. Put the blue cover onto handle
if it is not assembled. Tube bracket
Note: Apply locktite to mount screws.

Note: For RAD 21 X-ray tube, there is no

trunion handle.

Upper
Clamp
Screws
2. Loosen the four screws of the upper clamp of tube
bracket.
3. Remove the upper clamp of tube bracket.
Screws
TO PREVENT THE CLAMPS FROM ANY IMPACT.
WARNING
IN CASE IMPACT OCCURRED, IT SHOULD BE
VERIFIED THAT THE CLAMP HAS ENOUGH
STRENGTH BEFORE INSTALLATION.

4. Put the X-ray tube on lower support of tube bracket.

5. Reinstall the upper clamp of tube bracket. Tighten four
screws surely.
Note: Pay attention to the marks on the clamps to put
the left and right clamps into proper position.
The torque applied to the four screws is 6.0~6.4
N.m.

6. Tube bracket has a trunion used to rotate the tube.

Loosen the two set screws and then adjust the lock nut
on both sides of the tube clamp. Make it lock the tube Lock Release
when moving the trunion forward and release the tube
otherwise.
7. Fasten the set screws again.
Note: For RAD 21 X-ray tube, there is no trunion handle, Lock
you just need to fasten clamp screws. Nut

2-59
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/2 IST 013

Subassembly: Mount MX100 X-ray Tube

Purpose: Installation Procedure Version no. 0
Date: 03/01/03
NF No. Production date Serial No. Personnel:2
From / / From Time: 20min
To / / To

Note: This Job Card is only for MX100 X-ray tube. For the assembling of RAD14, 21 X-ray tube, please
refer to Job Card IST 012 in this Chapter.
1. Assemble the lead cup (GPCP No.: 2379458) to the MX100 X-ray tube output window if the lead cup is not
attached before arrival at the install site.
BECAUSE OF THE POSSIBILITY OF IMPAIRMENT TO HUMAN HEALTH, PLEASE PAY
WARNING ATTENTION TO WEAR GLOVES AND PREVENT THE DIRECT CONTACT WITH HUMAN
BODY WHEN CARRYING OR ASSEMBLING THE LEAD CUP.
Note: The lead cup should only be applied with MX100 X-ray tube (GPCP No.: D2301R) and Auto
collimator GPCP No. 2259298-54 (or Manual collimator GPCP No. 2259989). Do not use Lead cup
with X-ray tubes or collimators of any other types, such as RAD14,21 X-ray tubes.
1) Clean the output window cover of MX100 tube.

Output
window

2) Remove the self-adhesive tape circle cover from the lead cup and attach the lead cup onto the output
window cover of MX100 tube. Apply pressure to attach tightly and ensure the fixation.

Remove the
self-adhesive Lead
tape circle cup
cover

2-60
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/2 IST 013

2. Attach the spacer to the tube as shown in illustration below with four hexagon socket head bolts (GPCP No.:
46-170498P11, see illustration). Apply locktite to each bolt. The flat side must be away from the tube output
window.

Mount these four bolts

to attach the spacer to Flat
the tube.

Tube
output
window

Note: Apply locktite to mount screws to ensure the firmly tube assembling.
Pay attention to the mounting direction of spacer. The flat side must be away from
CAUTION the tube output window.
3. Position the tube with spacer attached as shown in illustration below and secure them to the gooseneck with
four hexagon head bolts (GPCP No.: 001-4060-03, see illustration.). Apply locktite to each bolt.

Mount the four bolts (the

other two bolts are on the
other side of the
gooseneck.) to attach the
spacer to the gooseneck.

2-61
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 014

Subassembly: Mount Proteus XR/a Collimator to RAD 14,21 X-ray Tube

Purpose: Installation Procedure Version no. 2
Date: 20/6/06
NF No. Production date Serial No. Personnel:2
From / / From Time: 20min
To / / To

Note: This Job Card is only for RAD 14,21 X-ray tube. For the mounting of Proteus XR/a Collimator to
MX100 X-ray tube, please refer to Job Card IST 015 in this Chapter.
Note: For Manual Collimator, the transformer on OTS also needs replaced for proper lamp power supply,
please refer to Job Card IST002 and OTS service manual, after the collimator installation, please refer
to CAL 015 to calibrate lamp voltage.

1. Remove the three safety screws with red heads from the collimator (marked with white ellipses).

Transportation safety screw B

Collimator mounting screws

Transportation safety screw A

2. Check collimator aluminium plate quantity,if the collimator For RAD

has two pieces of plates installed, remove one and reserve 14,21 Tube,
only one piece of plate for RAD14,21 tube only
reserve
one piece of
Note: This action in step 2 is only for RAD14,21 Tube. plate
For MX100 Tube, do not remove any of the
Aluminium plate. (Refer to Job Card 015)

3. Loosen the three collimator mounting screws to their maximum permissible limit.
Remove all 3 transportation safety screws (marked with white ellipses), see
illustration A and B, before applying power to the collimator.
CAUTION
Before transportation tighten the transport safety screws A fully (they have to screw
in easily). Therefore the smallest x-ray field has to be set. For manual setting of the
collimator blades replace the left cover and adjust an opening of the collimator blades
of approx. 4.5 mm.
Turn off voltage before fitting or removing the cover.
Mind installation instructions and ESD regulations.

2-62
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/3 IST 014

4. Rotate the tube 180°.

5. Mount the collimator mounting flange and the OTS console

bracket with four provided screws.
Note: If the flange has been mounted in the factory, skip this step.
USE SOME MATERIAL TO PROTECT TUBE
WARNING WINDOW WHEN FASTENING SCREWS.
PAY ATTENTION TO THE DIRECTION OF
FLANGE. THE SLOT SHOULD BE ALIGNED
WITH OTS CONSOLE BRACKET.

Note: Apply locktite 242 to flange mount screws.

The force fastening screws is between 10~13 N.m.

6. Be careful not to damage the collimator fingers. Position the collimator on the X-ray tube. Be sure the detent
lever is not preventing the collimator from seating fully.
The collimator rotation lever must be fully depressed when mounting/installing the
CAUTION collimator to the mounting flange. Failure to do so could cause the collimator to mount
improperly and fall from the unit.
Note: Apply grease supplied to collimator mount flange and
collimator adapter for easy movement.

Apply grease Apply grease on

underneath the the inside surface Lever
flange edge of adapter

2-63
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/3 IST 014

7. Tighten the 3 collimator mounting screws in equal number of turns until they lock securely and can not be
turned anymore. Then back out each screw equally by maximum 1/2 turn, so that collimator can rotate freely
Verify that when the collimator is not in a detent location, the minimum rotate force is 20N.

8. Turn the X-ray tube back into

normal position.

CHECK THAT THE MOUNTING IS CORRECT

WARNING
BEFORE TURNING THE TUBE BACK TO NORMAL
POSITION.

BE SURE THAT THREE THRUST BUSHINGS

ARE SYMMETRIC TO THE CENTER AND HOLD
THE FLANGE FIRMLY.

9. Loosen the X-ray tube. Use level gauge to check that the
tube and collimator are in level position, and then fasten
the tube using trunion handle securely.
Note: For RAD 21 X-ray tube, there is no trunion handle.
Just need to fasten clamp screws.
Apply locktite to mount screws.
10. Mount the OTS Console.

2-64
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 015

Subassembly: Mount Proteus XR/a Collimator to MX100 X-ray Tube

Purpose: Installation Procedure Version no. 3
Date: 15/12/06
NF No. Production date Serial No. Personnel: 2
From / / From Time: 20min
To / / To
Note: If the Proteus XR/a collimator is replaced with Eclipse Proteus Collimator unit, remove the lead cup
on tube side before new collimator installation.
Note: For Manual Collimator, the transformer on OTS also needs replaced for proper lamp power supply,
please refer to Job Card IST002 and OTS service manual, after the collimator installation, please refer
to CAL 015 to calibrate lamp voltage.
Note: This Job Card is only for MX100 X-ray tube. For the mounting of Proteus XR/a Collimator to RAD
14,21 X-ray tube, please refer to Job Card IST 014 in this Chapter.

1. Remove the three safety screws with red heads from the
collimator (marked with white ellipses).
Transportation safety screw B

Collimator mounting screws

Transportation safety screw A

2. Check the collimator aluminum plate quantity, if there is only one plate in the collimator-tube interface, please
order one plate 2383309. Make sure there are two plates installed on the collimator-tube interface.
Note: This action in step 2 is only for the MX100 Tube.
For RAD14,21 Tube, only reserve one piece of Aluminium plate.
(Refer to Job Card IST 014)
Aluminium
plate

3. Loosen the three collimator mounting screws to their maximum permissible limit.
Remove all 3 transportation safety screws (marked with white ellipses), see illustration
A and B, before applying power to the collimator.
CAUTION Before transportation tighten the transport safety screws A fully (they have to screw in
easily). Therefore the smallest x-ray field has to be set. For manual setting of the
collimator blades replace the left cover and adjust an opening of the collimator blades
of approx. 4.5 mm.
Turn off voltage before fitting or removing the cover.
Mind installation instructions and ESD regulations.

2-65
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/3 IST 015

4. Rotate the tube 180°.

Note: Step 4 to 5 should be performed only when the
OTS console bracket and collimator interface plate are
not assembled with the MX100 X-ray tube when
arriving at the install site. Otherwise, if the OTS
console bracket and collimator interface plate are
already assembled at the factory, skip to step 6
directly.
5. Mount the OTS console bracket.
Note: Apply locktite to OTS console bracket OTS
mount screws when mounting.
console
bracket
6. Mount the tube/collimator interface plate.
USE SOME MATERIAL TO PROTECT TUBE WINDOW WHEN FASTENING SCREWS.
WARNING PAY ATTENTION TO THE DIRECTION OF PLATE. THE SLOT SHOULD BE ALIGNED WITH
OTS CONSOLE BRACKET.

Apply grease underneath the

tube/collimator interface plate edge
7. Be careful not to damage the collimator fingers. Position the collimator on the X-ray tube. Be sure the detent
lever is not preventing the collimator from seating fully.
The collimator rotation lever must be fully depressed when mounting/installing the
CAUTION collimator to the tube/collimator interface plate. Failure to do so could cause the
collimator to mount improperly and fall from the unit.
Note: Apply grease supplied to collimator mount flange and the tube/collimator interface plate (see picture
below) for easy movement.

Apply grease on
the inside surface
of adapter

2-66
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/3 IST 015

8. Tighten the 3 collimator mounting screws in equal number of turns until they lock securely and can not be
turned anymore. Then back out each screw equally by maximum 1/2 turn, so that collimator can rotate
freely. Verify that when the collimator is not in a detent location, the minimum rotate force is 20N.

9. Turn the X-ray tube back into normal position.

CHECK THAT THE MOUNTING IS CORRECT BEFORE TURNING THE TUBE BACK TO
WARNING NORMAL POSITION.
BE SURE THAT THREE THRUST BUSHINGS ARE SYMMETRIC TO THE CENTER AND HOLD
THE FLANGE FIRMLY.
10. Loosen the X-ray tube. Use level gauge to check that the tube and collimator are in level position, then fasten
the tube using trunion handle securely.

11. Connect the Collimator Power & CAN cable (GPCP No., 2258383).

Note: For MX100 X-ray tube, if the X-ray field and light field of Collimator are not aligned after mounting,
the performing of Job Card IST 032 “MX100 X-ray tube-Collimator Interface Plate Alignment” in
Chapter 3 can calibrate and ensure the alignment of X-ray field and light field of Collimator.

2-67
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 016

Subassembly: Mount Eclipse Proteus Collimator to RAD 14,21 X-ray Tube

Purpose: Installation Procedure Version no. 1
Date: 15/12/06
NF No. Production date Serial No. Personnel:2
From / / From Time: 20min
To / / To
Note: This Job Card is only for RAD 14,21 X-ray tube. For the mounting of Eclipse Proteus Collimator to
MX100 X-ray tube, please refer to Job Card IST 017 in this Chapter.
1. Rotate the tube 180°.

2. Mount the collimator mounting flange and the OTS console bracket with four provided screws.
Note: If the flange has been mounted in the factory, skip this step.
USE SOME MATERIAL TO PROTECT TUBE
WARNING WINDOW WHEN FASTENING SCREWS.
PAY ATTENTION TO THE DIRECTION OF
FLANGE. THE SLOT SHOULD BE ALIGNED
WITH OTS CONSOLE BRACKET.

Note: Apply locktite 242 to flange mount screws.

The force fastening screws is between 10~13 N.m

2-68
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/3 IST 016

3. Loosen the screw (1), put the two clamps outwards to the max opening position. Put the locking Block (3) inside
the holder.
Illustration: Eclipse Proteus Collimator Top View
2
3

4. Position the collimator on the X-ray tube.

Note: Be sure the Locking Block is inside the holder.
Note: Apply grease supplied to collimator mount flange, collimator adapter and locking tongue for easy
movement.

Apply grease Apply grease on

underneath the the inside surface
flange edge of adapter and the
locking tongue
5. Put the two clamps closed. Make sure that collimator is properly connected with the flange.
Note: Tighten the screw (1) in Illustration Eclipse Proteus Collimator Top View with torque of 5.6 Nm.

2-69
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/3 IST 016

6. Loosen the locking screw, rotate the collimator to the normal position,
and then, tighten the locking screw.
Note: The collimator is in normal position only after a click is heard.

7. Turn the X-ray tube back into normal position.

CHECK THAT THE MOUNTING IS CORRECT BEFORE TURNING THE TUBE BACK TO
WARNING
NORMAL POSITION.

8. Loosen the X-ray tube. Use level gauge to check that the tube and collimator are in level position, and then
fasten the tube using trunion handle securely.
Note: For RAD 21 X-ray tube, there is no trunion handle.
Just need to fasten clamp screws.
Apply locktite to mount screws.
9. Mount the OTS Console.
10. Connect the collimator cable (GPCP No., 2258383).

11. Fix the cable on the strain relief screw with M5 nut.
12. Mount the cable cover.

2-70
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 017

Subassembly: Mount Eclipse Proteus Collimator to MX100 X-ray Tube

Purpose: Installation Procedure Version no. 1
Date: 15/12/06
NF No. Production date Serial No. Personnel: 2
From / / From Time: 20min
To / / To
Note: This Job Card is only for MX100 X-ray tube. For the mounting of Eclipse Proteus Collimator to RAD
14,21 X-ray tube, please refer to Job Card IST 016 in this Chapter.
1. Rotate the tube 180°.
Note: Step 4 to 5 should be performed only when the OTS
console bracket and collimator interface plate are not
assembled with the MX100 X-ray tube when arriving
at the install site. Otherwise, if the OTS console
bracket and collimator interface plate are already
assembled at the factory, skip to step 6 directly. OTS
console
bracket
2. Mount the OTS console bracket.
Note: Apply locktite to OTS console bracket mount screws when mounting.
3. Mount the tube/collimator interface plate.
USE SOME MATERIAL TO PROTECT TUBE WINDOW WHEN FASTENING SCREWS.
WARNING PAY ATTENTION TO THE DIRECTION OF PLATE. THE SLOT SHOULD BE ALIGNED WITH
OTS CONSOLE BRACKET.

Apply grease underneath the

tube/collimator interface plate edge

2-71
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/3 IST 017

4. Loosen the screw (1), put the two clamps outwards to the max opening position. Put the locking Block (3)
inside the holder.
Illustration: Eclipse Proteus Collimator Top View 2
3

5. Position the collimator on the X-ray tube.

Note: Be sure the Locking Block is inside the holder.
Note: If the replaced collimator is Siemens unit, remove the lead cup on tube side before new collimator
installation.
Note: Apply grease supplied to collimator mount flange, the tube/collimator interface plate and locking
tongue (see picture below) for easy movement.

Apply grease Apply grease on the

underneath the inside surface of
flange edge adapter and the
locking tongue
6. Put the two clamps closed. Make sure that Eclipse Proteus Collimator is properly connected with the flange.
Note: Tighten the screw (1) in Illustration Eclipse Proteus Collimator Top View with torque of 5.6 Nm.

2-72
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/3 IST 017

7. Loosen the locking screw, rotate the collimator to the normal position,
and then, tighten the locking screw.
Note: The collimator is in normal position only after a click is heard.

8. Turn the X-ray tube back into normal position.

CHECK THAT THE MOUNTING IS CORRECT BEFORE TURNING THE TUBE BACK TO
WARNING NORMAL POSITION.

9. Loosen the X-ray tube. Use level gauge to check that the tube and Eclipse Proteus Collimator are in level
position, then fasten the tube using trunion handle securely.

10. Connect the Collimator Power & CAN cable (GPCP No., 2258383).

11. Fix the cable on the strain relief screw with M5 nut.
12. Mount the cable cover.

Note: For MX100 X-ray tube, if the X-ray field and light field of Eclipse Proteus Collimator are not aligned
after mounting, the performing of Job Card IST 032 “MX100 X-ray tube-Collimator Interface Plate
Alignment” in Chapter 3 can calibrate and ensure the alignment of X-ray field and light field of
Eclipse Proteus Collimator.

2-73
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 1/6 IST 018

Subassembly: Assemble Tube Cover to RAD 14,21 X-ray Tube

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / / From Time: 1 hours
To / / To
Note: This Job Card is only for assembling the tube cover to
RAD 14,21 X-ray tube. For the assembling of the tube
cover to MX100 X-ray tube, please refer to Job Card IST
019 in this Chapter.
1. Mount cable support bracket with two screws.

Note: If Tomo-link function is selected, please use the

bracket marked with “For Tomo”.

2. Insert all cables into cable support.

3.Insert HV cables into HV cable (2269002-3 or 2269002)

socket.
APPLY SILICON GREASE ON BOTH SIDES
WARNING OF PLUGS BEFORE CONNECTING THE
HIGH VOLTAGE PLUG!!

USE HV CABLE WRENCH TO TIGHTEN HV

CABLE SECURELY.

4. Connect stator (2258386 or 2258386-2) and Thermal SW

cables (2258384 or 2258384-2) to X-ray tube. Refer to Job
Card IST 020.

5. Mount cable support onto bracket with two screws.

Hazardous voltage on the Internal Shield of
CAUTION Anode Rotation Cable. It can cause severe
injury, death.Turn off power before any
manipulation of the cable.

2-74
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 2/6 IST 018

6. Connect OTS Console CAN (2259867), OTS Console Lock

PWR (2258381) and Collimator Power & CAN (2258383)
cables. Refer to Jobcard IST 020.Then use ty-rap to fasten
the two cables.

Note: For RAD 21 X-ray tube, these two cables go

through the top of X-ray tube.

Note: Route the Collimator Cable according to the

picture shown here.

Collimator Cable

7. Connect Angulation lock cable. See Illustration.

8. Mount two tube cover adapters to X-ray tube.

Note: This step is for RAD 21 X-ray tube. For RAD 14
X-ray tube, skip to step 9.

2-75
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 3/6 IST 018

9. Mount two tube cover brackets onto X-ray tube.

Note: For RAD 21 X-ray tube, mount the tube cover
brackets onto the adapter.

10. Mount bottom cover under the OTS Console bracket.

Note: For RAD 21 X-ray tube, mount bottom cover onto

the OTS Console bracket.

11. Mount Tube Angulation meter.

Note: For RAD 21 X-ray tube, skip this step.

2-76
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 4/6 IST 018

12. Locate the focal spot label on the tube.

13. Lower the tube and collimator to the table top until the
bottom of the collimator rests on the table top. The bottom
of the collimator should remain flush with the table when the
locks are engaged.
14. Make a reference measurement from the table top to the
center of the focal spot label and record this dimension
(See Figure 1 and Figure 2). It is recommended to use
a steel scale (as shown) with 0.5mm divisions.

15. Mount the front cover.

Note: For RAD 21 X-ray tube, there has no angulation

meter window.

2-77
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 5/6 IST 018

16. Mount two steel straps on both sides of front cover.

Note: For RAD 21 X-ray tube, skip this step.

Steel Strap

17. Adjust the Angulation meter to 0. Then fasten screws.

Note: For RAD 21 X-ray tube, skip this step.

18. Use ty-rap to fasten all cables.

Note: For RAD 21 X-ray tube.

2-78
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 6/6 IST 018

19. Mount both side covers and fasten screws.

If screw holes don’t match, loosen the four screws in side

cover a little.

Re-adjust the bracket position. Then mount the side cover.

20. Using same gage as in step 3 to determine the location of

the focal spot label on the tube cover, roughly in the center
of the cover in the system Lateral direction.

21. Apply the focal spot label (46-239720P2) such that the
center of the focal spot label coincides with
the dimension recorded in step 13.

2-79
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 1/7 IST 019

Subassembly: Assemble Tube Cover to MX100 X-ray Tube

Purpose: Installation Procedure Version no. 0
Date: 03/01/03
NF No. Production date Serial No. Personnel: 1
From / / From Time: 1 hours
To / / To
Note: This Job Card is only for assembling the tube cover to MX100 X-ray tube. For the assembling of
the tube cover to RAD 14,21 X-ray tube, please refer to Job Card IST 018 in this Chapter.
1. Mount cable bracket (GPCP No. 2365447) with two
screws.

2. Insert all cables into cable support.

3. Insert HV cables into HV cable (2269002-3 or 2269002)

socket.
Apply silicon grease on both sides of
WARNING plugs before connecting the High Voltage
plug!!
Use HV cable wrench to tighten HV cable
securely.
4. Connect Rotation cable (2380062 or 2380062-2), Thermal
SW cable (2380063 or 2380063-2) , and other tube cables
to X-ray tube. Refer to Job Card IST 020.

Tube
fan
cover

2-80
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 2/7 IST 019

5. Secure cables to cable entrance cover with clamp.
Note: Because of the size of cables is larger than the clamp,
you can use the clamp to secure the single largest
cable only. And make other cables accompany with
the clamped cable when exiting from the hole on the
cable entrance cover.

6. Mount cable support onto bracket with two screws.

Hazardous voltage on the Internal Shield of

CAUTION Anode Rotation Cable. It can cause severe
injury, death.Turn off power before any
manipulation of the cable.

7. Mount the OTS console.

space

8. Connect OTS Console CAN (2378473), OTS Console Lock PWR (2378475) to the back of OTS Console.

2-81
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 3/7 IST 019

9. Connect Angulation lock cable. See Illustration.

10. Locate the focal spot label on the X-ray tube.
11. Lower the tube and collimator until the bottom of the
collimator rests on the table top and engage the vertical lock.
12. Using a steel scale, measure and record the distance from
the table top to the focal spot.

Note: Refer to Illustration “LOWER TUBE COVER INSTALLATION” on the next page while performing
the following steps.
13. Install the end cover mounting brackets (1&2) on both ends of the tube using three (3) screws for each bracket.
14. Install the bottom cover (4) using 2 screws and washers (5).

2-82
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 4/7 IST 019

LOWER TUBE COVER INSTALLATION

15. Install the tube indicator.

1) Connect the tube indicator with tube indicator cable (indicator end: 2318489), and put the pin on.

Frontal of Rear of
indicator indicator

2-83
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 5/7 IST 019

pin

2) Insert the two pins (indicator end and tube end).

Insert

16. Install one screw on each side of top cover. Engage each screw only a few turns to allow the tab on bottom
cover to slide under the screw head.

2-84
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 6/7 IST 019

17. Install the top cover (6) and secure using 2 screws (7) on the upper back.

18. Squeeze the top and bottom cover together and tighten the two screws (8) that were started in step 16. When
complete, the cover gap should look like Illustration below.

19. Install 2 end cover mounting screws (9) in each end cover mounting bracket. One from the bottom and one
from the back. Engage each screw only a few turns leaving room for the end cover internal bracket to slide
between the screw head and the end cover mounting bracket (1&2).

20. Position the end covers (10&11) by sliding the slots on the internal bracket under the screw heads on the end
cover mounting brackets.

21. Tighten the four screws (9) that were only started in step 17. The bottom screw is accessed through a hole in
the end cover.

22. Secure the end covers (10&11) by installing two screws (12&13) through each end cap and into the top cover.

2-85
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 7/7 IST 019

23. If necessary, adjust the counterpoise spring to eliminate any vertical drift of the OTS.

24. Using the same metal scale and the dimension recorded earlier, determine the location of the focal spot and
apply the new focal spot decal in the center of the anode X-ray tube cover.

2-86
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 1/12 IST 020

Subassembly: Electrical Connections

Purpose: Installation Procedure Version no. 1
Date: 12/12/05
NF No. Production date Serial No. Personnel: 1
From / / From Time: 1and half hours
To / / To

THE PDU CONTAINS TWO POWER TRANSFORMERS. THE FACTORY DEFAULT INPUT
WARNING IS SET TO 380V. THE FIELD ENGINEER MUST ADJUST INPUT VOLTAGE ACCORDING
TO LOCAL POWER.

The transformer schematics are shown as follows.

Jumper VB
Jumper VA

Default Factory Setting

1. Adjust the jumper VB and jumper VA according to local power voltage.

2. Connect all cables according to following table.
3. Apply silicon grease on both sides of plugs before connecting the High Voltage plug!!
4. Pay attention to the polarity of the X-ray tube. Incorrect connection will destroy the X-ray
tube.
5. Connect system power cable.

ALL COMPONENTS MUST BE SECURELY GROUNDED.

WARNING
MAKE SURE THAT PLUGS ARE NOT LOOSE!
CHECK WHETHER ALL CABLES ARE CONNECTED CORRECTLY.
THE EXCESS SHOULD BE PUT IN PROPER PLACE. IF NEEDED,
COIL THE EXCESS CABLE. FOR SAFETY AND MAINTENANCE, ALL
CABLES SHOULD BE WRAPPED AND FIXED.

6. After checking components grounding and cable connections, power on the system.

2-87
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 2/12 IST 020

Item Cable Name Cable Parts Supplier Plug or Connector Fini
Num- Number Number sh
ber One End The Other End
1 OTS power cable (2m) 2258387 OTS J100 PDU CN19
1-1 OTS power cable (3m) 2258387-2 OTS J100 PDU CN19
2 OTS Grounding Cable 46-315243G3 OTS PDU GND
3 OTS SID & tomo I/O Cable (2m) 2258388 OTS J101 Connector 3 (on the
top of OTS)
I/F Board J111
3-1 OTS SID & tomo I/O Cable (3m) 2258388-2 OTS J101 Connector 3 (on the
top of OTS)
I/F Board J111
4 *2 OTS CAN Cable (2m) 2258389 OTS CN3 I/F Board J116
4-1 OTS CAN Cable (3m) 2258389-2 OTS CN3 I/F Board J116
*2
5 Rotor control Cable (2m) 2258386 Jedi Tube
5-1 Rotor control Cable (3m) 2258386-2 Jedi Tube
5-2 Rotor control Cable (2m) for MX100 2380062 Jedi Tube
5-3 Rotor control Cable (3m) for MX100 2380062-2 Jedi Tube
6 Thermal SW Cable (2m) 2258384 Jedi Tube
6-1 Thermal SW Cable (3m) 2258384-2 Jedi Tube
6-2 Thermal SW Cable (2m) for MX100 2380063 Jedi Tube
6-3 Thermal SW Cable (3m) for MX100 2380063-2 Jedi Tube
7 HV Cable (20m) 2269002-3 Tube Jedi
7-1 HV Cable (24m) 2269002 Tube Jedi
8 *2 Collimator power & CAN Cable 2258383 OTS CN1 Proteus XR/a
Collimator/Eclipse
Proteus Collimator
9 *2 OTS Console Power & CAN Cable 2259867 OTS CN4 OTS console
9-1 OTS Console Power & CAN Cable 2378473 OTS CN4 OTS console
for MX100 tube
10 *1 OTS Console Locks Power Cable 2258381 OTS power board OTS console
Lower connector
10-1 OTS Console Locks Power Cable 2378475 OTS power board OTS console
for MX100 Lower connector
11 OTS Long SID Switch Cable (2m) 46-329249G3
11-1 OTS Long SID Switch Cable (3m) 46-329249G4
12 Ground Lead 15.5 Foot 46-216211G16
13 OTS I/F PCB To PWR Supply Cable 2268131 OTS power board OTS J1
Higher connector
14 OTS Angulation Lock Cable 46-329256G3
15 Table height sensing Cable 2259298-56 221-2726 I/F Board J110 Table
16 AEC(1) Jedi AEC1 Ion chamber
17 Table cassette size sensing Cable
2259298-58 221-2727 I/F Board J112 Cassette tray
18 Table bucky control Cable 2259298-63 M720092- Jedi Table bucky Bucky
1
19 Table power Cable 2259298-57 221-2725 PDU CN20 Table
20 Table grounding Cable 2259298-66 221-2738 PDU GND Table
21 AEC(2) Jedi AEC2 Ion chamber
22 Wall Stand (GPCP No. 2260354) 2259298-58 221-2727 I/F Board J113 Bucky
cassette size sensing Cable
23 Wall Stand (GPCP No. 2260354) 2259298-63 M720092- Jedi Wall bucky Bucky
bucky control Cable 2

2-88
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 3/12 IST 020

24 Wall Stand (GPCP No. 2260354) 2259298-65 600-3025 PDU CN17 Wall Stand
power Cable
25 Wall Stand (GPCP No. 2260354) 2259298-73 221-2738 PDU GND Wall Stand
grounding Cable
26 SG100 Wall Stand (GPCP No. 2145644-2 System I/F Board SG100 Wall
2225849) Auto Tray Cable connector J124 Stand
27 SG100 Wall Stand (GPCP No. 2145641-2 Jedi Wall Bucky (J6) SG100 Wall
2225849) Bucky Cable connector Stand
28 SG100 Wall Stand (GPCP No. 2140362-2 PDU GND SG100 Wall
2225849) Ground Cable Stand
29 SG100 Wall Stand (GPCP No. 2145642-2 Jedi AEC2 SG100 Wall
2225849) Ion Chamber Cable Stand
30 SG100 (GPCP No. 2225849) Power 2151729-2 PDU connector TM4 SG100 Wall
Supply Cable SG100 Power Stand
Note: On PDU end of the SG100 Power
Supply cable, connect the wire
marked “10” to the connector
marked “1” of TM4 SG100 Power,
connect the wire “11” to connector
“2”, connect the yellow-green wire
to connector in yellow-green color.
31 SG120 Wall Stand (GPCP No. 2145644-2 System I/F Board SG120 Wall
2402562) Auto Tray Cable connector J124 Stand
32 SG120 Wall Stand (GPCP No. 2145641-2 Jedi Wall Bucky (J6) SG120 Wall
2402562) Bucky Cable connector Stand
33 SG120 Wall Stand (GPCP No. 2140362-2 PDU GND SG120 Wall
2402562) Ground Cable Stand
34 SG120 Wall Stand (GPCP No. 2145642-2 Jedi AEC2 SG120 Wall
2402562) Ion Chamber Cable Stand
35 SG120 (GPCP No. 2402562) Power 2410108-2 PDU connector TM4 SG120 Wall
Supply Cable SG120 Power Stand
Note: On PDU end of the SG120 Power
Supply cable, connect the wire marked
“10” to the connector marked “1” of TM4
SG100 Power, connect the wire “11” to
connector “2”, connect the yellow-green
wire to connector in yellow-green color.

2-89
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 4/12 IST 020

36 Tube fan power cable (from tube fan 2365706 PDU connector CN21 Tube terminal
to cabinet) for RAD21 tube Tube fan power strip
Note: Pay attention to ensure the
grounding of the Tube fan power
cable with the P-clamp on cabinet.
Use the same one P-clamp to
ground the Wall Stand power cable
(Item Number 24 in this table)
together with the Tube fan power
cable if the Wall Stand (GPCP No.
2260354), not SG100 Wall Stand, is
selected.

P-clamp for Tube fan power

cable grounding.
37-1 Tube fan power cable for MX100 2378816 PDU connector CN21 Tube terminal
tube Tube fan power strip
37-2 Tube fan power cable for MX100 2378816-2 PDU connector CN21 Tube terminal
tube Tube fan power strip
38 System Console Signal Cable 2259298-60 2259977 I/F Board J119 Console
39 PDU power Cable BK(LU, LV, LW) 3 phase power
40 PDU grounding Cable PDU GND Power GND

2-90
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 5/12 IST 020

PDU HAS 380-480V POWER EVEN WHEN THE CONSOLE TURNED OFF BUT CIRCUIT
WARNING BREAKER ON.

Note: To install OTS SID cable, unplug the

old cable from connector 3 on the
top of OTS, then plug in the new
SID cable come from OTS J101.

Note: The following pictures show cable

connector location.
Refer to OTS service manual for
detailed OTS schematics.
*1: *2:

Note: If use manual collimator, FE needs

to connect Collimator power & CAN
Cable to Manual Port (CN2), at the
same time, plug the CAN signal
terminal to Auto Port (CN1). Collimator Cable

CAN signal Terminal

2-91
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 6/12 IST 020

Note: Use P-clamps to hold the shield

piece of AEC cable and fasten the
two P-clamps on the bottom of the
cabinet.

ANODE ROTATION STARTUP CABLE CONNECTION

Note: Grounding wire must be connected properly.
VARIAN X-RAY TUBE RAD-12, 14 KOUSHAL X-RAY TUBE MX100
Anode rotation cable and Tube anode terminals Connect point Anode rotation Tube
Thermal Protection cable (count from cable and Thermal terminals
the right side Protection cable
when facing
the OTS)
C 5 1 Black (M) Black
M 4 2 Green (A) Green
A 3 3 White (C) White
SW 1 4 TB1-4 (Black) Brown, Black
(group from
pilot light),
Black (group
outing from
the front hole)
SW 2 5 TB1-5 (White) Five, Black
(group from
pilot light),
Black
Rotation Cable outer Housing Clamp 6 - Six, Black
Shield (group outing
from the front
hole), Black
Thermal Protection Housing Clamp 7 THR2 Red
Cable Shield
E Housing Ground 8 THR1 Black

2-92
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 7/12 IST 020

VARIAN X-RAY TUBE RAD-21

Anode rotation cable and Tube anode terminals
Thermal Protection cable
White ( C ) White
Black ( M ) Black
Green ( A ) Red
SW Brown
SW Brown-Orange
Rotation Cable outer Housing Clamp
Shield
Thermal Protection Housing Clamp
Cable Shield
E Housing Ground

DC BUS (+) IS ACTING AS INNER

WARNING SHIELD, WHICH IS PROTECTED BY
HEAT SHRINK TUBE. DON'T
SHORTEN THE LENGTH OF
ROTATION CABLE. MAKE SURE ALL
THE CONNECTIONS AT TUBE HEAD
ARE FASTENED ENOUGH TO
SEPARATE THE INNER SHIELD AND
GROUNDING.

Note: For MX100 X-ray tube, pay attention to ground the tube grounding cable (Green-Yellow
group) and tube fan shield grounding cable (labeled with “F3”) to the tube casing. Refer to
the illustration on prior page.

Note: For Rad 14,21 X-ray tube, to avoid possible slipping, clamps must not be put over the plastic
labels wrapped around the end of the stator cable. Remove the plastic labels when
necessary. (See figures below)

Note: For Rad 14,21 X-ray tube, when replacing the old tube with new one, the stator cable strain
relief parts and Cable clamps used to fix the cables should be retained and re-installed to
the new X-ray tube. (See figures below)

Figure 1: RAD 14 X-ray Tube Figure 2: RAD 21 X-ray Tube 3x M4

Cable strap
Cable Clamp screws.

1xM4 screw,
2xM4 flat washers.
Thermal cable Apply Loctite
242(46-170686P1)

clamp
mounting
block
Stator cable
Attach P-clamp Copper
using M4 hex. nut strap
2-93
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 8/12 IST 020

ANODE ROTATION STARTUP CABLE CONNECTION

Note: Grounding wire must be connected properly.
Jedi Generator Side
Anode rotation cable and Thermal Protection cable Jedi Generator Connector
2 J3 (2)
1 J3 (1)
3 J3 (3)
15 J2 (15)
16 J2 (16)
Rotation Cable outer Shield E2
Thermal Protection Cable Shield E1

Rotation Cable inner Shield J3 (4) DC BUS plus (+)

Note: Please use the P-clamp (on the top of Jedi) to grounding the shield layer of the tube rotor
cable and thermal cable.
Make sure that cables should be placed at inner sides of the P-clamps, or else it will be
difficult to fasten the bolts.
Make sure the P-clamps are tight enough so that they can contact with cable shield well.

Heat protection Anode rotation

cable start up cable

16 15

5 4 3 2 1
Bus DC A C M
- +

Note: Make sure the brown wire from inner shield is connected to J3 (4) DC BUS (+)"

2-94
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 9/12 IST 020

BUCKY CABLE CONNECTION

Table
Bucky (J5)
PIN1

Wall Bucky (J6)

(also for SG100
PIN1 or SG120)
SAFETY DOOR AND LIGHT SWITCH
For connecting the Safety Door and Light Switch, see
Safety Door
page 10-26, 59. Connect the connector J7 to door light
and Light
circuit.
Switch (J7)
Maximum Ratings for Door Light Power: 250V/2A PIN1

Service
We suggest to use the shield Terminal (J8)
NOTICE
cables as the Safety Door and
Light Switch cables, and their
shield layer should grounded Inside Comm-
to the system ground. unication (J9)

AEC CABLES CONNECTION

AEC1
• AEC1: Table Ion Chamber

• AEC2: Wall Stand (GPCP No. 2260354) Ion Chamber AEC2

(or SG100 Wall Stand (GPCP No. 2225849) Ion Chamber

or SG120 Wall Stand (GPCP No. 2402562) Ion Chamber)

2-95
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 10/12 IST 020

CABLE HOSES CONNECTION

1. Use ty-rap to attach the cable and hose to the telescopic
column.

2. Put excess cables back into cable hose.

Cable hose

3. Hang the cable hose along stationary rail and make sure
OTS bridge can move freely.

4.Put the excess cables into floor duct or ceiling.

2-96
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 11/12 IST 020

PRINTER CABLES CONNECTION (UPGRADE)

1. Unplug the connector on the socket J120 on the I/F board, plug the connector of the cable 221-2872.

Cable 221-2872

2. Unplug the connector on the socket J15 of the PDU, plug the other connector of the cable 221-2872.

3. Connect the cable 221-2872 with the cable 221-2871. Cable 221-2872
Connect the cable 221-2871 with the printer.

Cable 221-2871 Cable 221-2872 Cable 221-2871

2-97
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 12/12 IST 020

SYSTEM I/F BOARD (GPCP NO. 2375230) ELECTRICAL CONNECTION

Connector # 1
Connector # 9
Connector # 2
Connector # 10
Connector # 3, 4

Connector # 5 Connector # 11
Connector # 6
Connector # 12

Connector # 7
Connector # 13

Connector # 8 Connector # 14

Connector # Cable Name GPCP No. Connector Mark Other end

System I/F Power 221-2886 J114 PDU CN16
1
Cable
Wall Stand (GPCP No. 2259298-58 J113 Wall Stand
2 2260354) cassette size
sensing Cable
SG100 Wall Stand 2145644-2 J124 SG100 Wall
3 (GPCP No. 2225849) Stand
Auto Tray Cable
SG120 Wall Stand 2145644-2 J124 SG120 Wall
4 (GPCP No. 2402562) Stand
Auto Tray Cable
Table cassette size 2259298-58 J112 Table Cassette
5
sensing Cable Tray
Table height sensing 2259298-56 J110 Table
6
Cable
OTS SID & TOMO I/O 2258388/2258388-2 J111 OTS J101
7
Cable (2m/3m)
8 (optional) J123 (CAN port)
OTS CAN Cable 2258389/2258389-2 J116 XT CN3
9
(2m/3m)
System I/F Board 221-2893 J120 PDU CN15
10 J120-PDU CN15
Cable
System Console Signal 2259298-60 J119 System
11 -Power Cable (Supplier Console
No. :2259977)
System I/F Board – 221-2888 J118 Jedi CAN
12
Jedi CAN Cable
System I/F 221-2734 J115 Tomo I/F Board
13
Board-TOMO Cable P2
System I/F Board – 221-2887 J117 Jedi I/F J1
14
Jedi Signal Cable

2-98
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 021

Subassembly: Align Table Bucky with Proteus XR/a Collimator / Eclipse Proteus Collimator
Purpose: Installation Procedure Version no. 0
Date: 20/12/1999
NF No. Production date Serial No. Personnel: 1
From / From Time: 1h
/ To
To /
/
Table Bucky and Proteus XR/a Collimator/Eclipse Proteus Collimator Alignment
Note: The front panel of the wall stand is removable, so before this step, perform wall stand
panel alignment calibration first.
Note: The following procedures for Table Bucky/Collimator Alignment may require slight
repositioning of the table base. This movement may affect the position or arrangement of
the levelling plates, requiring an additional check prior to the final table mounting.
Note: Collimator calibration, OTS/collimator alignments and collimator light field to x-ray field
adjustments, as described in their respective manuals, must be performed prior to the
following procedure.
MAKE SURE ALL CABLE CONNECTIONS ARE CORRECT AND ALL GROUND WIRES
WARNING ARE FASTENED. DAMAGE TO EQUIPMENT COULD OCCUR IF COMPONENTS ARE
NOT PROPERLY SET BEFORE INITIAL UP.
1. If the table top is installed, remove the table top (keep
table top frame on) by removing the two screws at each
end of the table top underside. Then take the table top
out of the frame.

2. With the collimator parallel to the table top, turn on the

collimator light, and using the light field adjusting knobs
on the collimator, reduce the light field to a narrow beam Proteus XR/a Collimator/Eclipse Collimator Light
of light along the length of the table.

3. Position the collimator to approximately 24"

SID. (Source-to-Image- Distance).

4. Move the entire table so that the longitudinal center of

field beam is properly aligned with the two center marks Light field Knob
on the bucky.

5. Move the OTS and bucky simultaneously to check for

continuous alignment of the narrow beam of light to the
center marks.

Note: Since the bucky has previously been “squared” to the bucky rails, any deviation from
alignment may be due to inaccurate alignment of either the OTS or collimator. If necessary,
repeat alignment procedures.
Note: Light field to x-ray field alignment should be performed before this step.

2-99
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 022

Subassembly: Align Wall Bucky with Proteus XR/a Collimator (for Wall Stand (GPCP No. 2260354) and
SG100 Wall Stand (GPCP No. 2225849)), Eclipse Proteus Collimator (for SG120 Wall
Stand (GPCP No. 2402562))
Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / From Time: 30 min
/ To
To /
/
Note: Proteus XR/a Collimator, Eclipse Proteus Collimator, SG100 Wall stand and SG120 Wall
Stand should follow the below contents.

Wall Bucky and Proteus XR/a Collimator/Eclipse Proteus Collimator Alignment

Note: The following procedures for Wall Bucky/Collimator Alignment may require slight
repositioning of the wall stand. This movement may affect the position or arrangement of
the levelling plates, requiring an additional check prior to the final wall stand mounting.
Collimator calibration, OTS/collimator alignments and collimator light field to x-ray field
adjustments, as described in their respective manuals, must be performed prior to the
following procedure.

Note: For SG100 and SG120 Wall Stand, ensure the Bucky to be in vertical position before
performing the following steps.

1. Rotate the collimator towards wall bucky by pressing

Ang. key on the OTS console.

2. With the collimator parallel to the wall bucky panel, turn

on the collimator light and, using the light field adjusting
knobs on the collimator, reduce the light field to a narrow
beam of light along the length of the table.

3. Position the collimator to approximately 40" SID.

(Source-to-Image-Distance).
Beam of
light
4. Move and shim the wall stand so that the vertical
centerline on the panel is properly aligned with the
narrow beam of light.

5. Move the OTS to approximately 72" SID to check for

continuous alignment of the narrow beam of light to the
panel centerline.

Note: Light field to x-ray field alignment should be performed before this step.

2-100
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 023

Subassembly: Mount Anchor bolts

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / From Time: 20 min
/ To
To /
/
AVOID POSSIBLE SEVERE INJURY!
TO PREVENT POSSIBLE SEVERE INJURY, AT LEAST TWO PEOPLE ARE
WARNING
REQUIRED TO MOVE THE TABLE OR WALL STAND.

1. Remove four table upper covers, from table

base. If needed, remove lower covers too.

2. Drill four anchor holes for fasten table base.

Mount expanding bolts in the table-base anchor
holes. Use expanding bolts supplied in shipping Anchor
bag. holes

3. Leave the bolts loose for levelling and shimming later.

4. Level the table base and shim as necessary with provided shims. If possible place shims close to the
anchor bolts. Check longitudinal and transversal levelling with an extended level (such as a 3-foot or
1meter level) placed over table top.
Note: If shims added, be sure to add shims to foot pedal also.
Note: For SG100 Wall Stand, please skip to step 11 for the Anchor bolt mounting.
Note: For SG120 Wall Stand, please skip to step 17 for the Anchor bolt mounting.
5. Level the wall Bucky and shim as necessary with provided shims. After the table base levelling is
verified, fasten the anchor bolts, then re-check levelling again and make final adjustments.

6. Fasten the wall stand to wall by supplied bracket. Refer to page

4-4 in Proteus XR/a Pre-installation manual for wall mount
dimension.
7. Open the back cover of the wall stand.

2-101
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 2/3 IST 023

8. Insert the cassette tray

9. Balance the counter weight of the cabinet
10. Assemble the back cover.

Note: For SG 100 Wall Stand, the Anchor bolt mounting should follow the steps from 11 to 16,
instead of step 5 to 10.

Note: The procedures in following steps are concerted with the revision 6 of SG 100 Wall Stand
Service Manual. For the reason of the update and change in that manual, it is
recommended to see also the latest Service Manual of SG 100 Wall Stand for reference.
11. Using two people, carefully raise the SG 100 to an upright position.
12. Stand the SG100 against the wall and attach to the wall using the locally provided (6) wall anchors.
13. Align the SG100 laterally across the wall, to the X-Ray Tube Suspension beam or table centerline
using the centerline marks on the wall and floor or the Laser Alignment Tool.
Note: The SG100 must be level on the wall with no more than 1/16 in. (1.5 mm) deflection to
ensure that the anchors holding the SG100 to the wall does not come loose over time.
Use the shims provided with the SG100 to ensure this requirement.
14. Verify the SG100 level across wall to ensure that no more than 1/16 in.(1.5mm) deflection exists,
laterally or vertically. See following Illustration for recommended placement of the levels.
15. Insert supplied shims, as required, between the SG100 and the wall.
16. Tighten the six SG100 anchor bolts according to the torque specifications for the anchors.

2-102
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 3/3 IST 023

Note: For SG120 Wall Stand, the Anchor bolt mounting should follow the steps from 17 to 23,
instead of step 5 to 10.

Note: The procedures in following steps are concerted with SG120 Wall Stand Service Manual
(P/N: S0012532). For the reason of the update and change in that manual, it is
recommended to see also the latest Service Manual of SG120 Wall Stand for reference.

17. Place SG120 at the distance focal dependant to the anti-diffusion grid.
18. Align SG120 laterally using the collimator light or the laser alignment tool.
19. Using the base template of SG120, mark the holes.

20. Move SG120 and drill the holes. Place the anchors.
21. Replace SG120 and place the anchor bolts.
22. Level the equipment using the 3 levelling screws and tight the bolts.

Levelling screws

23. Recheck the alignment of SG120.

2-103
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/1 IST 024

Subassembly: Tomo-Link Assembly

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel:1
From / / From Time: 3 hours
To / / To

Note: For Tomo-Link installed with the system, refer to Job card IST 025 “Tomo-Link
installation” in Chaper3.

Step 4 to 8 are for Tomo-link updating procedure.

2-104
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/7 IST 025

Subassembly: Installation Check

Purpose: Installation Procedure Version no. 0
Date: 20/12/99
NF No. Production date Serial No. Personnel: 1
From / / From Time: 40 min
To / / To

1. If table top was already installed, remove it first.

2. Mount the table lower covers, and then mount
upper covers on.
Note: Lower side cover mount screws are OTS
attached to the table bottom plate. Cover

Note: When mounting right and left upper

side cover, loosen the mount screws,
then insert the side cover along the
mount slot.

Upper
Cover Lower
Cover

Note: Adjust the upper covers’ position to make

sure upper covers will not scratch with
lower covers when elevating the table.
Then tighten all screws.
3. Mount the table top and fasten the four screws
under the table top.
Console
4. Mount OTS carriage cover. label
5. Clean table, console, wall stand (GPCP No.: 2260354) (or SG100 Wall Stand (GPCP No.: 2225849), or
SG120 Wall Stand (GPCP No.: 2402562)) and OTS suspension surfaces.

2-105
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 2/7 IST 025

6. Paste the console label provided with the equipment according to local regulation.

Note: After completing installation, remove vinyl protective films from table top and
pedals.
7. Abdomen Compression Band Installation

Adapting screw

Safety

Lock Lock

Depress the lock, then release clamp.

Position the clamp, then depress the handle.
Fasten the compression band.

8. Patient Hand Grips

The patient hand grip installation is as same as compression band clamp.

Lock

2-106
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 3/7 IST 025

9. Adjusting

Depress the lock, then release clamp or grip.

Position the clamp or grip, then depress the
handle.
Release two safety screws.
Use M2.5 allen key adjust two adapting
screws until clamp is firmly attached to table
top
Fasten safety screws. Safety screw

Adapting
screw
10. Collimator Cone
Note: The following contents fit to both Proteus XR/a Collimator and Eclipse Proteus Collimator.
Note: The purpose of the collimator cone is to collimate the beam and image to a cylinder shape
when doing certain procedures. Mainly used for sinuses, head, hip etc.

Procedure of attach and removal:

I. Insert the edge of the collimator cone into the Accessory Rails beside the collimator window.

CAUTION Insert collimator cone into the upper accessory rail.

Note: Adjust the alignment of the collimator cone with the collimator to ensure the concentricity of
the collimator cone and collimator window.

When taking exposure using the collimator cone, pay attention to choose correct
CAUTION cassette size to avoid the X-ray field to beyond the film size.

Accessory Rail

2-107
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 4/7 IST 025

Collimator Cone

Proteus XR/a Collimator Eclipse Proteus Collimator

ii. For removal, push in the Accessory Locking Spring and remove the collimator cone.

Accessory
Locking Spring

For Proteus XR/a Collimator For Eclipse Proteus Collimator

Note: If choose SG120 Wall Stand, please refer to the following contents.

11. Patient Support

Installation
Tools required:
- Standard service person tool kit.
Procedure
1) Do not discard any packing material such as envelopes, boxes, bags until all parts are compared
against the packing list.
2) Check the general condition and external appearance of all parts for possible damage or missing
items. Notify the distribution center immediately of any damage or missing parts.

2-108
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 5/7 IST 025

3) Remove the back covers of the bucky support assembly.

4) Install patient handgrips.

Assembly with the supplied screws in the kit the 2 hand grips (one on each side) in the holes marked
in the figure below.

5) Install lateral bar.

a. Assembly the sheet metal support to the bucky support assembly (6 screws).
Sheet Metal Support

2-109
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 6/7 IST 025

b. Assembly the slide track to the sheet metal support.

c. Take the lateral bar steel weldment assembly and the Teflon strip that is supplied with the
kit and apply it with adhesive along the contact surface between the steel weldment
assembly and the slide track.

d. Fit the steel weldment assembly to the slide track and make sure it can be displaced along
the whole track.

2-110
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 7/7 IST 025

e. Assembly the two magnets (one on each side) included in the kit to the bucky support. The
magnets will lock the inertial sliding movement when the bucky assembly is rotated, in the
case of SG120.

f. Put the lower back cover removed in step 3).

g. Assembly the upper back cover included in the kit.
h. Fit the lateral bar assembly in the steel weldment assembly on the left of the figure below.

i. To remove the lateral bar, press the key on the lateral bar assembly and extract it by pulling
up on the right of the figure above.

6) Add the needed counterweight included in the kit and proceed to counterbalance the bucky and bucky
carriage as described in step 5 in Jobcard IST 009.

2-111
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A 1/3 IST 033

Subassembly: Spanish Language Labels

Purpose: System Installation Version no. 0
Date: 02/06/03
NF No. Production date Serial No. Personnel: 1
From / / From Time: 10minutes
To / / To
Note: For Systems installed at Spain, the Spanish language labels must be applied on
sites to cover the English description area on the English labels attached at the
factory.
1. Pick up the plastic package marked “2382506” from Accessories crate #4, box 4-6.
2. Attach the Spanish labels to cover the description area of the English labels on the subassemblies according
to the forms below.
Form1 Spanish Label Package (Part No. 2382506) Contents
Note: For backup, the quantity of the labels is more than the least number needed to be
applied.
Item Label Part Quantity Applied Subassembly
# Number
1 2382338 9 Table
Wall Stand (GPCP No. 2260354)
OTS
Cabinet
System Console
2 2382341 2 Proteus XR/a Auto Collimator
3 5116700 9 Eclipse Proteus Collimator
4 2382340 2 X-ray Tube (RAD-14/21)
5 2384005 2 X-ray Tube (MX 100)
6 2384006 2 SG100 Wall Stand （GPCP No. 2225849）

Form2 Spanish Label Designation

DESIGNATION System console Wall Stand SG 100 Wall Stand
(GPCP No. 2260354） （GPCP No. 2225849）
SPANISH LANGUAGE 2382338 2382338 2384006
LABELS PART NO.
LOCATION OF NAME PLATE

LOCATION OF SPAIN
LANGUAGE LABELS

2-112
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 2/3 IST 033

DESIGNATION Cabinet OTS radiographic Proteus XR/a Auto

suspension(2/3m) Collimator
SPANISH 2382338 2382338 2382341
LANGUAGE LABELS
PART NO
LOCATION OF NAME
PLATE

LOCATION OF SPAIN
LANGUAGE LABELS

DESIGNATION X-ray Tube (RAD-14/21) X-ray Tube (MX 100) Table

SPANISH 2382340 2384005 2382338
LANGUAGE LABELS
PART NO
LOCATION OF NAME
PLATE

LOCATION OF SPAIN
LANGUAGE LABELS

2-113
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/A SYSTEM 3/3 IST 033

DESIGNATION
Eclipse Proteus Collimator
SPANISH 5116700
LANGUAGE LABELS
PART NO
LOCATION OF NAME
PLATE

LOCATION OF SPAIN
LANGUAGE LABELS

2-114
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 3 SYSTEM UPGRADE OR REPLACEMENT

SECTION 1 TABLE OF JOBCARDS CONTENTS

Jobcard Number Content Version Page

SW JEDI 41-3 AEC Board Option Installation 0 3-3
PROTEUS XR/A Replacing the collimator D1 board, D2 board, Fuse, 1 3-6
COLLIMATOR Tape Measure
ECLIPSE PROTEUS Replace the whole collimator, collimator control board, 1 3-12
COLLIMATOR user interface board, bucky centering light, LCD display,
tape
Table Logical Board or Table Motor Replacement 3 3-19
IST 023 Bucky Installation 0 3-29
IST 024 Ion Chamber Installation 0 3-30
IST 025 Tomo-Link Installation 1 3-32
IST 026 Proteus XR/a Collimator bulb, Fan replacement 0 3-39
IST 027 APR Floppy disk recovery 0 3-41
IST 028 OTS Console Replacement 0 3-42
IST 029 System Console Replacement 2 3-43
IST 030 Proteus XR/a Collimator Eprom update 0 3-44
IST 031 KV Control Board replacement 0 3-49
IST 032 MX100 X-ray tube-Collimator Interface Plate Alignment 0 3-50

3-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

3-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2 JOBCARDS CONTENTS

PROTEUS XR/a 1/3 SW JEDI 41-3

subassembly: AEC BOARD OPTION INSTALLATION

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 20 min
to / / to

1 SUPPLIES

The following items are supplied:

• AEC board
• 1 flat cable
• 6 screws

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, be sure to wear the antistatic bracelet.

4 PREREQUISITES

None.

3-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 SW JEDI 41-3

5 AEC BOARD INSTALLATION

The installation of the AEC Board can

NOTICE
be done without removing the
Interface Unit from the Cabinet.

Interface Unit

1. Unscrew twelve 5.5 mm screws that retain

1 the cover panel and remove the cover 1 .

2. Mount the AEC board to the plate with six

screws

3. Connect the flat cable to connector J5 on the

AEC board and to J3 on the I/F RAD Board.

4. Join connector J1 on AEC board to AEC 2 on

the left side of this module.

5. Join connector J2 on AEC board to AEC1 on

the left side of this module.

3-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 SW JEDI 41-3

6. Join connector P230 come from wiring harness J1 to

TP1 on AEC board

7. Join connector P230 come from wiring harness J2 to

TP2 on AEC board

8. Remember to connect cable from ionization chambers to AEC1 and AEC 2.

AEC board

J5

J1
J2
Rad I/F board

TP1

TP2

6 REASSEMBLY
Remount the Front cover. Reverse the disassembly procedure.

3-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/6 PROTEUS XR/A

COLLIMATOR

subassembly: Replacing the collimator D1 board, D2 board, Fuse, Tape Measure

purpose: version no. 1
date: 31/08/01
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

1 THE D1 OR D2 DOARD ABNORMAL INDICATIONS

The Proteus automatic collimator AL01F is equipped with 2 electronic boards D1 and D2. In general,
- D1 board contains the CAN controller SW
- D2 board contains the lamp regulation system and is also dedicated to the user interface (digital display on the
collimator front panel)

Indications of a defect inside D1 board:

· LED V3 (red, mistake) constantly ON.
· LED V6 (green, CAN 5V supply) does not shine, although CAN power supply of 12 V is recognized in D1, plug
X3 exists.
· “Limit reached“ switch error for the height or width plates although no mechanical problems is visible - > light
barrier defect (LED V7 or LED V8) on D1.
· No communication with D2
- D2 error or
- Serial interface on D1 faulty.

Indications of a defect inside D2 board:

· LED V20 (green, µ controller) constantly ON or OFF - > error in µ controller
· LED V25 (green, 5 V for logic) OFF
· LED V26 (green, +12V for lamp regulation) OFF
· LED V27 (green, -12V for lamp regulation) OFF
· D1 reports no communication with D2
- Serial interface on D1 faulty or
- D2 error.

2 SPECIAL TOOLS
Hex wrench, 10 mm
Hex wrench, 11 mm

3 ORDERING INFORMATION
Refer to Chapter 9

3-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/6 PROTEUS XR/A

COLLIMATOR
4 PROCEDURE
Note: Before any action, please make sure that the collimator power is disconnected.

4-1 REPLACE THE D1

4-1-1. Remove the collimator cover:

The cover is fixed with 9 screws (2 mm allen wrench).

First open the srews on the left and on the right side of the collimator (2 on each side).
Next open the 5 screws on the back side of the collimator and remove the two parts of the cover.

4-1-2. Open the collimator front panel :

The front panel is fixed with 2 screws (2.5 mm allen wrench).

Open the 2 screws on the right side and open the front panel.
The board D1 of the collimator is now visible:

D1-Board:

4-1-3 Replace the defective D1-Board:

a) Pull the following plugs from the D1-Board

D1X8
D1X9
D1X5 (which is the connector to the D2-Board)
D1X3 (CAN-Bus)
D1X1.1 and D1X1.2 (Power Supply)

b) Open the 4 screws, which are used to fix the board

(2.5 mm allen wrench)

c) If necessary replace the EPROM (D1J10)

d) Fix the new D1-Board with 4 screws (2.5 mm allen wrench)

e) Replug the connectors similar to a)

3-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/6 PROTEUS XR/A

COLLIMATOR
4-1-4 Jumper settings and calibration:

Verify the setting of the DIP switch on the D1-Board. The DIP switch S2 on the D1-board must be set as follows:
S2.1 = ON
S2.2 = OFF
S2.3 = ON
S2.4 = OFF
S2.5 = OFF
S2.6 = ON
S2.7 = ON
S2.8 = ON

Start the collimator calibration mode to get the calibration data stored in the EEPROM.

Note: Without calibration data in the EEPROM of the board D1 the collimator startup may fail.
For collimator calibration carry out the following steps:
a) Verify the DIP switch S2 on D1 (see above). It’s important that switch S2.4 is set to OFF.
b) Close the lamellas in both levels (longitudinal and transversal) manually.
c) Connect the collimator to the power supply.
d) Set dip switch S2.4 to ON
e) The collimator will start a calibration run. The lamellas will fully open to the photoelectric barriers and then
close to the minimum opening.
The calibration data will be stored in the EEPROM.
f) Verify the setting of the DIP switch on the D1-Board again. The new settings are
S2.1 = ON
S2.2 = OFF
S2.3 = ON
S2.4 = ON
S2.5 = OFF
S2.6 = ON
S2.7 = ON
S2.8 = ON
g) Now the collimator is full working.
h) Disconnect the power supply before closing the collimator.

3-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/6 PROTEUS XR/A

COLLIMATOR
4-1-5 Close the collimator front panel:

Close the front panel and fix it with 2 screws (2.5 mm allen wrench).

4-1-6 Add the collimator cover

Add the two parts of the cover to the collimator and fix it with 9 screws
(2 mm allen wrench).

4-2 REPLACING THE D2

4-2-1. Removing the collimator cover:

The cover is fixed with 9 screws (2 mm allen wrench).

First open the screws on the left and on the right side of the collimator (2 on each side).
Then open the 5 screws on the backside of the collimator and remove the two parts of the cover.

4-2-2. Removing the knobs on the front panel

Pull out the marker parts (2/Fig.1) towards the front and remove them.
Using an Allen wrench (3/Fig.1), loosen the 1.5 mm clamping screws on the knobs as shown and remove the
knobs (1/Fig.1).
Using an 11 mm hex wrench, remove the securing nuts on the potentiometer shafts and take off the snap rings.

Fig.1

3-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/6 PROTEUS XR/A

COLLIMATOR
4-2-3. Open the collimator front panel:
The front panel is fixed with 2 screws (2.5 mm allen wrench).
Open the 2 screws on the right side and open the front panel.
The board D2 on the front panel is now visible:

D2-Board: 1

Fig.2

Note: Observe ESD guidelines!

4-2-4. Replace the defective D2-Board:

a) Pull the following plugs from the D2-Board; when doing so, make sure that all connectors are labeled. If labels
are lost, label these connectors with appropriate tags.

D2X1 (connector to the D1-Board)

D2X2.1 and
D2X2.2 (lamp voltage from external power supply)
D2X4.1 and
D1X4.2 (lamp voltage to bulb)
D2X3 (fan)
D2X5 (laser)
D2X7 (display)
D2X8 (keyboard)

b) Remove the panel mounting (1/Fig.2) by removing the two 2.5 mm Allen screws (2/Fig.2), unhook the front
panel and put it down.

c) Remove the 5 cross-head screws, which are used to fix the board.

d) If necessary replace the EPROM (D2J9)

e) Remove the securing nuts and snap rings on the new D2 board.

Install the new D2 board. When doing so, make sure that the X11 pins (1/Fig.3) on the front panel are guided
exactly into the female connector on the D2. If the board is exactly installed, all the tips of the pins must be visible
from the component side of the D2X11.

3-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/6 PROTEUS XR/A

COLLIMATOR

Fig.3

f) Secure the D2 with the 5 mounting screws and replug the connectors similar to a). Install the snap rings and
securing nuts (11 mm hex).

g) Place the knobs on the potentiometer shafts and secure them using the 1.5 Allen wrench. When the knobs
are turned, they may not scratch against the front panel. Insert the marker parts.

h) Install the front panel and install the panel mounting (1/Fig.2)

4-3 REPLACE THE FUSE OR TAPE MEASURE

• Remove both side cover panels from the collimator.
• Replace the Fuse or Tape Measure

Fuse
1.6A 250V
Fuse
1.6A 250V

Tape
Measure

3-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/7 ECLIPSE PROTEUS

COLLIMATOR

subassembly: Replace the whole collimator, collimator control board, user interface board, collimator
lamp assembly, bucky centering light, LCD display, tape
purpose: version no. 1
date: 15/12/06
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

BEFORE REPLACE THE FOLLOWING PARTS, MAKE SURE ECLIPSE PROTEUS

WARNING COLLIMATOR IS POWERED OFF, OTHERWISE IT MAY RESULT IN INJURY FROM
ELECTRIC SHOCK OR OTHER HAZARDS, OR DAMAGE TO THE COLLIMATOR.

1. Replace whole collimator

Note: If the Proteus XR/a collimator is replaced with Eclipse Proteus Collimator unit, remove the
lead cup on tube side before new collimator installation.

(1) Replace the Proteus XR/a Collimator AL10F

• Demount the defective collimator from the tube
• Demount the old flange from tube
• Mount the new flange below and the new collimator on tube. Refer to chapter 2, Eclipse Proteus
Collimator Installation0
(2) Replace the Eclipse Proteus Collimator
• Demount the defective collimator from the tube
• Mount the new collimator on tube flange. Refer to chapter 2, Eclipse Proteus Collimator Installation

3-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/7 eclipse proteus collimator

2. Replace collimator control board

(1) Removing the defective control board
• Open the collimator front cover by loosening the 2 screws, one is on the top of the collimator, the
other is at the bottom.
Control board
User interface board

Fig. 1 Collimator Electrical Boards

• Unplug all the plugs of the control board

Fig. 2 Collimator Control Board

• Loosen the 4 screws which are used to fix the control board

(2) Mounting the new control board

• Mount the new control board with the 4 screws
• Reconnect all the plugs
• Close the front cover and fix the 2 screws

3-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/7 eclipse proteus collimator

3. Replace collimator user interface board

(1) Removing the defective user interface board
• Open the collimator front cover by loosening the 2 screws, one is on the top of the collimator, the
other is at the bottom.
• Unplug all the plugs of the user interface board
• Unhook the front cover and put it down

Fig. 3 Collimator User Interface Board

• Remove the knob on front panel

Loosen the screws from the knob hole

Fig. 4 Collimator Control Knob

Take off the knobs

Using an 11 mm hex wrench, remove the securing nuts on the encoder shafts and take off the
snap rings.
• Loosen the 4 screws which are used to fix the user interface board

(2) Mounting the new user interface board

• Remove the securing nuts and snap rings from the encoders shaft on the new user interface
board.
• Mount the new user interface board with the 4 screws
• Mount the securing nuts and snap rings on the new user interface board
3-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/7 eclipse proteus collimator

• Place the knobs on the encoder shafts and secure them using the 1.5 Allen wrench. When the
knobs are turned, they must not scratch against the front panel.
• Install the front cover on collimator
• Reconnect all the plugs
• Close the front cover and fix the 2 screws

4. Replace collimator lamp assembly

ONLY THE LAMP OFFERED BY GEHL WITH THE HOLDER CAN BE USED AS
WARNING REPLACED PART. OTHERWISE IT MAY CAUSE ISSUE OF LIGHT ILLUMINANCE,
EDGE CONTRAST OR LIGHT/X-RAY FIELD ALIGNMENT.

(1) Removing the defective lamp assembly

• Move the collimator right cover (1/Fig.5) and the shielding for lamp mounting hole (2/Fig.5).

Fig. 5 Collimator Lamp Exchange Cover

• Unplug the connector of the lamp

IF THE LAMP OF THE LIGHT LOCALIZER REMAINS ILLUMINATED FOR A

WARNING LONGER PERIOD OF TIME, THE HOLDER MAY HEAT UP. PLEASE AVOID
TOUCHING THE LAMP HOUSING UNTIL IT COOLS DOWN.

• Loosen 2 mounting screws of the lamp assembly from the hole on read side of the collimator and
remove the defective lamp assembly from the right side of the collimator.

Lamp exchange Hole

3-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/7 eclipse proteus collimator

• Loosen 4 screws of lamp support, take out the failed lamp. See Figure 6.

Fig. 6 Lamp Exchage

(2) Mounting the new lamp assembly
• Mount the new lamp into lamp support
• Mount the new lamp assembly on collimator
• Reconnect the connector of the lamp
• Mount the right cover of the collimator and the shielding for lamp mounting hole

To avoid damage the lamp, do not touch the bulb or inside of the reflector with bare
CAUTION hands.

3-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1 6/7 eclipse proteus collimator

5. Replace collimator bucky centering light

Fig. 6 Collimator Bucky Centering Light Mounting

(1) Removing the defective bucky centering laser equipment

• Open the collimator front cover
• Unplug the connector (1/Fig. 6) of bucky centering laser equipment
• Loosening the mounting screws, Remove the laser equipment (2/Fig. 6) from the laser support
(2) Mounting the new bucky centering laser equipment
• Insert the laser equipment into the support, fix the screw
• Reconnect the connector to user interface board
(3) Align the laser beam with light field
• Power on the collimator
• Set SID=1m, FOV=200mmX200mm
• Verify if laser line is at the transverse center of the light field
• Adjust the 2 mounting screws until the laser beam deviation to the center of the light field < 2mm
• Close the front cover and fix it with the 2 screws

6. Replace collimator LCD display

(1) Removing the defective LCD display
• Open the collimator front cover.
• Remove the user interface board, referring to step (1) of Replace collimator user interface board
above. The LCD display is now visible.
• Loosen the 4 screws which are used to fix the LCD module.

Fig. 7 Collimator LCD Module

3-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/7 eclipse proteus collimator

(2) Mounting the new LCD display
• Mount the new LCD module with the 4 screws
• Mount the user interface board, referring to step (2) of Replace collimator user interface board
above.
• Reconnect all the plugs
• Close the front cover and fix the 2 screws

7. Relace collimator tape

• Open the collimator front cover
• Remove the defective tape from the tape holder
• Put the new tape in the holder
• Close the front cover with the 2 screws

Fig. 8 Collimator Tape

3-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/10

subassembly: Table Logical Board or Table Motor Replacement

purpose: version no. 3
date: 10/10/06
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
LOCKOUT/TAGOUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

To protect the circuit boards, be sure to wear the antistatic bracelet.

CAUTION Before removing the motor from under the table, or untie the motor chain, to avoid the
injury by the potential dropping table, put the blocks kit (5137108) over the rod.

To replace the motor or logical board, perform the following steps:

1. Raise the table to highest position.
2. Power off the system and apply LOTO to the main circuit breaker. Wait 3 minutes for discharge of the DC
Bus.
3. Remove the table covers.
4. Apply the mechanical LOTO blocks kit (5137108) to the table to avoid table movement.

Kit number: 5137108

5137108-1 5137108-2 5137108-3 5137108-4

Item Block Kit Length

5137108 210mm
1 5137108-1 15mm
2 5137108-2 30mm
3 5137108-3 60mm
4 5137108-4 105mm

3-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/10

Please get different length by using different blocks according to the table’s height by the below table.

Note: Table must not be driven up and down when the blocks are put over the rod.

Item Length (Max. to Min.) Related Parts

4+3+2+1 210mm 5137108

4+3+2 195mm 5137108-4/3/2

4+3+1 180mm 5137108-4/3/1
4+3 165mm 5137108-4/3
4+2+1 150mm 5137108-4/2/1
4+2 135mm 5137108-4/2
4+1 120mm 5137108-4/1
4 105mm 5137108-4
3+2+1 105mm 5137108-3/2/1
3+2 90mm 5137108-3/2
3+1 75mm 5137108-3/1
3 60mm 5137108-3
2+1 45mm 5137108-2/1
2 30mm 5137108-2
1 15mm 5137108-1

Please refer to following examples.

Example 1: All the blocks are over the rod.

4 3 2 1

3-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/10

Example 2: The blocks 5137108-3 and 5137108-4 are over the rod.

4 3

Example 3: The block 5137108-4 is over the rod.

3-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/10

Example 4: The blocks 5137108-2 and 5137108-3 are over the rod.

3 2

Example 5: The blocks 5137108-1 and 5137108-2 are over the rod.

1 2

3-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/10

5. Disassemble the old motor from the table.

1) Unplug the cable.

CAUTION The motor is very heavy. Please be careful when removing.

2) Demount the three screws on the motor chassis with wrench.

3) Take apart the chain from the gear.

4) Remove the old motor together with the motor chassis from the table.

3-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/10

5) Demount the screws which fixing the motor and motor chassis.

6. Assemble the new motor to the table.

Note: The new motor should be sent together with a gear. If it is, please go to step 2) to assemble
the motor chassis. Otherwise, please proceed to step 1).

1) Mount the gear onto the motor shaft with rubber or wood hammer. The gear should be hammered
very close to the motor. There may be a little adjustment while fixing the chain with the gear.

Note: The width of the two sides of the gear is not equal.
The narrow side of the gear should be placed outside.

Narrow Side W ide Side

Narrow Side W ide Side

3-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/10

2) Assemble the motor onto the motor chassis.

a) Place the rubber piece on the motor chassis.

b) Fix the motor onto the motor chassis with the rubber piece between the motor and
the motor chassis.

c) Mount the screws.

d) Use flat and spring washer when necessary.

3-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/10

3) Assemble the motor onto the table.

a) Place the rubber piece on the interface between the motor chassis and the table.

Place the Place the

rubber piece rubber piece
here. here.

b) Place the motor chassis onto the rubber piece.

c) Fix the chain with the gear.

3-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 9/10

d) Partly mount the screws which fixing the motor chassis and the table.

Note: Don’t mount the screws fully. And make the motor could be shaken slightly on the table.

e) Modify the angle and position of the motor to fasten the chain by shaking.

f) Mount the screws fully.

g) Plug the cable.

3-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 10/10

7. Remove the mechanical LOTO and re-apply power to the system.

8. Check the direction of table motion when presses down the foot pedal. If the table motion is opposite with the
foot pedal, exchange the two jumpers CS3-4 and CS4-4 on logical board.

3-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 IST 023

subassembly: Bucky Installation

purpose: Installation Procedure version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 40 min
to / / to
The following procedures describe how to install the Bucky/Grid option.

To install bucky, proceed as follows:

1. Remove the table top by unscrewing four screws under the
table top.

Bucky
Cable

Rail Seats
2. Remove the four bucky rail seats. Replace the old cassette
cabinet with new bucky.

3. Reassemble the rail seats.

4. Connect bucky cable and cassette sensing tray cable to

the connectors.

5. Route the bucky cable with Ion-chamber cable through the

hole in the middle of the table. Use ty-rap to fasten the
cables with adhesive disc and make sure the bucky move
freely without any cable scratching. Then tie the cables
along with table EM lock cable.

3-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 IST 024

subassembly: Ion Chamber Installation

purpose: Installation Procedure version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 40 min
to / / to
The following procedures describe how to install the Ion Chamber/Grid option.

Ion Chamber Insertion

To insert the Ion Chamber, proceed as follows:
1. Unpack the table top by unscrewing four screws under the
table top.

2. Insert the Ion chamber into bucky and locate the Ion
chamber on the mounting bracket.

Note: Make sure the Ion chamber detectors 1,3 are

towards table head end.

Mounting Bracket
3. Fasten the four lock screws

Lock Screws

3-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 IST 024

4. Mount the Ion chamber pre-amplifier or connector box with

provided screws.
pre-amplifier
or connector
box

5. Route the Ion-chamber cable with bucky cable through the Ion-
hole in the middle of the table. Use ty-rap to fasten the chamber
cables with adhesive disc and make sure the bucky move cable
freely without any cable scratching.

3-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/7 IST 025

subassembly: Tomo-Link Installation

purpose: Installation Procedure version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 2 hours
to / / to

The following procedures in addition to the Tomo-link Service Manual (Direction: 2133821-100) describe how to
install the Tomo-Link option.
Note: The Tomo-Link assembly should be installed with the
Proteus table and XT suspension only. The system
software should be Rev1.84, or above.
1 Drive unit installation (Inboard bridge), refer to Tomo-Link
Service Manual (Direction: 2133821-100).
Note: The driver unit can only be installed on right side of
bridge.

Cut a slot
2 Cut a slot on the top of cable hose. Then insert two driver
cables (2124056 and 2132261) into hose.
Plug in these two cables and route in hose properly.

3 Tomo-link Yoke selection.

Note: There are two different Tomo-link Yokes optional for RAD 14,21 X-ray tube and MX100 X-ray tube
seperately both shipped to the sites. Pick up the matching Tomo-link Yoke according to the X-
ray tube type. (Refer to the form below)
Note: For RAD 14/21 X-ray tube, DO NOT dispose the Tomo-link Yoke 2109740-8 before finished STEP 4
in this Job Card.
X-ray tube Tomo-link Yoke matched Part Number
RAD 14/21 X-ray tube Extended Tomo-link Yoke 2352540
MX100 X-ray tube Tomo-link Yoke 2109740-8

4 For system with RAD 14 or RAD 21 X-ray tube, transfer the accessories (rubber spacer, top shim and all
screws) factory-mounted on the Tomo-link Yoke 2109740-8 to the Extended Tomo-link Yoke 2352540.
Note: For systems with MX100 tube, skip this step.
Note: The Proteus XR/a systems with Tomo are shipped with both the Tomo- link Yoke 2109740-8 and
the extended Tomo-link Yoke 2352540. But only the Tomo- link Yoke 2109740-8 is shipped with
the accessories (rubber spacer, top shim and all screws) mounted.
For systems equipped with RAD 14/ RAD 21 tube, apply the extended Tomo-link Yoke 2352540.
Remove the accessories from the Tomo-link Yoke 2109740-8 and mount the accessories to the
extended Tomo-link Yoke 2352540 before installing the Tomo-link Yoke. (See steps following)

3-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/7 IST 025

a) Demount the screws and remove the rubber spacer from the Tomo-link Yoke 2109740-8.

Transfer the accessories

(rubber spacer, top shim
and all screws) to the
Extended Tomo-link Yoke
2352540

Rubber spacer screws

top shims

b) Fit the rubber spacer to the Extended Tomo-link Yoke and mount the screws without fully fasten .
NOTE: Pay attention to leave loose the screws for Fulcrum arm alignment.

3-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/7 IST 025

c) Fix the top shim.

d) After aligned with the Fulcrum Arm (installed in step 14 of this Job Card), fasten fully the screws holding the
rubber spacer.

5 Tomo-link Yoke installation, refer to Tomo-Link Service

Manual (Direction: 2133821-100). (Selected in step 3: for
RAD 14, 21 X-ray tube, use Extended Tomo-link Yoke
GPCP No.2352540, for MX 100 X-ray tube, use Tomo-link
Yoke GPCP No.2109740-8)
Note: Remove end rubber before install Yoke.

6 Take off the table back covers and the lower right side
cover.
Note: For Tomo-link upgrade only.
Cut out two mounting slots on upper back cover.

Mount slots

3-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/7 IST 025

7 Mount Tomo control box into table base using four M4x8
screws, washers and lock washers.
Note: For Tomo-link upgrade only.

8 Mount Tomo I/F board into cabinet using two socket-head

M4x10 screws, washers and lock washers.
Note: For Tomo-link upgrade only.
Note: Find the Tomo I/F board in box # 6-8, crate #6.

9 Connect Tomo cables inside table base according to

“TOMO-LINK SYSTEM INTERCONNECTION
ILLUSTRATION” in page 10-21 and 10-22.

Route and ty-rap cable properly.

Note: For Tomo-link upgrade only.

Tomo Cables

3-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/7 IST 025

10 Install bucky connector.

Note: For Tomo-link upgrade only.

11 Install table rear cover.

12 Mount Fulcrum Tower bracket onto table using four socket-

head M8x25 screws, washers and lock washers.
13 Fulcrum Tower installation, refer to Tomo-Link Service
Manual (Direction: 2133821-100).

14 Fulcrum Arm installation, refer to Tomo-Link Service Manual

(Direction: 2133821-100).

15 Control box installation.

Mount control box on the foot end of table using socket-
head M6x16 screws and lock washers.
Note: There are two stop screws under control box.
Remove one of them to mount control box.

3-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/7 IST 025

16 Connect Tomo cables according to “TOMO-LINK SYSTEM INTERCONNECTION ILLUSTRATION” on

pages 10-21 and 22. Remove the head end table top bumper. Pull out
Route and ty-rap cable properly. the tabletop until you can see the cable entrance.
Route the cable (REA00057) according to the
Route the cable (REA00056) according to the following illustration. Use P-clamp and ty-wrap to
following illustration: fasten it.
Make sure the cable will not be broken when
you raise or lower the table.

REA00057 P-clamp Cable Entrance

REA00056

17 Tomo-link calibration, refer to Tomo-Link Service Manual

(Direction: 2133821-100).
Note: Generator Selection must be set to Advantx
Style Generator in Section 16.

3-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/7 IST 025

Note: If the X-ray beam and collimator light field are not aligned to the image receptor, you can
refer to Step 16 to adjust when necessary.

18 Tomo-link position adjustment by insertion of Adjustment

Plates.
1) Loosen the two screws on the same side of the Yoke
on which the plates should be fixed in.

2) Insert suitable sum of plates (1 to 4) into the space

between the Yoke and the rubber spacer.

Note: Please choose the proper pieces of plates to

adjust the alignment between the X-ray beam
and image receptor.

3) Fasten the screws.

19 Put the driver unit cover on.

20 Dispose the spare Tomo-link Yoke.

3-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 IST 026

subassembly: Proteus XR/a Collimator Bulb, Fan Replacement

purpose: Installation Procedure version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

Auto collimator
1. Power off the system.
2. Open the side window of collimator.
3. Replace the collimator bulb.
Note: Don’t touch bulb surface with fingers.
Use plastic cover on bulb to install it.

4. Open the left side cover of collimator, then replace the bulb
fan.
Note: This step is just used for Auto-collimator.

Manual collimator
1. Power off the system.
2. Open the rear cover of collimator.
3. Replace the collimator bulb.
Note: Don’t touch bulb surface with fingers.
Use plastic cover on bulb to install it.

3-39
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 IST 026

Proteus XR/a Automatic Collimator Bulb Replacement Note

1. The Proteus XR/a Automatic Collimator uses a special Collimator light bulb. When the
collimator lamp burns out it MUST be replaced with the replacement bulb listed in the
Proteus XR/a renewal parts section. Part number 2271727 MUST be used as a
replacement bulb. DO NOT use any other lamp as a replacement bulb as X-ray field to
Light field alignment may not meet HHS requirements.
2. The Proteus XR/a Collimator bulb is selected to have the filament in the same place in
all bulbs, and the position of this filament impacts X-ray field to Light field alignment.
This selection process allows the bulb to be replaced by the end user with no alignment
required for X-ray to Light field.
3. X-ray field to Light field is adjusted in the factory and will not be affected by bulb
replacement if the specified bulb is used as are placement. There is no field adjustment
for X-ray field to Light field alignment if another bulb is used.
4. The Proteus XR/a Collimator lamp is designed to operate at 24vac for
150hrscontinuous, other replacement bulbs will burn out very quickly as they are only
designed for 50hours continuous use at 24vac.
5. The Laser light has been aligned in the Factory. If you find the laser light needs
alignment DO NOT attempt to align the Laser with a screwdriver in the light slot with
power applied as this can cause damage to the laser electronics. The Laser is not a
field replaceable part and a new collimator should be ordered if there are problems with
the alignment or functionality.

3-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 IST 027

subassembly: APR Floppy Disk Recovery

purpose: Installation Procedure version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10 min
to / / to

Introduction
This procedure is used when APR disk being lost or broken.
Procedure
1. Prepare a new formatted (Windows 95 or DOS6.22) data floppy disk.
Note: Don’t copy system files
2. Power on the system.
3. Press Procedure Edit button.
4. Insert the system console SW disk into the floppy Disk Drive.
5. Press OK to enter Procedure edit mode. See page 5-9 in Proteus XR/a Operator
Manual (Direction 2259724-100).
6. Press Save/Retrieve button to enter Save/Retrieve menu.
7. Take out the system console disk, then insert the new formatted disk.
8. Press Save Backup button.
9. Wait until “Retrieving APR data complete” is displayed.
10. Press EXIT button to exit this menu. APR disk recovery is done.

3-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 IST 028

subassembly: OTS Console Replacement

purpose: Installation Procedure version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

Procedure
1. Remove both side covers and top cover on X-ray tube.
2. Disconnect two OTS Console cables (2259867 and 2258381 for RAD 14, 21 tube,
2378473 and 2378475 for MX100 tube, respectively).
3. Replace the OTS Console.
4. Connect two OTS Console cables.
5. Power on the system.
6. Check the display on OTS Console match the System Console.
Note: Ensure the coherent reading is same between the System Console and the
OTS Console (Check should be performed with incrementing/decrementing
technique factors from the OTS Console).
7. Power off the system.
8. Put on Tube covers.

3-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 IST 029

subassembly: System Console Replacement

purpose: Installation Procedure version no. 2
date: 10/10/2006
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to

Procedure
1. Remove and disconnect the covers and cables. This procedure is a reversed procedure of the installation.
2. Replace the System Console.
3. Repeat the installation procedure. Reference to the Job Card IST 010 and IST 011.
4. Power on the system.
5. Check the display on OTS Console match the System Console.
Note: Ensure the coherent reading is same between the System Console and
the OTS Console.
The Rev 2.14 of the System Console Software 2286799-16 can be used together with
CAUTION either the System I/F board 2375230 (Item #1 of Cabinet 1) or the System I/F Board
2259298-45 and CAN I/F Board 2259298-46.
WARNING LABELS SHOULD BE INCLUDED IN “OPEN ME FIRST” BOX. IF THEY
WARNING ARE MISSING, PLEASE ORDER A NEW CONSOLE (2259976) IN CONFORMITY WITH
REGULATION REQUIREMENTS.

3-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/5 IST 030

subassembly: Proteus XR/a Collimator Eprom update

purpose: Proteus XR/a collimator Eprom update version no. 0
date: 03/07/2001
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to
Before any action, please make sure that the collimator power is disconnected.

1. Remove the collimator cover:

The cover is fixed with 9 screws (2 mm allen wrench).

First open the srews on the left and on the right side of the collimator (2 on each side).
Next open the 5 screws on the back side of the collimator and remove the two parts of the cover.

2. Open the collimator front panel:

The front panel is fixed with 2 screws (2.5 mm allen wrench).

Open the 2 screws on the right side and open the front panel.
The two boards (D1, D2) of the collimator are now visible:

D1-Board:

3-44
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/5 IST 030

2-Board (in the front panel)

3. Update the software of the D1-Board:

Pull the Eprom from socket J10 and plug the new one which is labeled J10-D1.
Note: The Eprom fits only in one position (look for the slant sides of the Eprom and the socket).

3-45
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/5 IST 030

4. Verify the setting of the DIP switch S2 on the D1-Board:

The DIP switch S2 on the D1-board must be set as follows:

S2.1 = ON
S2.2 = OFF
S2.3 = ON
S2.4 = ON
S2.5 = ON for AL01C
S2.5 = OFF for AL01F
S2.6 = ON
S2.7 = ON
S2.8 = ON

3-46
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/5 IST 030

5. Update the software of the D2-Board:

Pull the Eprom from socket J9 und plug the new one which is labeled J9-D2.
Note: The Eprom fits only in one position
(Look for the slant sides of the Eprom and the socket).

6. Verify the setting of the DIP switch S1 on the D2-Board:

The DIP switch S1 on the D2-board must be set as follows:

S1.1 = ON
S1.2 = OFF
S1.3 = ON
S1.4 = ON
3-47
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/5 IST 030

7. Close the collimator front panel:

Close the front panel and fix it with 2 screws (2.5 mm allen wrench).

8. Add the collimator cover

Add the two parts of the cover to the collimator and fix it with 9 screws
(2 mm allen wrench).

3-48
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 IST 031

subassembly: Jedi Generator

purpose: KV Control Board replacement version no. 0
date: 23/01/03
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to
1. Load software file on Service Laptop (Refer to Job Card SW JEDI 7-4, Chapter 4).
2. If possible, download and save your local database (Refer to Job Card CAL JEDI 8-6, Chapter 4).
If you have a backup database on the site you can use it.

3. Replace the defective kV control board with the new one (Refer to Job Card D/R JEDI 17-48, Chapter 9).

Note: Pay attention to Write the existing number on the failed kV control board to the blank label, and
stick it on the new kV control board.

4. Restore Database (Refer to Job Card CAL JEDI 8-6, Chapter 4)

- Up-to-date database if available
- Most recent or originally saved Data Base if available
- Default one from the floppy delivered with the equipment in the Service Tool set.

Note: Pay attention to verify the software version and ensure its compliance with the KV control board
and X-ray tube type (refer to Job Card IST JEDI 5-2, Chapter 4).

Alternately, you may try to swap the NVRAM chip (U32) from the former to the new KV Control board to keep all
the parameters (Refer to Job Card PM JEDI 15-2, Chapter 8). If this chip is not involved in the failure or the cause
for replacement, it will allow to keep up-to-date data.

5. Calibrate:
- Perform several exposures on both focuses in several workstations, with exposure time longer than 12.5
ms
If default database was restored, it is necessary to resume room set up (refer to Job Card CAL JEDI 8-4, Chapter
4) and AEC calibration (if present) (refer to Job Card CAL JEDI 8-2, Chapter 4). Then perform the checksum
(refer to Job Card CAL JEDI 8-5,Chapter 4).

6. Save Database on the service floppy delivered with the equipment (refer to Job Card CAL JEDI 8-6, Chapter
4).

3-49
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 IST 032

subassembly: OTS
purpose: MX100 X-ray tube-Collimator Interface Plate Alignment version no. 0
date: 7/03/03
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30 min
to / / to
1. Proceed Alignment between tube and tube/collimator
interface plate.
1) Obtain the following focal spot alignment tools:
- A Collimator Alignment Tool 46-166390G1
- Hex Wrench, 46-165137P1
- An alignment tool adapter 2296120.
2) Place the Alignment tool adapter (2296120) on the tube/collimator interface plate.
3) Place the Collimator Alignment Fixture (46-166390G1) into the tool adapter ring.

4) Rotate the Collimator Alignment Fixture (46-166390G1) until the grid axis (y or x) is parallel to
the axis of the tube’s cathode/anode.

3-50
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 IST 032

5) Take an exposure with both Xs and Xl focal spot.

6) Adjusts the position of the x-ray tube relative to the tube/collimator interface plate.
7) To make tube position adjustments, loosen the four socket head cap screws (See illustration on Page 2-
63 or Page 2-68.) 1/4 turn counterclockwise. The screws retain the x-ray tube to tube/collimator interface
plate.
8) Move the x-ray tube until the cross hairs in the alignment tool window are midway between the
two focal spots displayed.

9) Make certain the concentricity of tube/collimator interface plate, OTS console bracket and tube window.
10) After adjustment, torque each of the four mounting screws to the same force.
11) Remove the Alignment Fixtures.

Note: Apply locktite to tube/collimator interface plate mount screws.

Note: Apply grease supplied underneath the edge of tube/collimator interface plate and the
inside surface of the adapter on collimator for easy movement.

3-51
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

3-52
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 4 CALIBRATION AND CONFIGURATION

SECTION 1 TABLE OF JOBCARDS CONTENTS

JOBCARD CONTENT VERSION PAGE

NUMBER
CAL 001 INTRODUCTION 0 4-3
CAL 002 SET SYSTEM CONFIGURATION 2 4-4
CAL 003 TABLE INHIBITION BUTTON SETTING AND ANTI- 0 4-7
COLLISION BUZZER FUNCTION
CAL 004 ADJUST ANTI-COLLISION SWITCHES 0 4-9
CAL 005 CALIBRATE TABLE HEIGHT LIMITATION 0 4-11
CAL 006 CALIBRATE SID CALIBRATION 1 4-12
CAL 007 CALIBRATE CASSETTE SIZE DISPLAY 1 4-24
CAL 008 WALL STAND (GPCP No. 2260354), SG100 WALL STAND 1 4-26
(GPCP No. 2225849), and SG120 WALL STAND (GPCP No.
2402562) COUNTERWEIGHT CALIBRATION
CAL 009 TOUCH SCREEN CALIBRATION 0 4-29
CAL 010 HHS TEST CALIBRATION 1 4-31
SW JEDI 7-4 SERVICE SOFTWARE USER GUIDE 1 4-32
SW JEDI 7-2 SOFTWARE DOWNLOAD / UPGRADE 1 4-40
SW JEDI 7-3 TUBE REPLACEMENT SOFTWARE PROCEDURE 0 4-44
IST JEDI 5-2 TUBE CONFIGURATION 1 4-49
CAL JEDI 8-4 WORK STATION PARAMETER 0 4-52
CAL 011 X-RAY TUBE WARM UP 0 4-59
CAL JEDI 8-2 AUTOMATED AEC CALIBRATION 0 4-60
CAL JEDI 8-5 CHECKSUM VALIDATION 0 4-83
CAL JEDI 8-6 BACKUP & RESTORE DATABASE SETUP PARAMETERS 0 4-86
CAL 012 DOSE CALIBRATION 0 4-89
CAL 013 LIGHT FIELD – X-RAY FIELD ALIGNMENT 1 4-90
(FOR PROTEUS XR/A COLLIMATOR ONLY)
CAL 014 CALIBRATE PROTEUS XR/A COLLIMATOR BULB 0 4-93
CAL 015 CALIBRATE PROTEUS XR/A MANUAL COLLIMATOR BULB 0 4-94
AND ITS VOLTAGE
CAL 016 CALIBRATE SG120 WALL STAND VERTICAL LOCKS 0 4-95

4-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank.

4-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2 JOBCARDS CONTENTS

PROTEUS XR/a 1/1 CAL 001

subassembly: Introduction
purpose: Calibration and Configuration version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 10 min
to / / to
Sequence

Calibration must be completed before functional checks to components can be performed.

Procedures
System Power On

Apply power to the Proteus XR/a system.

Document Modifications

Do not attempt to run Jedi Service Mode without first marking your Cal Users Guide manual to reflect
changes covered in the Proteus XR/a Release Notes. Failure to do so may cause some Service Mode
Units to operate incorrectly.

Note: Refer to Jedi Generator part of the Service manual.

Factory-Calibrated Proteus XR/a Systems

The majority of the system calibration was performed at the factory. Therefore, only the unchecked
procedures need to be run. Should there be any problems with any of the factory settings, we recommend
that only those units required to correct the problem be run.

4-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 CAL 002

subassembly: Set system Configuration

purpose: Calibration and Configuration version no. 2
date: 25/07/05
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to
1 INTRODUCTION:
Test if system configuration is accordance with the system hardware setting.

2 TOUCH SCREEN CONFIGURATION:

1. Press and hold the quick up/down key, at the same time power on the system until the service mode
appear on the touch screen.

2. The initial parameters were set at factory. The field engineer needs to re-calibrate the system
configuration according to requirements.
Note: The System Console Software version is 2.14.
The parameters shown in the illustration below are not the default configuration in
factory. The illustration is used only to show the interface.

4-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 CAL 002

3. Set the parameter according to following table.

No. Input/Action Remarks

1 Press Time & Date Use up/down key set system date and time.
2 Press collimator selection Select AUTO or MANUAL collimator.
3 Table selection Set table have or have not Bucky.
4 Wall Stand Set wall stand position: HEAD/ FOOT/FRONT/BACK;
Center or Offset.
5 Wall Stand Selection Set wall have (BUCKY) or have not Bucky (GRID) and sensor tray
(TRAY) or no sensor tray (NONE).
6 SID display mode Set SID unit: INCH or CM.
7 Wall Stand Select tilting Wall stand (SG100 or SG120) or non tilt Wall stand.
8 Film size display mode Set film unit is INCH OR CM, if SID unit in CM. But if SID unit is INCH,
film size unit must be INCH, film size unit on OTS must be accordance
with it.
9 High, low POS. distance Set distance between Low Auto Exposure position and High Auto
Exposure position of SG100 Wall Stand between 20-100cm (8-39inch).
(for auto exposure with Bucky in horizontal position). Default value is
40cm.
Note: The default value of High, low POS. distance set in System
Console is 40cm, which is different from the default distance
between Low Auto Exposure position and High Auto
Exposure position set on SG100 or SG120 Wall Stand (44cm).
So it’s a must to check and change the High, low POS.
distance value in System Console and ensure it to be the
same with the actual distance between Low Auto Exposure
position and High Auto Exposure position when installing the
SG100 or SG120 Wall Stand and performing the SG100 or
SG120 SID calibration, even if the positions of the Microswitch
S4 Activator Cam and Microswitch S5 Activator Cam are not
modified and be on the default positions. (refer to Job Card
IST008 in Chapter 2 and Job Card CAL006 in Chapter 4)
10 Wall Stand detent position Change the value can set wall stand detent SID display 50-200cm(20-
XT-Switch-A (B, C, D, E) set 78inch).
11 Set Table SID Detent value Set table detent value between 50-200cm(20-78inch).
12 Field Light On Time Set field light on time from 30s to 90s. (The step is 10s)
This is not applicable to the manual collimator.
13 Tomo Unit Set have or not have Tomo function.
14 Low Position Detent Set Low Auto Exposure position SID of SG100 or SG120 Wall Stand (for
auto exposure with Bucky in level) between 50-200cm (20-78inch).
15 High Position Detent Set High Auto Exposure position SID of SG100 or SG120 Wall Stand (for
auto exposure with Bucky in level) between 50-200cm (20-78inch).
16 Film Size Expand: 0.0%, Set film size increment. This function allows the FE to adjust the
1.0% or 1.5% collimator blades opening slightly.
17 Set Printer Unit Set have or not have print unit.
18 Language 9 languages can be selected. The relative APR data and APR name
should be displayed in console interface.
19 View and save error log Display error messages and save error.log to the floppy.
20 DOSE Calibration See Job Card CAL 012.
21 Press Default Display Default configuration value.
22 Press Cancel Not save the current configuration and exit this interface
23 Press Done Save the current configuration and exit the interface

4-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 CAL 002

Note: From SW version 2.07, the Wall Stand allows to be placed in 90 degrees to the table, please select
the Wall Stand position as “Front” or “Back”. Be sure to place the Wall-XT Switches on the bridge
instead of on the rail, and place the Wall Center on the rail.
4. Press DONE to confirm the calibration then go to main screen.
Press CANCEL to cancel the calibration then go to main screen.
Press DEFAULT to recover initial value.

3 OTS DETENT CODE:

1. Mount the magnet bar onto stationary rail and bridge.

Note: Please refer to the room layout in Pre-Installation Manual (2260326-100).

the wall center and table center detent code is same: the wall center and table center detent code is different:

0 1 2 3 NOTE 0 1 2 3 NOTE
0 X 0 X X Table & Wall 0 X 0 X X Table center
0 0 X 0 X Wall-XT-Switch A 0 0 X X X Wall center
X 0 X 0 X Wall-XT-Switch B 0 0 X 0 X Wall-XT-Switch A
0 X X 0 X Wall-XT-Switch C X 0 X 0 X Wall-XT-Switch B
X X X 0 X Wall-XT-Switch D 0 X X 0 X Wall-XT-Switch C
X X 0 0 X Wall-XT-Switch E X X X 0 X Wall-XT-Switch D
X X 0 0 X Wall-XT-Switch E
Note: The magnet red face upwards.

4-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 CAL 003

subassembly: Table Inhibition Button Setting and Anti-collision Buzzer Function

purpose: Configuration version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 20 min
to / / to

Introduction

This Jobcard describes how to adjust initial setting of table inhibition button and anti-collision buzzer
function. (This function is available on Rev 01 or later version PCB)

Table Inhibition Button Setting

When power on the system, the default setting of table inhibition button is on. If you want to operate the
table, you will need to deselect this button.
The following procedures describe how to adjust the initial setting of table inhibition button.

1. Power on the elevating table.

2. Raise the table to its highest position.
3. Take off the right side table cover.
4. Now, you will see a PCB board.
5. Make the Jumper on JP1 connecting the
middle pin and the empty pin. (See
following design drawing)

4-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 CAL 003

Inhibit Anti-collision Buzzer Function

The following procedures describe how to remove anti-collision buzzer function.

1. Power on the elevating table.

2. Raise the table to its highest position.
3. Take off the right side table cover.
4. Remove the Jumper on JP2.

JP2

JP1

Table logic control board 221-3010 Rev1

4-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 CAL 004

subassembly: Adjust Anti-collision Switches

purpose: Calibration and Configuration version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 40 min
to / / to
The anti-collision switches have already been adjusted at the factory. The following procedure is needed to
perform when table downward motion is prohibited or anti-collision switches don’t work.

Malfunction Analyze
1. Power on the elevating table.
2. Lower the table height, at the same time, use a force gauge to hold back table motion under each
corner of table top frame.
3. When the force exceed 45lbs, the table should stop motion, otherwise, that anti-collision switch isn’t
working correctly.

4-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 CAL 004

Procedure

Anti-
collision

Supportive
screw
Bracket
screws

Top view Bottom view

Start
Yes

Table moves Yes anti-collision

downward switches can work

No No

Loosen two bracket screws Loosen two bracket screws

slightly, then fasten the supportive slightly, then move the switch
screw underneath the anti-collision downward a little distance.
switch slowly by a medium Philip
screw driver, until hear a “Click”
sound from anti-collision switch. Table moves
No
downward

Yes
No Table moves Yes anti-collision
downward switches can work No

Fasten two
bracket screws.

Anti-collision
switch adjust-
ment complete

4-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 005

subassembly: Calibrate Table Height Limitation

purpose: Calibration and Configuration version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:
from / / from Time: 30 min
to / / to
The table height limitation calibration was already performed at the factory and the table height is from 500mm to
800mm. The following procedure should be performed in case table height does not meet specification.

Procedures
1. Open the front cover of table base.
Safety
There are two sets of switches. One set is table height
switch Limitation
limitation switch, the other set is safety switch for
switch
limitation switch in case limitation switch can’t work.

The lowest
2. Analyze whether is the highest position or the lowest position detector
position not correct, then adjust the corresponding
detector’s position of the pedal I/F board.

The highest
position detector

3. If the adjustment doesn’t work, widen the corresponding

safety switch limitation scale. Keep the safety switch
The lowest
limitation scale 10mm larger than table height
safety switch
specification to 490mm-810mm.

4. Adjust detector again. Then check whether table height The highest
meets the specification. If not, do step 2 again. safety switch

5. Fasten both limitation detectors and safety switches

Note: In case the lower safety switch is tripped, remove the

side cover to reach and press the contactor to drive
the table up.

4-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/12 CAL 006

subassembly: Calibrate SID Calibration

purpose: Calibration and Configuration version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 30 min
to / / to

Section 1 SID calibration procedure: (For systems with Table)

Note: The inaccuracy between displayed SID and real value should less than 1.7%.

1. When the table is in its’ highest position, verify that the mark
on table height potentiometer is in alignment with mark on
the rack. System
2. Open the front cabinet cover by loosing two screws I/F Board
underneath the cover.
3. Disconnect the connector J110 in system I/F board and measure
the resistance between pin1 and pin2.
When the table is in the highest position, it should be 40±10Ω.
When the table is in the lowest position, it should be 965±10Ω.
4. Check the cables are connected correctly. Refer to the
system MIS map in page 10-1.
5. Power on and check the +5VDC±5%, +/-12VDC±5% on the
system IF board.

+12V

-12V GND

+5V

+9V

TP2

TP1

4-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/12 CAL 006

6. Set table top mode using OTS console or System console.

PA3
100K TP2

TP1

Note: Ensure the switch 1, 2 of the DIP Switch in red color to be on.

DIP Switch

4-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/12 CAL 006

7. With the table in its lowest position drive to the highest position, verify the SID display
on the OTS console is changing during entire travel range without rolling over
(continuous pot).
Adjust PA1 if the SID doesn’t change.
Note: Raise the table to its highest position. Then adjust PA1 until TP1 is about 0.93V.

8. Verify the SID display on the OTS console is changing while driving the OTS up and
down.
Adjust PA3 if the SID doesn’t change.

Note: Raise the OTS to its highest position. Then adjust PA3 until TP2 is about 0.89V.

9. Drive the table to the lowest position and write down the SID value shown on OTS console. Drive the
table to the highest position. Adjust the PA1 so that the OTS console SID changes 30cm(Table height
is from 50cm to 80cm).
10. Repeat step 9 until SID changing is the same as actual moving distance.

11. Drive the OTS to the 100cm SID (from table top) using the measure tape on collimator and write
down the SID value shown on OTS console. Lower the OTS to 70cmSID (from table top) using
measure tape. Adjust the PA3 so that the OTS console SID changes 30cm.
12. Repeat step 11 until SID changing is same as real moving distance.

13. Repeat step 9 to 12 until both of table and OTS SID values changing reflect the real moving distance.

14. Adjust P5 until the right SID is displayed on the OTS console.

FOR SG100 WALL STAND SID CALIBRATION, CONTINUE WITH FOLLOWING STEPS. IF SG100 IS
NOT SELECTED, IT’S ENOUGH TO PERFORM THE STEP 1 TO 14 ONLY FOR SID CALIBRATION.

FOR SG120 WALL STAND SID CALIBRATION, SKIP TO STEP 20 DIRECTLY. IF SG120 IS NOT
SELECTED, IT’S ENOUGH TO PERFORM THE STEP 1 TO 14 ONLY FOR SID CALIBRATION.

15. Rotate the Bucky to 0°, and angulate it to 90°（horizontal）

4-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/12 CAL 006

16. Modify the Microswitch S4 Activator Cam and Microswitch S5 Activator Cam to decide the distance
between the Low Auto Exposure position and the High Auto Exposure position, write down the value
of the distance (Distance1). (When the Bucky in horizontal, there are only two positions of Bucky on
the column at which the Auto exposure can be made. Of these two positions, the lower one is
defined as the “Low Auto Exposure position”, and the higher position is defined as the “High Auto
Exposure position”. And these two positions can be modified by adjusting the Microswitch S4
Activator Cam and Microswitch S5 Activator Cam. The default distance between these two positions
is 44cm.). (Refer to Job Card IST 008, Chapter2.)

Check and ensure the parameter value in System Console to be the same with the actual distance
between Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low
POS. distance”, Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High
CAUTION Auto Exposure position set in System Console (see parameter 9 “High, low POS.
distance”, Job Card CAL 002) is 40cm, which is different from the default distance
set on SG100 Wall Stand (44cm). So it’s a must to check and change the
parameter value in System Console to ensure it to be the same with the actual
distance between Low Auto Exposure position and High Auto Exposure position
before performing the SG100 SID calibration according to the following steps, even
if the positions of the Microswitch S4 Activator Cam and Microswitch S5 Activator
Cam are not modified before and be on the default position.

17. Set Wall Stand mode using OTS console or System console. Drive the OTS console, and make it
vertically over the Bucky of SG100.

4-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/12 CAL 006

18. Insert a cassette, lower the Bucky to the Low Auto Exposure position, pull out the tray and measure
the distance from OTS to the cassette top (actual SID value) using measure tape, then insert the
tray all the way into the Bucky and adjust P4 to make the display of SID on the OTS is the same
with the actual SID. (If there is no change of SID value displayed on OTS when the Bucky moving
up and down with the tray inserted all the way into the Bucky, adjust the P4 to make the SID value
displayed on the OTS.)

Note: When the tray is pulled out, it is preset to be no SID display on OTS, not a wrong.
To see the SID display on OTS, pay attention to insert the tray all the way into the Bucky
after measured the distance from OTS to the tray.

19. Use PA2 for auxiliary adjustment.

PA2
100K
P4
100K

FOR SG120 WALL STAND SID CALIBRATION, CONTINUE WITH FOLLOWING STEPS. IF SG120 IS
NOT SELECTED, IT’S ENOUGH TO PERFORM THE STEP 1 TO 14 ONLY FOR SID CALIBRATION.

20. Rotate the Bucky to 0°, and angulate it to 90°（horizontal）

4-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/12 CAL 006

21. Modify the Microswitch S4 Activator Cam and Microswitch S5 Activator Cam to decide the distance
between the Low Auto Exposure position and the High Auto Exposure position, write down the value
of the distance (Distance1). (When the Bucky in horizontal, there are only two positions of Bucky on
the column at which the Auto exposure can be made. Of these two positions, the lower one is
defined as the “Low Auto Exposure position”, and the higher position is defined as the “High Auto
Exposure position”. And these two positions can be modified by adjusting the Microswitch S4
Activator Cam and Microswitch S5 Activator Cam. The default distance between these two positions
is 44cm.). (Refer to Job Card IST 008, Chapter2.)

Check and ensure the parameter value in System Console to be the same with the actual distance
between Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low
POS. distance”, Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High
CAUTION Auto Exposure position set in System Console (see parameter 9 “High, low POS.
distance”, Job Card CAL 002) is 40cm, which is different from the default distance
set on SG100 Wall Stand (44cm). So it’s a must to check and change the
parameter value in System Console to ensure it to be the same with the actual
distance between Low Auto Exposure position and High Auto Exposure position
before performing the SG120 SID calibration according to the following steps, even
if the positions of the Microswitch S4 Activator Cam and Microswitch S5 Activator
Cam are not modified before and be on the default position.

S4 BEHIND COVER PLATE

S5 BEHIND COVER PLATE

Microswitch S4 activator cam

Microswitch S5 activator cam

4-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/12 CAL 006

22. Set Wall Stand mode using OTS console or System console. Drive the OTS console, and make it
vertically over the Bucky of SG120.

23. Insert a cassette, lower the Bucky to the Low Auto Exposure position, pull out the tray and measure
the distance from OTS to the cassette top (actual SID value) using measure tape, then insert the
tray all the way into the Bucky and adjust P4 to make the display of SID on the OTS is the same
with the actual SID. (If there is no change of SID value displayed on OTS when the Bucky moving
up and down with the tray inserted all the way into the Bucky, adjust the P4 to make the SID value
displayed on the OTS.)

24. Use PA2 for auxiliary adjustment.

PA2
100K
P4
100K

Section 2 SID calibration procedure: (For systems with SG100 or SG120 Wall Stand, without Table)

FOR SG100 WALL STAND, FOLLOW STEPS FROM 1 TO 8.

FOR SG120 WALL STAND, FOLLOW STEPS FROM 9 TO 16.

1. Move the SG100 Wall Stand Bucky to the High Auto Exposure position, Rotate the Bucky to 0°
and angulate it to 90°（horizontal）.

4-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/12 CAL 006

2. Modify the Microswitch S4 Activator Cam and Microswitch S5 Activator Cam to decide the distance
between the Low Auto Exposure position and the High Auto Exposure position, write down the
value of the distance (Distance1). (When the Bucky in horizontal, there are only two positions of
Bucky on the column at which the Auto exposure can be made. Of these two positions, the lower
one is defined as the “Low Auto Exposure position”, and the higher position is defined as the “High
Auto Exposure position”. And these two positions can be modified by adjusting the Microswitch S4
Activator Cam and Microswitch S5 Activator Cam. The default distance between these two
positions is 44cm.). (Refer to Job Card IST 008, Chapter2.)

Check and ensure the parameter value in System Console to be the same with the actual distance
between Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low
POS. distance”, Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High Auto
CAUTION Exposure position set in System Console (see parameter 9 “High, low POS. distance”,
Job Card CAL 002) is 40cm, which is different from the default distance set on SG100
Wall Stand (44cm). So it’s a must to check and ensure the parameter value in System
Console to be the same with the actual distance between Low Auto Exposure position
and High Auto Exposure position before performing the SG100 SID calibration according
to the following steps, even if the positions of the Microswitch S4 Activator Cam and
Microswitch S5 Activator Cam are not modified and be on the default position in the
upper step.

3. Insert the tray with a cassette all the way into the Bucky.
4. Set Wall Stand mode using OTS console or System console. Drive the OTS console, and make it
vertically over the Bucky of SG100.

4-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 9/12 CAL 006

5. Verify the SID display on the OTS console is changing while driving the OTS up and down.
Adjust P4 if the SID doesn’t change.
6. Lower the Bucky to the Low Auto Exposure position, drive the OTS to 100cm to the
cassette top (pull out the tray and measure the distance from OTS to the cassette
top using the measure tape on collimator) and write down the SID value shown on
OTS console. Lower the OTS to 70cm to the cassette top (pull out the tray and
measure the distance from OTS to the cassette top using the measure tape on
collimator). Adjust the PA3 so that the OTS console SID changes 30cm.
Repeat step 5 until SID changing is the same as actual moving distance.

Note: When the tray is pulled out, it is preset to be no SID display on OTS, not a wrong.
To see the SID display on OTS, pay attention to insert the tray all the way into the Bucky
after measured the distance from OTS to the tray.

7. Ensure the Bucky to be on the Low Auto Exposure position, pull out the tray and measure the
distance from OTS to the cassette top (actual SID value) using measure tape, then insert the tray
all the way into the Bucky and adjust P4 to make the display of SID on the OTS is the same with
the actual SID. (If there is no change of SID value displayed on OTS when the Bucky moving up
and down with the tray inserted all the way into the Bucky, adjust the P4 to make the SID value
displayed on the OTS.)
8. Use PA2 for auxiliary adjustment.

PA2
100K
P4
100K

PA3
100K

4-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 10/12 CAL 006

FOR SG120 WALL STAND, FOLLOW THE STEPS BELOW.

9. Move the SG120 Wall Stand Bucky to the High Auto Exposure position, Rotate the Bucky to 0°
and angulate it to 90°（horizontal）.

10. Modify the Microswitch S4 Activator Cam and Microswitch S5 Activator Cam to decide the distance
between the Low Auto Exposure position and the High Auto Exposure position, write down the
value of the distance (Distance1). (When the Bucky in horizontal, there are only two positions of
Bucky on the column at which the Auto exposure can be made. Of these two positions, the lower
one is defined as the “Low Auto Exposure position”, and the higher position is defined as the “High
Auto Exposure position”. And these two positions can be modified by adjusting the Microswitch S4
Activator Cam and Microswitch S5 Activator Cam. The default distance between these two
positions is 44cm.). (Refer to Job Card IST 008, Chapter2.)

Check and ensure the parameter value in System Console to be the same with the actual distance
between Low Auto Exposure position and High Auto Exposure position. (see parameter 9 “High, low
POS. distance”, Job Card CAL 002)

The default value of the distance between Low Auto Exposure position and High Auto
CAUTION Exposure position set in System Console (see parameter 9 “High, low POS. distance”,
Job Card CAL 002) is 40cm, which is different from the default distance set on SG100
Wall Stand (44cm). So it’s a must to check and ensure the parameter value in System
Console to be the same with the actual distance between Low Auto Exposure position
and High Auto Exposure position before performing the SG100 SID calibration according
to the following steps, even if the positions of the Microswitch S4 Activator Cam and
Microswitch S5 Activator Cam are not modified and be on the default position in the
upper step.

4-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 11/12 CAL 006

S4 BEHIND COVER PLATE

S5 BEHIND COVER PLATE

Microswitch S4 activator cam

Microswitch S5 activator cam

11. Insert the tray with a cassette all the way into the Bucky.
12. Set Wall Stand mode using OTS console or System console. Drive the OTS console, and make it
vertically over the Bucky of SG120.

13. Verify the SID display on the OTS console is changing while driving the OTS up and down.
Adjust P4 if the SID doesn’t change.
14. Lower the Bucky to the Low Auto Exposure position, drive the OTS to 100cm to the cassette top
(pull out the tray and measure the distance from OTS to the cassette top using the measure tape
on collimator) and write down the SID value shown on OTS console. Lower the OTS to 70cm to the
cassette top (pull out the tray and measure the distance from OTS to the cassette top using the
measure tape on collimator). Adjust the PA3 so that the OTS console SID changes 30cm.
Repeat step 5 until SID changing is the same as actual moving distance.
15. Ensure the Bucky to be on the Low Auto Exposure position, pull out the tray and measure the
distance from OTS to the cassette top (actual SID value) using measure tape, then insert the tray
all the way into the Bucky and adjust P4 to make the display of SID on the OTS is the same with
the actual SID. (If there is no change of SID value displayed on OTS when the Bucky moving up
and down with the tray inserted all the way into the Bucky, adjust the P4 to make the SID value
displayed on the OTS.)

4-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 12/12 CAL 006

16. Use PA2 for auxiliary adjustment.

PA2
100K
P4
100K

PA3
100K

4-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 CAL 007

subassembly: Calibrate Cassette Size Display

purpose: Calibration and Configuration version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 30 min
to / / to
Cassette Size calibration procedure:
1. Verify the cassette sensing cable is connected correctly;
2. Verify the system communication is working and the SID display is working well;
3. Set the film size expanding to 0%. Refer to Job Card CAL 002 in page 4-4.
4. Switch the collimator mode to Auto Mode;
5. Select table bucky receptor or wall bucky receptor depending on which cassette tray is calibrating;
6. Open the front cabinet cover by loosening the two screws underneath the
cover.
7. Measure the Volt between TP5 and GND. Adjust P6 to make the Volt
being –0.84±0.01V. System
8. Measure the Volt between TP6 and GND. Adjust P7 to make the Volt I/F Board
being –0.84±0.01V.
9. Insert a 14inch(356mm) x 14inch(356mm) cassette into table bucky.
Note: Make sure the cassette is placed in correct position.
10. For calibrating longitudinal film size, adjust P10 to make Volt between
TP7 and GND being 3.33±0.01V.
11. For calibrating lateral film size, adjust P11 to make Volt between TP8
and GND being 3.33±0.01V.

Note: If there is only 14inch(356mm) x 17inch(432mm) cassette, use

14inch(356mm) side to do longitudinal film size calibration.
Then turn the cassette around and use14inch (356mm) side to
do lateral film size calibration.
R44 10K P13
100K
R41 10K P12
R40 10K 100K
TP8
P9 R45 10K P11
100K 100K
TP7
P8 P10
100K 100K
TP6
P7
100K
TP5
P6
100K

4-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 CAL 007

12. Pull out the cassette, then re-insert it. Make sure the film size display is correct. If not, redo step 10 and
11. Adjust the Volt slightly, then try it again.
Try other size cassettes. If the film size displayed is not correct, redo step 10 and 11. Adjust the Volt
slightly, then try other cassettes.
13. Measure the Volt between TP9 and GND. Adjust P8 to make the Volt being –0.84V±0.01V.
14. Measure the Volt between TP10 and GND. Adjust P9 to make the Volt being –0.84V±0.01V.
Note: Make sure the cassette is placed in correct position.

Note: The following steps also suitable to SG 100 Wall Stand.

15. Insert a 14inch(356mm) x 14inch(356mm) cassette into wall bucky.
16. For calibrating longitudinal film size, adjust P12 to make Volt between TP11 and GND being 3.33±0.01V.
17. For calibrating lateral film size, adjust P13 to make Volt between TP12 and GND being 3.33±0.01V.

Note: If there is only 14inch(356mm) x 17inch(432mm) cassette, use 14inch(356mm) side to do

longitudinal film size calibration. Then turn the cassette around and use14inch (356mm) side
to do lateral film size calibration.

R54 10K
10K

P13
R50 10K 100K
P12
R55 10K 100K
R51

P11
100K
P10
P9 100K
100K
P8
100K TP12

P7
100K TP11
P6
100K
TP10

TP9

18. Pull out the cassette, then re-insert it. Make sure the film size display is correct. If not, redo step 16 and
17. Adjust the Volt slightly, then try it again.
Try other size cassettes. If the film size displayed is not correct, redo step 16 and 17. Adjust the Volt
slightly, then try other cassettes.

4-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 CAL 008

subassembly: Wall Stand (GPCP No. 2260354), SG100 Wall Stand (GPCP No. 2225849), and SG120 Wall
Stand (GPCP No. 2402562)
purpose: Calibration and Configuration version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 20 min
to / / to

Wall Stand counterweight has been calibrated at factory. The following procedure is provided in case re-
calibration is needed.
Counterweight Calibration Procedure:

1. Open the back cover of the wall stand.

2. Open the back cover of the counterweight container.

3. Hold the counterweight container firmly and Insert the provided counterweight.
*Pull out the counterweight container with a provided puller, then change the counterweight in the container

Note: The content with a star is only for the wall stand with a knee spacer.*

4. Check the bucky up and down motion is smooth and operating force is less than 5kg when inserting a 14”x17”
cassette.
5. Mount the counterweight container cover and wall stand cover, fasten all screws.

WARNING Keep the film cabinet and counterweight pieces under control, while you are taking the
calibration procedure. Any unexpected movement may result in body hurts.

4-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 CAL 008

Counterweight Calibration Procedure For SG100 Wall Stand:

Note: The information in this page is concerted with the revision 6 of SG 100 Wall Stand Service Manual
(GPCP Number 2150297-100). For the reason of the updates and changes in that manual, it is
recommended to see also the latest Service Manual of SG 100 Wall Stand for reference.
220/110v Caution Label
1. Raise the Bucky assembly to its top position.
2. Remove the two lower trim covers (3) screws.
3. Remove the lower (charcoal grey)
counterweight cover (6 screws).
Knurled Screws –
loosen to open
Bucky Front Panel

4. Add or remove counterweights until the Bucky carriage is balanced. Lower Trim Covers

Note: Extra counterweights are furnished as part of the Ion Chamber option.

5. Raise the Bucky assembly to 63” (1.6 m) from the floor

to enable installation of the lower charcoal grey cover
and the lower trim covers. Iron Counterweights
6. Replace the charcoal grey cover and ensure that the Bucky (1.9 kg)
harness is outside the cover.
7. Reinstall lower trim covers.

Iron Counterweights

4-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 CAL 008

Counterweight Calibration Procedure For SG120 Wall Stand:

DURING THIS OPERATION, THE BUCKY CARRIAGE AND COUNTERWEIGHT

WARNING CARRIAGE CAN MOVE.

1) Move the carriage to the lowest position.

2) Remove the metal cover on the front of the column.

Metal cover

3) Remove the second metal cover to access the counterweights.

Metal cover

Counterweights

4) Place or remove the counterweights with care.

5) Reinstall the two sheet metal covers and the column lateral covers.

4-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 CAL 009

subassembly: Touch Screen Calibration

purpose: Calibration and Configuration version no. 0
date: 14/08/01
NF No. Production date Serial No. Personnel:1
from / / from Time: 30 min
to / / to

Touch Screen calibration has been performed at the factory. The following procedure is provided in case the
touch screen needs to be recalibarated.

1. Tools
- Proteus System Software Disk
- A PS2 type of computer keyboard
- A communication cable
Note: All systems are shipped with a keyboard cable. If the cable is missing, FE should make a
communication cable according to illustration.

2. Procedure
1. Power off.
2. Demount the printer if have.
3. Use the communication cable connecting the keyboard and the console connector CN1.
4. Insert the system software disk into the console.
5. Power on.
6. At the c:/ prompt type “Tbdriver.exe”
7. Type “Tbcal.exe”; enter the main menu of Touch Screen Calibration Program.

4-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 CAL 007

8. Press “H” (Hard Calibrate).

9. Touch the extreme bottom left corner and right corner, and then press any key to return main menu.
10. Press “6” (640X480 graphics).
11. Touch the centre of the crosses twice then press any key to return main menu.
12. Press”7” (Test menu) then press”6”.
13. Touch the screen, there should be an “x” under the touch area. If “x” is away from the touch area, should
check the system console.
14. Press ”x” to exit the calibration program.
15. Power off and mount the printer.

4-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 010

subassembly: HHS Test Calibration

purpose: Calibration and Configuration version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 30 min
to / / to

Installers must indicate that the combination of installed HHS Certified Components is compatible on Form
F3382 provided in Direction 46-013894, System Field-Test For HHS.

Proteus XR/a System HHS Compliance Compatibility List

PRODUCT CATEGORY PRODUCT DESCRIPTION MODEL NUMBER

X-RAY CONTROL SYSTEM CONSOLE 2259976
PROTEUS XR/a SYSTEM CABINET/ 2259937
GEN. & PDU
X-RAY TUBE ASSEMBLY RAD 14 2259981
HOUSING (CASING) RAD 21 2271627
MX 100 D2301R
BEAM LIMITING DEVICE PROTEUS XR/A AUTO COLLIMATOR 2259298-54
ECLIPSE PROTEUS COLLIMATOR 2379827
CASSETTE TRAY CASSETTE TRAY 2176788
NON-CERTIFIED DEVICE OTS CONSOLE 2259974

4-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/8 SW JEDI 7-4

subassembly: SERVICE SOFTWARE USER GUIDE

purpose: version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15 min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service laptop with floppy drive

- Service tools
- JEDI service software
- 9-wire serial cable

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

Basic knowledge of PC based computer laptop, DOS and usage of Microsoft WINDOWS.

4-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/8 SW JEDI 7-4

5 PROCEDURE

5-1 Loading Service Software on Service Laptop

The service software can be used either from the calibration diskette or from the Hard Disk Drive. We recommend
to launch it from the Hard Disk Drive for speed performance.
It can operate under DOS or Windows 95; but for software download or database backup, it is required to
run asian.exe under DOS to avoid communication problem (with the mouse, click on START, SHUTDOWN,
RESTART COMPUTER UNDER DOS MODE; see page 4-40 ”Software Download / Upgrade” Job Card).
• Power ON Service laptop. Under Windows, run the File Manager (Explore)
• Create a specific directory (e.g.: JEDI) under C:\
• Insert into the floppy drive the ”Service Software” floppy delivered with the equipment in the Service Tool set.
• Copy the file SPX_X.EXE from the floppy disk to that directory
(Double click on A:\, drag and drop on C:\ JEDI or whatever name of your directory)

5-2 Unzip software file

The floppy drive supplied with the equipment (or the upgrade kit) contains “Auto-zipped” files.
It is necessary to load those files on the hard disk drive and run them; they will unzip and create other files that
you will use.
• Double click on the SPX_X.EXE file, and verify that the new files are created:
appl.mx , boot.mx, asian.exe ,Asiane.msg and data base files.mx

5-3 Using Service Software

Safety Door
Connect Service laptop as follows: and Light
Switch (J7)
• Use the 9 pin Serial cable, part No 2207478, to connect
serial line of Service laptop to connector XJ8 on the I/F
board. Service
Terminal (J8)
• Switch on the Service laptop.
• To run the program:
Under Windows: Inside Comm-
unication (J9)
- double click on “asian.exe”
Under DOS:
- select Disk Drive from where you want to run the program: C: [enter] or A: [enter]
- enter the directory where “asian.exe” stays in.
- key in : “asian” [enter]

4-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/8 SW JEDI 7-4

The following screen appears:

• Power ON the generator

• Press function key F1
The following example screen appears:

The software will load the help screen information contained in Asiane .msg file.

4-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/8 SW JEDI 7-4

• Wait or press space bar to jump to screen.
This screen will appear:

5-4 Selecting Maintenance and Application Mode; major keys

FROM PROCEDURE TO
APPLICATION MODE Type <ALT> - <S> (Together) SETUP/MAINTENANCE MODE
MENU 3
APPLICATION MODE Type <ALT> - <D> (Together) SETUP/MAINTENANCE MODE
LAST MENU OR SUB-MENU
selected.
SETUP/MAINTENANCE MODE From any menu, type <R> (several APPLICATION MODE
types if necessary) or <Q>

[Q] Return to application mode

[R] Return to a higher level menu
[W] Validate
[ALT] & [S] (Together) Calibration mode (Menu 3)
[ALT] & [D] Calibration mode (Last menu called)
[→] and [←] In maintenance mode, to move through menus
[F1] to [F0] Function keys with action based on context.
Other keys Based on context. Main function recalled in the screen
and also in Job Cards wherever used.
<ESC> Escape Service Menu
Note: It may cause JEDI communication problem to
directly use ESC key to quit Service mode.

4-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/8 SW JEDI 7-4

5-5 Service Menu breakdown tree

• Type [ALT] & [S] (Together) to go to Maintenance Menus (MENU 3)

• Type [→] and [←] keys to select a menu.
• Illustration 1 shows the relationship between the Maintenance Mode menus and the function keys used to
access those menus.
• To return to a higher level, key in [R]
The darkened menus are the ones used for Generator and room setup (Configuration and Calibration):
menu 3, 4, 5.
Menu 3 is used to Configure the system
Menu 4 is used to calibrate AEC mode (Automatic Exposure Control)
Menu 5 is used to perform Checksum
Menu 1 is used to perform generator test and diagnostics.
Menu 2 is used to enter Date and Time, visualize/clear error log, and visualize/clear tube and generator recorded
tracking Data.

4-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/8 SW JEDI 7-4

MENU 1
[F1] [F3] [F5] [F7]
HEAT ANOD HIGH AEC

AUTO AUTO,
3,4,5 3k, 9k
NoLD GATE ShC
CD INV
Tst Tst

MENU 2
[F3] [F5] [F7]
LIST NEXP DATE

MENU 3
[F1] [F5]
TECH MOD

MENU 4
[F5] [F7]
AEC CAL

[F1] [F3] [F5] [F9]

KVEF KG KTIME KF

MENU 5
[F1] [F7]
RAMS Vx Px.x DSPL

[F1] [F3]
CKSM MCL

Illustration 1 - Service menu Breakdown tree

4-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/8 SW JEDI 7-4

5-6 Sub-Menu summary description

1. Configuration - MENU3
TECH: programming workstation, technique parameters.
MODE: Select Renard or Normal scale for kV selection.
(See Page 4-52 “Workstation Parameter” Job Card ).
2. Calibration - MENU4
AEC: To set parameters if known, or modify them manually.
CAL: To calibrate Automatic Exposure Control, for each AEC chamber and Screen-film combination.
(See page 4-60 Job Card “Automated AEC calibration”)
3. Ram - MENU5
RAMS: NVRAm operation & display:
- CKSM: To update Checksum after configuration, calibration, parameter change. (See page 4-83, Job
Card “Checksum Validation”)
- MCLR: Clear NVRam memory. Normally not to be used, unless specifically instructed. (Do not use if
Data Base backup has not been performed previously)
Vx Px.x: Display generator software version (e.g. P3.4)
DSPL: In Maintenance Mode, to display parameter after exposure using key [Z]
4. Utilities - MENU2
LIST: To display last recorded error codes (up to 64)
- Last error is visualized with Date and Time
- Function keys allow to scroll down and up
- [Z] to get back to the last recorded error
- Same consecutive error are counted Up in the same line
- [^H ], and [W] to clear error log
NEXP: To visualize/clear tube and generator recorded tracking Data. Clear must be performed only when
replacing X-Ray tube. Meaning of each parameter is found in page 4-44, ”Tube Replacement Software
Procedure” Job Card.
DATE: To enter / modify the date and time.

4-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/8 SW JEDI 7-4

5. Diagnostics - MENU1
HEAT: To exercise Heater/filament function.
- Auto: run fixed current on both filament (if 2 filaments) in sequence on selected tube (If more than 1).
- L or S: run 3, 4, or 5 Amps on Large or Small Focus.
ANOD: To exercise Rotor function.
- Auto: run rotation cycle in Low Speed then High Speed (If allowed by configuration) on selected tube.
(If more than 1)
- 3k: run one cycle acceleration, hold, break in Low Speed on selected tube (If more than 1)
- 9k: run one cycle acceleration, hold, break in High Speed (If allowed by configuration) on selected
tube (If more than 1)
HIGH: To exercise High Voltage function.
- NoLD: To troubleshoot HV problem, without mA nor rotation without X-Ray tube nor HV cable. Test is
run from 80 to max. kV, adjustable from 1 to 60 sec.
- Gate CD Test: to verify operation of the gate command board on the Inverter. Test is run during 10
sec. At 0 kV.

Note: Requires manual set up. Read related information in diagnostics section.
- ShC INV Tst: To verify operation of inverter with inverter in short circuit. Test is run during 100 msec.
At 0 kV.

Note: Requires manual set up. Read related information in diagnostics section.
AEC: To verify operation of AEC board. Refer to diagnostics section.

4-39
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 SW JEDI 7-2

subassembly: Software Download / Upgrade

purpose: This Jobcard is needed only when FE replace new version no. 1
generator , KV control board or X-ray tube. date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 1h 15 min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service Laptop with floppy drive.

- Service tools
- JEDI Service Software
- 9-wire serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

Basic knowledge of PC based computer laptop, DOS and usage of Microsoft WINDOWS.
Database backup must have been performed.

4-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 SW JEDI 7-2

5 PROCEDURE

5-1 Load Software File on Service Laptop

The service software can be used either from the calibration diskette or from the laptop hard disk drive. We
recommend launching it from the Hard Disk Drive for speed performance. It can operate under DOS, Windows 95
or Windows 3.1.
If you do not have it on the laptop, refer to page 4-32, “Service Software User Guide” Job Card.
• Power ON service laptop
Under Windows, run the File Manager (Explore)
• Create a specific directory (e.g.: JEDI) under C:\
• Insert into the floppy drive the floppy delivered with the equipment in the service tool set (or with the upgrade)
• Copy the FILE “SPX_X.EXE” from the floppy disk to that directory
(Double click on A:\, drag and drop on C:\ JEDI or whatever name of your directory)

5-2 Unzip software file

The floppy drive supplied with the equipment (or the upgrade kit) contains “Auto-zipped” files.
It is necessary to load those files on the hard disk drive and run them; they will unzip and create other files that
you will use.
• Double click on the SPX_X.EXE file, and verify that the new files are created. (appl.mx and boot.mx)

5-3 Software download

1. Power off system.

Unplug the cable from system I/F board Connector J118.
Safety Door
Connect Service laptop as follows:
and Light
Use the 9-wire serial cable, part N. 2207478, to connect Switch (J7)
serial line of service laptop to connector XJ8 on the I/F
board. Service
2. Restart the computer in DOS mode (for software download Terminal
or database backup, it is required to run asian.exe under
DOS to avoid communication problem).
Inside
With the mouse, click on START, SHUTDOWN, RESTART Comm-
COMPUTER UNDER DOS MODE.
3. Run the program:
Under DOS: -select Disk drive from where you want to run the program: C: [enter] or A: [enter]
-enter the directory where “asian.exe” stays in.
-key in : “asian” [enter]

4-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 SW JEDI 7-2

The following screen appears:

7. From the laptop software mainscreen, type “F7 : restore memory”

8. Type “appl.mx”, then enter (or C:\JEDI\appl.mx)

Note: If the system is equipped with a Rad21 tube with tube
fan, type”F80ra21f.mx” or “F65ra21f.mx”then enter.
Please refer to R21 Tube Fan Installation Manual
(2301864).
If the system is equipped with a MX100 tube, type
“F65KOUSB.mx” or “F80KOUSB.mx” then enter.
Wait for the count to start. It may take 20 seconds before
starting. The software code transfer will take about 20 minutes.
Download is complete when all the LEDs on kV Control board
are ON and laptop indicates download is complete.
Normally, the kV Control board will reset at the end of transfer
and all the LEDs will scroll.
If not, reset the kV Control board.

4-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 SW JEDI 7-2

9. Verify the software version is V5.58.
From the main screen, type F1, then ALT S and select menu 5 with the arrows.

10. Select menu 2 with the arrows, select LIST, and clear generator error log. (^H, then W)
11. To exit program, press Q, or R to return then ESC, or ESC twice.

4-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/5 SW JEDI 7-3

subassembly: TUBE REPLACEMENT SOFTWARE PROCEDURE

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15 min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service laptop with floppy drive.

- Service tools
- JEDI Service Software
- 9-wire serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

Basic knowledge of PC based computer laptop, DOS and usage of Microsoft WINDOWS.
Knowledge of Service Software (refer to page 4-32, ”Service Software User Guide” Job Card).

4-44
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/5 SW JEDI 7-3

5 PROCEDURE

5-1 Perform a Database backup

Refer to page 4-86 Job Card ”Backup & Restore Database Setup Parameters”.
1. Connect Service laptop as follows:
• Use the 9 pin Serial cable, part number 2207478, to
connect serial line of Service laptop to connector XJ8 on Safety Door
the I/F board. and Light
Switch (J7)
2. Restart the computer in DOS mode (for software download
or database backup, it is required to run asian.exe under
DOS to avoid communication problem). Service
Terminal (J8)
• With the mouse, click on START, SHUTDOWN,
RESTART COMPUTER UNDER DOS MODE.
3. Run the program: Inside Comm-
• select Disk Drive from where you want to run the unication (J9)
program: C:\JEDI [enter] or A: [enter]
• key in : “asian” [enter]
4. Save memory
• From the laptop software main screen, type “F6: save
memory”.

4-45
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/5 SW JEDI 7-3

5-2 Reset Tube Data tracking counter and error log.

1. Type ALT-S to jump to Service Menu.

2. Select menu 2 with the arrows.
3. Type F5 to select “NEXP”

Note: Before resetting all the memory, it is advised to record them on table ”Generator Counter
Reading Record” (Illustration 1).

4-46
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/5 SW JEDI 7-3

4. Enter ^H, press W to confirm.
All the tube related Data will be erased; only Generator related Data will be kept.
The filament aging parameter will be reset to default value.

5. Type Q to go back to main screen.

5-3 Verify new tube operation, clear error log

1. Run a dozen of exposures from low kV, mA, to high kV, mA in direct workstation.
2. Verify correct operation of the system.
3. Go in menu 2, LIST (F3); Clear the Error log.
4. Exit from laptop service software.
5. Run exposures from the Operating console.
6. Take necessary steps to ship the replaced tube. Include filled out table with tube information.

4-47
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/5 SW JEDI 7-3

Illustration 1 - Generator Counter Reading Record

GENERATOR COUNTER READING RECORD

Date of reading: Date of install:
Address of installation: Generator identification:
Serial number:
Software version:
Options: (AEC)
X-Ray system description:

Counter name Tube data Explanation

NO WARMUP Number of skipped Warm-up (N/A on Tiger)
RXGSF H Cumulated exposure time on small focus
RXGLF H Cumulated exposure time on large focus
RXSCOP H Cumulated exposure time in fluoro (N/A on RAD.)
ROTANOD H Cumulated Anode rotation time
NEXPSF Cumulated Number of exposure on small focus
NEXPLF Cumulated Number of exposure on large focus
N100%SF Cumulated Number of exposure on small focus at 100 % Power (N/A on
Tiger)
N100%LF Cumulated Number of exposure on large focus (N/A on Tiger)
NAMOR Cumulated Number of spits
KJSF . E Cumulated dissipated power on Small focus
KJLF . E Cumulated dissipated power on Large focus
TIME_ON H Total generator Power On time (Not erasable)
N_EXP_G H Total generator number of exposure (Not erasable)

4-48
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 IST JEDI 5-2

subassembly: TUBE CONFIGURATION

purpose: version no. 1
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15 min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service laptop with floppy drive.

- Service tools
- JEDI Service Software
- 9-wire Serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

The service laptop must be configured and software installed (refer to page 4-32 “Service Software User Guide”
Job Card).

4-49
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 IST JEDI 5-2

5 PROCEDURE

5-1 Loading Software according to tube present in the installation

Two, four or six database are available on the JEDI Service Software supplied in Service Tools depending of the
configuration:
- one for 32 kW tube: type RAD 12,(Low speed) File = F32RAD12.mx
- one for 32 kW tube: type RAD 14,(Low speed) File = F32RAD14.mx
- one for 50 kW tube: type RAD 14,(High speed) File = F50RAD14.mx
- one for 65 kW tube: type RAD 14,(High speed) File = F65RAD14.mx
- one for 65 kW tube: type RAD 21,(High speed) File = F65RAD21.mx
- one for 80 kW tube: type RAD 21,(High speed) File = F80RAD21.mx
Four database for the system equipped with tube fan:
- one for 65 kW tube: type RAD 21,(High speed) File = F65RA21F.mx
- one for 80 kW tube: type RAD 21,(High speed) File = F80RA21F.mx
- one for 65 kW tube: type MX 100,(High speed) File = F65KOUSB.mx
- one for 80 kW tube: type MX 100,(High speed) File = F80KOUSB.mx
Load from Service laptop the file corresponding to the tube present in the installation and the customer
configuration Refer to Job Card “Back-up and Restore Database Setup Parameters” CAL Jedi 8-6.
Note: When replacing the database file of RAD12, 14, 21 with database file of MX100 or in reverse,
pay attention to replace the Rotation Capacitor Set (refer to Job Card D/R JEDI 17-38 in
Section 3 of Chapter 9) and ensure its correct match with the X-ray tube type.

5-2 Verify

According to the tube used in the installation, verify:

1. If 32 kW database loaded for tube RAD 12 or RAD 14
- The maximum mA displayed on the console must be 400 mA for 80 kV.
2. If 50 kW database loaded for tube RAD 14
- The maximum mA displayed on the console must be 630 mA for 80 kV.
3. If 65kw data base loaded for tube RAD 14 or RAD 21
- The maximum mA displayed on the console must be 800mA for 80kV
4. If 80kw data base loaded for tube RAD 21
- The maximum mA displayed on the console must be 1000mA for 80kV
6. If 65 kW database loaded for tube MX100
- The maximum mA displayed on the console must be 800 mA for 80 kV.
7. If 80 kW database loaded for tube MX100
- The maximum mA displayed on the console must be 1000 mA for 80 kV.

4-50
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 IST JEDI 5-2

DO NOT USE DATABASE DOESN’T MATCH, SUCH AS 32 KW FOR 50 KW TUBE OR 50

WARNING KW FOR 32 KW TUBE.

4-51
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/7 CAL JEDI 8-4

subassembly: WORK STATION PARAMETER

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15 min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service laptop with Floppy Drive

- Service tools
- JEDI service software
- 9-wire serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

The JEDI is preprogrammed. Therefore, even if the program seems to correspond to the room parameters, it
must be double checked, for example, for AEC enable, wall Bucky enable.

4 PREREQUISITES

Service laptop must be configured and software installed (refer to page 4-32 “Service Software User Guide” Job
Card).

4-52
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/7 CAL JEDI 8-4

5 PROCEDURE

5-1 Introduction

Workstation programming uses function keys indicated on screen for the following :
• workstation select,
• tube select,
• define nominal number of exposures for 2-point mode operation,
• AEC : types of chamber and number of pickup fields in each,
• Film-screen combination select, (if only one Select A).

5-2 Calling the Subroutine

Call TECH (setup mode, menu 3, function key [F1]).

MENU3 TECH MODE

-> F1 F5

<-

R: Q:

***************** MENU3 *****************

TECH<tok_Tab>:<tok_Tab>Se
MODE<tok_Tab>:<tok

Illustration1 - Setup Mode, Menu 3

Resulting display is shown in Illustration 2.

4-53
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/7 CAL JEDI 8-4

5-3 Parameter Selection

Note: Any new parameters created must be stored in the installation report (same as Illustration 3).
1. Workstation Selection
OFF No selection
SPE * Anatomic (for RF room)
DIR* Anatomic (for RAD room)
POMU Wall-mounted Bucky (i.e. SG50 or SG70)
SETE Spot-film device technique on remote-controlled table (i.e. Prestilix 1600)
TOPO Tomography Bucky
TOSE Tomography spot-film device technique
POTA Table-mounted Bucky
PULM Pulmorapid
CHAN Film changer
TOCO Special tomographic applications
SECO Spot-film device technique on conventional table
NUME Digital mode
TONU Digital tomography

Use the [ ! ] and [ z ] keys to select.

* For RAD
TECH 1 = DIR
TECH 2 = POTA (TABLE BUCKY with moving grid) or DIR (if fixed grid)
TECH 3 = POMU (with moving grid) or DIR (if fixed grid) or OFF (if no Wall Bucky)
TECH 4 = TOPO (if existing)

Note: For systems equipped with no Table configuration, TECH1 should be set DIR, TECH2 and
TECH4 should be set OFF.

4-54
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/7 CAL JEDI 8-4

Nominal
Workstation Tube Tomo tech & time number of Type of AEC
exposures In
2-point mode

Illustration2 - Workstation Menu

2. Tube Selection

T1 Tube 1 only
3. Select the number of nominal exposures for 2-point mode operation.

Suggested values are given below:

DIR N = 2 POTA N = 2
POMU N = 2

Use function keys [F5] and [F6] to select.

4. Selection of Exposure Chamber

IN1 Ionization chamber 1 (for Table Bucky workstation POTA).

IN2 Ionization chamber 2 (for Wall Bucky Workstation on - POMU).

Select AEC in or out using function keys [F7] et [F8]. Each chamber corresponds to a specific technique, i.e.
POMU and POTA.

4-55
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/7 CAL JEDI 8-4

5. Control Console Function Key assignment

Function keys are assigned using the alphanumeric keyboard ([1] corresponds to function key 1, etc., up to 8).
Use the shift key for numbers 0 to 9.

With the RAD Console only four techniques are available.

The technique selected is shown in reverse video in zone 3.

6. Selection of screen-film combination used

Keys [A], [B] and [C] are used to select the first, second and third screen-film combinations, respectively.

The combination selected is displayed in reverse video in zone 2.

Press the key again to cancel a selection.

One combination is always selected. Select Key A for the RAD used screen film combination.
7. Selection of Number of Pickup Fields

The number of pickup fields of the exposure chamber selected for AEC Mode with ionizing chamber or II must
be keyed in:

[D] middle pick-up field (one),

[F] three pick-up fields.

The number of pick-up fields is displayed in reverse video in zone 3.

8. Validation

Use [W] to validate all values for a given function appearing on the screen.

5-4 Renard or Normal Scale for kV Selection

1. Go to Service Mode, and call Menu 3 using the arrows on the keyboard.
2. Call MODE by pressing F5.
3. Select NORMAL or RENARD Scale by pressing F5.
4. Press W to confirm.

4-56
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/7 CAL JEDI 8-4

5-5 Date & Time

To enter the Date and Time:

1. Go to Service Mode, and call Menu 2 using the arrows on the keyboard.
2. Call DATE by pressing F7.
3. Enter date (MM DD YYYY) via numeric keypad.
4. Press W to confirm.
5. Press F1.
6. Enter time (HH MM) via numeric keypad.
7. Press W to confirm.
When replacing the battery in the CPU Board, clear the year–counter display on the right hand side via F7 and F9
to confirm.

Anytime programming is modified, checksum must be validated (refer to page 4-83

NOTICE
Calibration Job Card “Checksum Validation”).

4-57
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/7 CAL JEDI 8-4

WORKSTATION SELECT
FUNCTION 1 2 3 4 5 6 7 8
WORKSTATION DIR POTA POMU TOPO OFF OFF OFF OFF
TUBE T1 T1 T1 TI
NUMBER OF
EXPOSURES IN 2 2 2 2
2-POINT MODE
TOMOGRAPHIC
UNIT USED:
Y1 T1
Y2 T2 N N N N
Y3 T3
Y4 T4
Y5 T5
TYPE
OF OUT IN1 IN2 IN1
CHAMBER
mA PLATEAU
TIME FOR - - - - -
1-POINT MODE
EXTERNAL -
WORKSTATION NO NO NO NO
COMMAND*
SCREEN-FILM
COMBINATIONS
1
A A A A
2

3
NUMBER OF
PICK-UP - 3 3 3 Number
FIELDS of cells
used
in AEC
MODE RENARD OR NORMAL kV SELECTION
ERGO FULL OR MINI ERGONOMY

Illustration3 - Workstation Parameters (Example for RAD with Wall Bucky and two Ion-chambers)

4-58
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 011

subassembly: X-ray Tube Warm Up

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 2min
to / / to

1 SUPPLIES

None.

2 TOOLS

None.

3 SAFETY PRECAUTIONS

WARNING THE ROOM SHOULD BE FREE OF A PATIENT OR PERSONNEL

4 PROCEDURE
1. Power on the system.
2. Close collimator blades or block x-ray output.
3. Take 2 exposures (30 seconds apart) with the following technique Parameters:
• Table top receptor
• Large focal spot
• 70 kV
• 200 mA at 1 sec
4. Once exposures are taken the system is ready for use.

4-59
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/23 CAL JEDI 8-2

subassembly: Automated AEC Calibration

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 1h
to / / to

QUICK AEC CALIBRATION PROCEDURE:

1. Open AECcal.xls in AEC fast Calibration disk.
2. Following the instruction in this file.

NORMAL AEC CALIBRATION PROCEDURE:

1 SUPPLIES
None.
2 TOOLS
- At least 2 cassettes of each screen (18x24 cm for Bucky or 24x30 cm)
- Sensitometer
- Densitometer
- Measuring tape
- Pocket calculator
- Plexiglass plates, 5 cm thick, to cover the range from 5 cm to 25 cm, or a plastic bucket to fill with water
- A lead sheet, 2mm thick, around 18 x 12 cm, will be useful to split 2 exposures on 1 film, or to mask a
measurement cell.
- 2 cassettes 36x43 and 18x24 for format correction.
AND
- Service tools
- JEDI service software
- 9-wire serial cable Part No. 2207478.
3 SAFETY PRECAUTIONS

WARNING BE SURE TO PERFORM TUBE WARM PROCEDURE

Standard precautions for work with ionising radiation.

4 PREREQUISITES
AEC set-up is the last step of the system calibration. In consequence:
- The positioner and tube hanger should be operational.
- The collimator should be mechanically centered, and the eventual automatic collimator adjusted.
- The X-ray generator should be completely configured.
Note: Use handswitch to make exposure. Console will not Beep.

4-60
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/23 CAL JEDI 8-2

5 PURPOSE
Application mode

7-1 Film screen

combination/identification

7-2 Films development

equipment

Service mode

7-3 AEC parameters already

known?

NO YES

MENU4/AEC/F7 MENU4/AEC/F5
7-4 Automatic: 7-6 Manual parameters
Fast calibration entry

7-5 Record AEC

parameters
Application mode

7-7 Checksum validation

Select a ionization
chamber

7-8Lateral check

YES
Other ionization chamber?

END
Illustration - OVERVIEW

4-61
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/23 CAL JEDI 8-2

JOB CARD CAL JEDI 8-2 - Automated AEC Calibration has three purposes:
• Fast AEC film calibration menu (MENU4/AEC/F7)
The main purpose of this job card is to perform a quick AEC film calibration.
This job card explains in particular how to use the “Fast calibration” Service menu of JEDI software.
• Manual entering AEC parameters menu (MENU4/AEC/F5)
For already known screen-film combinations and/or ionization chambers, the corresponding parameters, (KVEF,
KTIME, KF) and/or (KG), could be entered directly without performing the Fast Calibration.
• AEC response check
Check the good response of ionization chambers and measuring circuitry.

6 OPERATING CONDITIONS

6-1 Definition and measurement of optical density

Optical density is measured over the based fog:

• process a non-exposed film,
• read its optical density: it is the “base fog”,
• set to 0 the densitometer on this base fog.

base fog

4-62
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/23 CAL JEDI 8-2

6-2 For “AEC film calibration only”

6-2-1 Focal distance

Bucky Table Vertical Bucky

1.00 m SID normally used, according to the grid localization distance.

(most frequent:1.00, 1.50, or 1.80 m)

6-2-2 Incidence:

Orthogonal incidence.

6-2-3 X-ray field:

Minimum dimensions: Bucky: 12 x 18 cm.

Lateral
Phantom centered over the ionization central measurement cell.

6-2-4 Collimation

Automatic Collimation Manual Collimation

Action full field Open the collimator blades to cassette size

4-63
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/23 CAL JEDI 8-2

7 PROCEDURE

The goal of this section is to identify the different film/screen combinations, and classify them by sensitivity: Slow,
Medium and Fast.

7-1 Film screen combinations identification

• Ask the customer which combinations of Screen / Film he is using, and their relative sensitivities: which one is
the fastest, which one is the slowest.
• Limit to 3 the number of combinations to be exposed with the Automatic Exposure Control.
Warn the customer to operate without AEC for the other combinations.
• Fill the following table:

Screen Film Film/screen combination

Manufacturer Name Manufacturer Name

A = slowest
B
C = fastest
• Declare the number of Film/Screen combinations into JEDI: A, A and B, or A,B and C: refer to Job card CAL
JEDI 8-4.

7-2 Films development equipment

• Check that the automatic processor is available

• Check that solution concentrations and temperatures comply with the manufacturer’s specifications.
• Plot a sensitometric curve.
- All gray scale levels should be visible, and the base fog should not exceed 0.2 for the development
equipment to be correct.
- Gamma should be between 2 and 3.

4-64
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/23 CAL JEDI 8-2

SENSITOMETRIC CURVE

FIRST INSTALLATION PLANNED MAINTENANCE CHECK DATE:

FILM OPTICAL DENSITY

3.6 3.6

3.4 3.4

3.2 3.2

3.0 3.0

2.8 2.8

2.6 2.6

2.4 2.4

2.2 2.2

2.0 2.0

1.8 1.8

1.6 1.6

1.4 1.4

1.2 1.2

1.0 1.0

0.8 0.8

0.6 0.6

0.4 0.4

0.2 0.2

0 0

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21

NUMBER OF DENSITY STEPS

4-65
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/23 CAL JEDI 8-2

7-3 AEC parameters already known?

Known AEC parameters: Unknown AEC parameters

• For already known screen-film combinations • Perform the Fast Calibration.

and/or ionization chambers, the corresponding • Refer to section 7–4.
parameters, (KVEF, KTIME, KF) and/or (KG),
could be directly entered without performing
the Fast Calibration.
• Refer to section 7–6.

4-66
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/23 CAL JEDI 8-2

7-4 AEC Fast Calibration Menu (MENU4/AEC/F7)

7-4-1 Preliminary for KTIME

Enter service modes, ENU4/AEC/F5/KTIME

7-4-2-2 Preselections:
Enter Service mod MENU4/AEC/F7
• Screen-film

7-4-3 Run KVEF calibration

Run KVEF calibration
NO
7-4-3 All kV steps performed?
NO
All kV steps performed? YES

YES
7-4-4 Run KTIME calibration (if needed)
Run KTIME calibration (if needed) For each of the 4 time value
For each of the 4 time values
NO
All exposure times performed?
NO
All exposure times
YES
YES
7-4-5

Run KF calibration (if needed)

YES
YES
Other screen-film? Select screen-film
(2 more possible B, C) combination
NO

7-4-6-1
7-4-6-3
Other ionization chamber? YES
(3 more possible) Select ionization chamber
7-4-6-4
NO
Run KG calibration
END

4-67
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 9/23 CAL JEDI 8-2

• If an error occurs
- To redo an exposure after an exposure, reset by pressing Z key.
- To redo an exposure after entering the optical density, enter “0” for optical density and redo the
exposure.
- To clear optical density, press CTRL + H keys and enter the new optical density.
• Loops
- In case of one ionization chamber:
Run the KVEF and KTIME calibration for each film screen combination for the ionization
chamber.
- In case of multiple ionization chambers:
Run the KVEF and KTIME calibration for each film screen combination for one ionization
chamber.
Run only the KG calibration for the other ionization chambers using the same screen film
combination.
7-4-1 Preliminary for KTIME

• Enter in Service mode, then MENU4/AEC/F5/KTIME

• Check T values are equal to T values in the table below:

N 0 1 2 3 4 5

T 10 ms 100 ms 500 ms 1000 ms 2000 ms 3200 ms

• Validate each changed value by pressing the V key

• Press R to return to MENU4/AEC.

7-4-2 Initialization

• Enter in Service mode, then MENU4 / F7

7-4-2-1 Keys description

• <- or -> keys to select the ionization chamber to be calibrated

• F1/F2 keys to select the exposure number
• F3/F4 keys to select the focus (generally Large Focus)
• F5/F6 keys to select the kV
• F7/F8 keys to select the mAs in Renard scale
• F9/F10 keys to select Plexiglass thickness
• 0 to 9 keys to enter the optical density (target or measured)
• T key to select and modify target density

4-68
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 10/23 CAL JEDI 8-2

7-4-2-2 Preselection

• A, B or C key to select screen film type (slow, medium, fast) (if only one film-screen, select A key) The
selected film-screen key flickers.

7-4-3 KVEF parameter acquisition

AEC1 1 0,00V L 80kV 10mAs 15cm OD=0,00

Ionization Exposure AEC Focus Kilovolt Exposure Plexi Optical

Chamber Number Reference time Thickness Density

1 film, 1 exposure (bucky configuration)

• Run the first exposure proposed by the software with the 1st first value (80kV) of the kV series

• Develop the film

• Measure the optical density for the film

• Enter the associated read optical density

• Validate the value with the W key

• Run the next exposure with the new parameters calculated by the software

• Develop the film(s)

• Measure the optical density for each film or image

• Enter the associated read optical density

• Validate the value with the W key - Redo the next exposure and enter the density until the V button
flicker

• When the V button flickers, record in table para. 7–5 the mAs0 displayed and press V key

• Select the next kV step in the kV series (80kV, 100 kV, max kV, 40 kV and 60 kV). and repeat
operation

• Start the KT time calibration by pressing V key after V button lighted at the end of the first screen-film
KVEF calibration

4-69
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 11/23 CAL JEDI 8-2

7-4-4 KTIME Parameter Calibration (Exposure Time Correction)

7-4-4-1 Auto calibration

The calibration can be by-passed by pressing V key again.

AEC1 1 0,00V L 80kV 0.500ms 25cm OD=0,00

Ionization Exposure AEC Focus Kilovolt Exposure Plexi Optical

Chamber Number Reference time Thickness Density

1 film, 1 exposure (Bucky configuration)

• Set the proposed Plexiglass thickness

• Run the exposure proposed by the software with 0.5s

• Develop the film

• Measure the optical density for each film

• Enter the density measured. Validate the value with W key

• Set the proposed Plexiglass thickness

• Run the proposed exposure (1s)

• Develop the film

• Measure the optical density

• Enter the associated read optical density. Redo the exposure for other exposure time, 2s, 3.2s, 10ms

• Validate the value with the W key, after entered density value

• Validate the software calculated KTIME parameter with V key

• Select the next screen/film combination if existing and start again the KVef + KTime setting procedure
from para 7–4–1

• Press the V key again to enter the KF calibration (bypass the KF calibration, if not required by hitting V
key again)

4-70
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 12/23 CAL JEDI 8-2

7-4-4-2 Warning:

In case of film too dark, after calibration, for exposure time below 10ms, you must insert an additional step
between 0 and 10ms and remove the step at 2s.

How to proceed:

Write down manually the Kt values you obtained during automatic calibration for the step 10ms, 0.1s, 0.5s, 1s, 2s
and 3.2s in table below (see procedure to read the value in para 7.6).

Original values from the auto calibration :

Time T0=10ms T1=0.1s T2=0.5s T3=1s T4=2s T5=3.2s

Kt0 Kt1=1 Kt2 Kt3 Kt4 Kt5
Value

1/ Use the procedure in para 7.6.1.2 to change manually the T0 to T5 time values according to table below.

2/ enter in the table below the values already known (from auto calibration, table above). Note that the 2s value is
removed.

3/ Enter for T0=2ms a Kt new value which is lower than the one for T1=10ms.

4/ Run a manual exposure in application mode with an exposure time between 2ms and 10ms (ex: 120kV 10cm
of plexiglass or water).

5/ Check the film darkness and adjust the Ktnew value until the darkness result is good.

- If too dark, decrease the value.

- If too light, increase the value.

Time T0=2ms T1=10ms T2=0.1s T3=0.5s T4=1s T5=3.2s

Ktnew Kt0 Kt1=1 Kt2 Kt3 Kt5
Value

4-71
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 13/23 CAL JEDI 8-2

7-4-5 KF Parameter Calibration (Format Correction)

This procedure has to be run for only 1 ionization chamber, only for one screen / film combination only in case of
Automatic collimation.
The phantom must cover the entire field for 36x43 format cassette.
• Format coding
X-ray field depends on the cassette size and the eventual division.
It is sensed and coded by the cassette tray and sent to JEDI.

Table top

Cassette l = lateral

L=

• Rad system: format coding by Automatic collimation device for bucky

Definition formula Example Format code in Suggested

L x l (cm x cm) included in L x l (cm x cm) Service laptop KF value
range area
171-250 13 x 18 4 1.08
381-570 18 x 24 6 1.05
571-850 24 x 30 7 1.04
851-1300 30 x 40 8 1.02
1301-2000 36 x 43 9 1.00

4-72
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 14/23 CAL JEDI 8-2

7-4-5-1 Procedure

AEC1 xxxx L 60kV 10mAs 10cm CO=1,00

Ionization Format Focus Kilovolt mAs Plexi Coefficient KF

Chamber Thickness

• Load the first cassette of the list in table above

• Insert the cassette into the cassette tray
• Check the format code, if format is not recognized display is NO, load next cassette and check the format
code, if not recognized display is NO, reload the next cassette go on
• Enter the suggested KF value, in table above according to the cassette size
• Run the proposed exposure
• Develop the film
• Measure the optical density
• Modify KF according to the table below:

Optical density Multiply KF by

2.5 - 2 0.4
2 - 1.5 0.6
1.5 - 1.06 0.5
1.06 - 0.94 no change
0.94 - 0.5 1.5
0.5 - 0.3 2

• Repeat this procedure until optical density =1 ±6%

• Validate the value with the W key and the displayed format becomes ”NO” (no format)
• Repeat the sequence for the next cassette of the list.

4-73
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 15/23 CAL JEDI 8-2

7-4-6 KG Parameter Calibration (Grid Correction)

7-4-6-1 Applicability

This procedure has to be performed for 2nd ionization chamber, if it is present., and with only one screen / film
combination (the slowest for example).
In case of only one ionization chamber: Press R key to by-pass KG calibration and go to section 7–4–6–5.

7-4-6-2 Procedure

AEC2 0.00V L 80kV xxmAs 15cm OD = 0.00

Ionization AEC Focus Kilovolt mAs Plexi Optical

Chamber Reference Thickness

7-4-6-3 STEP 1

• Select the screen / film combination A

• Select the ionization chamber with the arrow keys (AEC2)
• Set the SID at the same distance used for KVEF on AEC1. If not possible, go to STEP 3.

7-4-6-4 STEP 2

• Run the proposed exposure

• Develop the film
• Measure the optical density
• Enter the optical density value
• Repeat the same operations for the next proposed exposures until the V key flickers
• When the V key flickers, press the V key (end of calibration)
• Press the R key.

4-74
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 16/23 CAL JEDI 8-2

7-4-6-5 STEP 3

Application Mode • Hit R key to return to Application mode

• Put 15 cm Plexiglass plate in front of Wall Stand (AEC2)
• Set 2 Point Mode
• Set kV to 80
• Set the backup mAs: • mAs = mAs0 x (SID)2 x 2
• mAs0 = mAs at 80 kV for AEC1 found during
KVEF calibration (see table mAs0 7–5–1)
• SID = Wall Stand SID
• Run exposure in AEC
• Develop the film
• Measure the density
Service Mode • If density < 0.94 or density > 1.06 then
• Go to MENU 4 AEC F5 (service mode)
• Select KG (Key F3)
• Select Grille 2 (Key F5/F6)
• Modify KG according to table below
• Repeat the procedure until density = 1 ±6%
• If 0.94 < density < 1.06 then
• KG value is good
• press the V key to validate

Optical density Multiply KG by

2.5 - 2 0.4
2 - 1.5 0.6
1.5 - 1.06 0.5
1.06 - 0.94 no change
0.94 - 0.5 1.5
0.5 - 0.3 2

4-75
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 17/23 CAL JEDI 8-2

7-5 Record AEC parameters

7-5-1 Procedure for mAs0 recording

mAs0 records at the end of each kV step of KVEF calibration. Fill the table below.
mAs0 reporting table:

mAs0 AEC1
Sensitivity 40 kV 60 kV 80 kV 100 kV Max kV
A
B
C

mAs0 AEC2
Sensitivity 40 kV 60 kV 80 kV 100 kV Max kV
A
B
C

7-5-2 Procedure for AEC parameters recording

Access to the AEC parameters, select the Service Mode, MENU4 / AEC / F5 and fill the table below.
AEC parameters reporting table:

KVEF [F1] key

Sensitivity 40 kV 60 kV 80 kV 100 kV Max kV
A
B
C

KTIME [F5] key

10 ms 100 ms 500 ms 1000 ms 2000 ms 3200 ms
A
B
C

4-76
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 18/23 CAL JEDI 8-2

Rad system KF [F9] key

Definition formula Example Format code in
L x l (cm x cm) included in range L x l (cm x cm) Service laptop KF value
area
171-250 13 x 18 4
381-570 18 x 24 6
571-850 24 x 30 7
851-1300 30 x 40 8
1301-2000 35 x 43 9

KG [F3] key
Image receptor #1 #2

Value

To continue the Automatic Fast Calibration, go to section 7–7, and then 7–8.

4-77
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 19/23 CAL JEDI 8-2

7-6 Manual entering AEC parameters menu (MENU4/AEC/F5)

The goals of this section are:

• Explaining how to enter manually AEC parameters instead of performing the automatic fast calibration.
• KVEF, KTIME, KG and KF parameters can be entered separately.

7-6-1 Procedure

• Call the AEC menu (MENU4 / AEC / F5)

AEC KVEF KG KTIME KF

7-6-1-1 Set KVEF

• Use the function key F1 to select sub-routine KVEF

AECV 40KV 1 a.bc

KV step screen-film KVEF

combination
1, 2 or 3
• Select screen-film combination with A, B or C keys
• Select kV step 40, 60, 80, 100, or kV max with F3/F4 keys
• Set KVEF to known value with key pad
• Validate each new setting with W key
• Press the R key when settings have been completed.

4-78
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 20/23 CAL JEDI 8-2

7-6-1-2 Set KTIME

• Use function key F5 to select sub-routine KG

AEC T N=0 T=0.5 1 a.bc

Time step # Time screen-film KTIME

combination
1, 2 or 3
• Use the following keys to select the screen-film combination: A for combination 1, B for combination 2, C
for combination3. The screen-film combination selected is displayed in reverse video
• Select time step number with F1/F2 keys. (N = 0 T = 10ms, N = 1 T = 100ms, N = 2 T = 500, N = 3 T =
1s, N = 4 T = 2s, N = 5 T = 3.2s)
• If necessary, select time with F3/F4 keys
• Set KTIME to the known value with F9/F10 keys
• Validate each new setting with the W key
• Press the R key when the settings have been completed.

7-6-1-3 Set KG

• Use the function key F3 to select sub-routine KG

AEC G GRILLE 1 KG=a.b

grid No. (from 1 to 4) KG (0.8 to 2)

• Use the function keys F5/F6 to scroll grid (grid number corresponds to the ionization chamber number).
Set KG to the known value using F9/F10 keys
• Validate each new setting with the W key
• Press the R key when settings have been completed.

4-79
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 21/23 CAL JEDI 8-2

7-6-1-4 Set KF

• Use function key F9 to select sub-routine KF

AEC F FORMAT OI KV 1.2

Format code (00 to 16) KF (0.5 to 1.50)

• Use function key F5/6 to scroll format code. Set KF to the know value using F9/F10 keys
• Validate each new setting with the W key
• Press the R key when settings have been completed.

7-7 Checksum Validation

Before exiting service mode, the checksum must be validated after settings have been completed; refer to
Calibration Job Card “Checksum Validation” CAL JEDI 8-5.

7-8 Lateral cell check

7-8-1 Goal

Check that the 3 cells have the same response.

7-8-2 Principle

Repeat this procedure for each ionization chamber.

Select successively the different cells, and verify that the mAs maximum variation range does not exceed 40%.

7-8-3 Failure root causes

• Failure in the ionization chamber pre-amplifier.

7-8-4 Procedure

• Plexiglass thickness = 10 cm
• Select one image receptor
• X-ray field should be large enough to cover the 3 cells
• Application mode
• AEC on
• density correction = 0
• film screen /film key = fastest
• 3 point mode

4-80
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 22/23 CAL JEDI 8-2

• kV = 60
• mA = 100
• mAs = 32
• Select the cell(s) and make exposure according the reporting table
• Compute the mAs variation
• Repeat the procedure for each image receptor equipped with ionization chamber.

7-8-5 If failure

• Replace the ionization chamber and restart the complete calibration process this ionization chamber.

7-9 Reporting table

7-9-1 Ionization chamber #1

Lateral cells check

Cells Post-displayed mAs variation range

mAs
C
C
C
L mAs(max) − mAs(min)
L mAs(min)
L
R Should be less than 26%
R
R
LR
LR
LR
LCR
LCR
LCR

4-81
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 23/23 CAL JEDI 8-2

7-9-2 Ionization chamber #2

Lateral cells check

Cells Post-displayed mAs variation range

mAs
C
C
C
L mAs(max) − mAs(min)
L mAs(min)
L
R Should be less than 26%
R
R
LR
LR
LR
LCR
LCR
LCR

4-82
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 CAL JEDI 8-5

subassembly: Checksum Validation

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 05min
to / / to

1 SUPPLIES

None.

2 TOOLS
- Service laptop with Floppy Drive
- Service tools Part
- JEDI service software
- 9-wire serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

Service laptop must be configured and software installed (refer to ”Service Software User Guide” Job Card).

4-83
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 CAL JEDI 8-5

5 PROCEDURE

5-1 Preliminary Remarks

Checksums must be validated at end of generator setup or whenever a parameter is

NOTICE
changed.

In the checksum validation process, the processor computes a number which is a function of all the setup
parameters. When the generator is powered up, this number is computed, i.e. the sum is ”checked”.
If the two numbers differ, the generator displays error an code, indicating that one or more parameters have
been changed since the last time the sums were checked, or that a RAM-related incident has occurred.

Note: X-ray generation is inhibited if there is a checksum error.

Note: The display Va . b on menu 5 is for the software version in the CPU board EPROMS.

4-84
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 CAL JEDI 8-5

5-2 Checksum Validation

Call RAMS (setup mode, menu 5, function key [F1]

Resulting display :

RAMS CKSM MCLR

Enter function key [F1] and [V] simultaneously.
A buzzer will sound, indicating that the sums have been checked
and OK on display screen.

MCLR is used to erase all setup parameters. Function key [F3] corresponding to this
NOTICE function, should never be used.

4-85
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 CAL JEDI 8-6

subassembly: Backup & Restore Database Setup Parameters

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

None.

2 TOOLS

- Service laptop
- Service tools
- JEDI service software
- 9-wire serial cable Part No. 2207478.

3 SAFETY PRECAUTIONS

Not applicable.

4 PREREQUISITES

1. The service laptop must be configured and the software installed (refer to ”Service Software User Guide”
Job Card)
2. All calibrations must have been completed.

4-86
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 CAL JEDI 8-6

5 APPLICABILITY

Setup parameters must be logged after the setup procedure has been completed, or whenever theses
parameters are changed. This enable service engineers to key in parameters rapidly, i.e. when changing the KV
Control Board, in the event of a battery outage.

6 PROCEDURE

6-1 CPU MEMORY BACKUP

The generator must be in application mode. The control console push buttons will be inactive during the transfer.
- Connect service laptop to XJ8 on the I/F Board.
- Power up.
- Insert the calibration floppy disk without write protection.
- From Laptop Dos, A: (It can also be run from Service Laptop Hard Disk Drive but in DOS mode).
- Type JEDI on the terminal.
- Hit [F6] to save memory.
The system ask for a file name. Default file name is A:\sv_var.mx.
- Type a file name or hit [ENTER].
During transfer, the number of sent trames is displayed.
When transfer ends, the message “Transfer successful” is displayed.
If any error is detected, the transfer stops and an error message is displayed.
See next page for list of error messages.

4-87
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 CAL JEDI 8-6

6-2 CPU Memory Restore Error Messages

All parameters stored in CPU NVRAM memory have been saved on calibration floppy disk. Therefore, in case of
change of KV Control board you can initialize CPU NVRAM by transferring data from this floppy disk.
The procedure needs to Unplug the cable from system I/F board Connector J118. Then hit [F7] instead of [F6]
in service mode to restore memory.
This procedure is also used to down load new software (File type for Database or Software is automatically
recognized).

Note: In this case, calibration floppy disk can be write-protected.

Note: Error during memory restore may cause unpredictable result. A new transfer is required.
If generator is locked, power OFF and begin again the entire memory restore procedure.

6-2-1 Error Messages

MESSAGE ERROR

Cannot open file - No floppy disk.

- Floppy write protected (backup).

File contains data. The file already exists (backup).

Delete old (y,n): If you answer ”y”, the existing fole will be erased.

Error time out - Generator OFF.

- Service Terminal not connected to generator.
- Cable to system I/F board connector J118 is connected when
restore memory.
Error communication Error during transfer. Try a new transfer from the beginning.

Note: Ensure asian.exe software is run under DOS and not

WINDOWS.

4-88
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 012

subassembly: DOSE Calibration

purpose: Set system configuration version no. 0
date: 20/2/2001
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10min
to / / to
Introduction
This is a sub-step to set system configuration
Procedures
1 See Job Card CAL 002, SET SYSTEM CONFIGURATION.
2 Press DOSE CALIBRATION, enter the interface below.

3 Select the figure you want to change, and press the Up or Down arrow button to change it.
4 Press OK or CANCEL to save or not save the new configuration and return to the upper interface.

4-89
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 CAL 013

subassembly: Light field – X ray field alignment (For Proteus XR/a Collimator Only)
purpose: Calibration version no. 1
date: 18/4/2001
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10min
to / / to

Illustration 1: collimator cover

1

Illustration 2: light visor

4-90
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 CAL 013

Introduction
The collimator had been calibrated in the factory before the shipment. The situation in shipment maybe will result
in some small variation. Therefore, if necessary, the collimator should be realigned.

Alignment light field – x-ray field

• Power off the system.

• Remove left collimator cover sheet (Illustration 1/c, side cover with ventilation slits).
• Remove shielding piece (Illustration 2/c, temperature shield above light visor).
• Loosen front counter nuts (Illustration 2/d) and the two illustrated hexagon nuts (Illustration 2/e).
• Adjust light field position with the screws (Illustration 1/d) by Allen wrench (2mm).
Attention: Use only appropriate tools not to damage screws.
Indication: Final light field position is given after fixation of screws.
• Check light field / X-ray field superposition and brightness. Repeat adjustment if not OK.
Note: The overmuch adjustment of the screws (Illustration 1/d) may affect the light intensity equality of
the light field. Apply Job Card CAL 014 to calibrate the collimator bulb to adjust the light intensity
equality when necessary.
• Fix counter nuts (Illustration 2/d) and the hexagon nuts (Illustration 2/e). Secure in the same time the screws
(Illustration 1/d).
• Mount shielding piece (Illustration 2/c). Apply it at first on the right side and swivel in the left side.
• Mount collimator cover (Illustration 1/c).

Note: After adjustment of the light field, it may be necessary to readjust the line laser.
Caution: The line laser is already adjusted at the factory. Only under the specific situation that the
deviation between the light field center and line laser could not be limited within 3mm through
adjusting the light field should the line laser be readjusted at the install sites.
For the line laser readjustments, please refer to the procedures below.
• Line laser readjustment.
1) Open the collimator front panel with the 2 screws on the right side (2.5 mm allen wrench.)
Note: Observe ESD guidelines!
2) Adjust the laser line with the two screws (2.5 mm Allen wrench) (Illustration 3 resp.
Illustration 4) to the middle of the cross hair. The laser line must not differ for more than +/-
3mm from the middle of the crosshair.

4-91
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 CAL 013

Illustration 3: line laser (old laser fixing)

Line Laser
1

Illustration 4: line laser (new laser fixing)

1
Line Laser

3) Close the front panel and fix it with 2 screws (2.5 mm Allen wrench).

4-92
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 014

subassembly: Calibrate Proteus XR/a Collimator Bulb

purpose: Calibration version no. 0
date: 18/4/2003
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10min
to / / to

Procedure

2b
1a
1b

2a

1a: adjustment screw for width

1b: clamping screw for width
2a: adjustment screw for height
2b: clamping screw for height

WARNING
DO NOT TOUCH THE BULB SOCKET CONTACTS TO AVOID SHORT CIRCUIT. TIGHTEN
THE SCREW 2B WHILE THE BULB IS SWITCHED OFF TO AVOID SHORT CIRCUIT.

4-93
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 015

subassembly: Calibrate Proteus XR/a Manual Collimator Bulb and its Voltage
purpose: Calibration version no. 0
date: 12/12/2005
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10min
to / / to

Introduction
Lamp voltage on Manual collimator is provided by OTS transformer, The main power situation on site maybe
result in improper voltage to Lamp on Collimator. The appropriate tap should be seleted on XT control board by
measuring voltage.

Tools
RMS Multimeter

Procedure
measure voltage between ground and J8 , J9, J10, J11, on XT control board, select the appropriate tap for
voltage is between 22.5VAC and 24VAC.

4-94
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 CAL 016

subassembly: Calibrate SG120 Wall Stand Vertical Locks

purpose: Calibration version no. 0
date: 30/9/2004
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 30min
to / / to

Note: If you have chosen SG120 Wall Stand as an option, please refer to the following contents.
Even if the calibration of the vertical locks is performed when the equipment leaves the factory, they can be re-
calibrated when needed.
Procedure
1. Make sure the equipment is switched OFF.
2. To access the vertical lock assembly, remove the lateral and frontal covers from the column assembly.
3. The vertical lock assembly is located between the vertical carriage and the column stand and is
accessible from the bottom behind the bucky support assembly.

4. Set the bucky carriage at the appropriate height and adjust the brakes actuating on the 2 (1 for each
brake) adjustment screws marked on the right of the figures above.
1) Rotate the screws CCW (counter-clockwise) direction to approximate the brake to the brake
surface (column stand).
2) Rotate the screw CW (clockwise) direction to separate the brake from the brake surface.
Note: A distance of 0.5mm between the brake surface and the brake can be set as a start point
for the calibration.
Note: The calibration has to be made considering there is no friction between the brakes and the
brake surface (column stand) and the noise factor.
Check there is no collision between the brakes and the brake surface and the bucky
carriage can be displaced smoothly all along the vertical whole track. Just a slight friction
between the brakes and the brake surface at any point along the vertical track could be
accepted in order to minimize the noise of brake actuation.
5. Assembly the covers removed in step 2.

4-95
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

4-96
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 5 FUNCTIONAL CHECK

SECTION Content Version Page
1 Introduction 0 5-1
2 Tools and Test Equipment 0 5-2
3 Power ON 0 5-2
4 Table 1 5-3
5 Wall Stand (GPCP No. 2260354), SG100 Wall Stand (GPCP 1 5-5
No. 2225849), and SG120 Wall Stand (GPCP No. 2402562)
6 Cassette Tray 0 5-15
7 OTS Suspension 0 5-15
CHK JEDI 38-2 Performance Checks 0 5-16
CHK JEDI 38-4 Invasive mA Measurement 0 5-28

SECTION 1
INTRODUCTION
Functional Checks describes the procedures necessary to determine whether the
Proteus XR/a system (Refer to Illustration 5-1) is operating correctly and
performing within specifications.

All the Proteus XR/a system functions should be conform to safety regulations,
local codes or other applicable standards.
• Operational Checks.
• Performance Checks.

Operational Checks may be performed by the customer or trained personnel.

These checks only indicate that the unit is functioning correctly at an operational
level. They do not indicate that the unit is performing to specification.

Performance Checks must be performed by trained personnel only. These

checks verify that the unit is performing to specification. It is recommended to
complete these checks during and after installation, during periodic maintenance,
and when the equipment is replaced or modified.

Note: Before performing Functional Checks all calibrations must be

completed. (Refer to chapter 4 Calibration).

Illustration 5-1
PROTEUS XR/a SYSTEM

5-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2
TOOLS AND TEST EQUIPMENT
In addition to the standard serviceman tool kit the following tools and test
equipment will be necessary to perform the functional checks described in this
chapter:
• DVM
• Metric Tape Measure
• KEITHLEY 35080A kV peak meter (or equivalent)
• RADCAL MDH2025 dosimeter (or equivalent) with 20x5-60 probe

SECTION 3
SYSTEM POWER ON
Note: Before this step, all electrical cable must be connected and examined

Power on the Proteus XR/a system, verify that system console’s booting
correctly.

5-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 4
TABLE
4-1 Operational Check
When the assembly and electrical connections have been completed, perform
the following tests to verify the table's travel and vertical operations. Tests for the
table's elevating function is required only for elevating table.

4-1-1 Check the Float Operation

Depress the four-way float pedal. The table top should move freely in either
direction. Release the foot pedal. This energizes the four longitudinal magnets,
locking the table top securely.

Depressing the bucky switch should release the bucky magnet, and the bucky
should move freely in the longitudinal.

4-1-2 Check the Up/Down Pedals

Double click and depress the Up and then the Down foot pedal. The following
should occur while the foot pedal is depressed:
1. The table top should start to move either up or down according to which foot
pedal is depressed.
2. The four-way float foot pedal (the outside pedals) should be INACTIVE (the
table top four-way floating action should remain locked) while the table top is
in motion.

If the table can’t move when double click and depress the Up or Down foot pedal,
please check the switch backside in the sensor.

PLEASE ACTIVE THE EMERGENCY STOP OR INHIBITION BUTTON

WARNING BEFORE DOING ANY ADJUSTMENT UNDER THE TABLE.

There should
leave a gap

Switch backside

Sensor

Adjust each switch backside; insert it into the notch of the sensor. Make sure the
switch backside won’t touch the sensor when release the foot pedal. There
should leave a gap between the switch backside and the sensor.

5-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

4-1-3 Check the Table Position

Position the table top into its approximate central position. Lower the table top
until it stops. The table top should measure approximately 500mm from the floor.
Now raise the table top until it stops. The table top should measure
approximately 800mm from the floor. Refer to Illustration 5-2.
Illustration 5-2
Table Height

800+/-10mm
max
500mm
min

If a modification in the height limits (lower and upper) is required to meet these
specifications, it is necessary to adjust the Up/Down Limit Board located at the
front of the base.

4-1-4 Adjusting the Up/Down Limit Board

See table height limitation calibration

5-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 5
WALL STAND, SG100 WALL STAND, AND SG120 WALL STAND
5-1 Wall Stand (GPCP No. 2260354)

1. Depress the handle button, Wall Bucky should be able to move up and down
freely and locks in place when released.

2. Check the bucky up and down motion is smooth and operating force is less
than 5kg when inserting a 14”x17” cassette. If not, go to the Job Card CAL 008-
Wall Stand (GPCP No. 2260354), SG100 Wall Stand (GPCP No. 2225849), and
SG120 Wall Stand (GPCP No. 2402562) counterweight calibration.
Illustration 5-1

5-2 SG100 Wall Stand (GPCP No. 2225849)

Note: The information in this section is concerted with the revision 6 of SG100 Wall Stand Service
Manual (GPCP Number 2150297-100). For the reason of the update and change in that manual, it is
recommended to see also the latest Service Manual of SG 100 Wall Stand for reference.

5-2-1 Vertical Locks

With power on: using the vertical lock handle, release the mechanical and
electro-mechanical vertical locks, then verify that the carriage can move freely
and smoothly over its entire range of travel with minimum side play.

If the carriage remains locked when the mechanical lock is released, check the
lock board feeding the electro-mechanical lock (Refer to Form 1).

5-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Form - 1 Lock Board Functional Checks

LOCK FAILURE CHECK
Vertical Locks do not engage when releasing lock handle. 24 VDC between TP-9 and TP-10.
Locks remain engaged when operating lock handle. Handle microswitch or relay K11.
Locks release is delayed when operating lock handle. Relay K14.
Angulation Lock remains engaged when pressing pushbutton. 24 VDC between TP-9 and TP-10 or
pushbutton.

If carriage motion is not smooth and free, ensure that counterweights and trim
covers are installed correctly. Add or remove counterweights until
counterbalance is achieved. (Refer to Job card CAL 008, Wall Stand (GPCP No.
2260354), SG100 Wall Stand (GPCP No. 2225849), and SG120 Wall Stand
(GPCP No.: 2402562) in Chapter 4.)

Note: The carriage is counterbalanced when leaving the factory, however, if necessary,
Apply further counterweights to achieve the counterbalance (Refer to Job Card
CAL 008, Chapter 4).

Release the lock handle partially to engage the electro-mechanical locks. Verify
that the electro-mechanical locks engage before the mechanical lock
(approximately 1 mm before the mechanical lock engages). If the locks do not
engage, check the lock board. (Refer to Form1).

Release the lock handle all the way and verify that the mechanical lock’s teeth
fully engage. If not, check for misalignment, wear etc., and perform the
appropriate corrective action.

5-2-2 Bucky Angulation

Push one of the angulation lock pushbuttons on either side of the Bucky support
(and slightly rock the Bucky assembly if necessary) to release the angulation lock.
Verify that the angulation lock releases and that the Bucky can tilt forward 20o and
backward 90o freely and smoothly.
Illustration 5-2
Bucky Vertical (0o) Position Bucky Horizontal (90o) Position

If angulation motion is not satisfactory, check the condition of the bearings at the
Bucky pivot point in the Bucky support assembly.

If the angulation lock does not release, check the lock board. (Refer to Form 1).

Release the angulation lock pushbutton and verify that the angulation lock
engages, preventing further angulation of the Bucky. If the lock does not hold or it
binds, check the lock hardware for misalignment, wear etc., and perform the
appropriate corrective action.
5-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

5-2-2-1 Microswitch Actuation

Microswitch S1 should be actuated when the Bucky is within 10° of vertical.

Microswitch S3 should be actuated when the Bucky is within 10° of horizontal.
Illustration 5-3

Note: Vertical Bucky Stands not equipped with an automatic collimator do not have
microswitches S1 and S3.

5-2-3 Bucky Rotation

With the rotation lock lever, release the rotational lock and verify that the Bucky can
be easily ratated from 0o to 180o (upright to upside down).
Reapply the rotation lock and verify that Bucky rotation is not possible. If the lock
does not engage properly, check the lock hardware for misalignment, wear etc.,
and perform the appropriate corrective action.
Illustration 5-4

If the lock mechanism slips, it allows the bucky to rotate. Use the following
procedure to adjust the arm assembly. If the brake pad is too worn and the lock

5-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

mechanism still moves after making several adjustment attempts, the whole arm
assembly must be replaced.

Adjustment Lock Procedure

The adjustment of the rotation lock mechanism is performed by adjusting the two
threaded rods located inside the rotation lock system. These two rods push
against the lock cam enabling the desired adjustment.

Remove the two screws that hold the lock arm assembly using a 2.5 mm Allen
key.

Illustration 5-5

2. Remove the arm assembly and brake pad.

DO NOT ROTATE ARM ASSEMBLY. REMOVE THE BRAKE PAD CAREFULLY AS IT CAN
WARNING FALL INTO THE SG RATATION BOX AND WOULD BE IMPOSSIBLE TO RECOVER.

Illustration 5-6

5-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3. Adjust the threaded rods so that there is only enough movement between the brake pad and the arm to be able
to lock the brake assembly. Use a 1.5 mm Allen key.

Illustration 5-7

4. Re-insert the brake pad and arm assembly in position and check to ensure there is no rotation movement. This
adjustment may have to be done several times until there is no movement.

5. Once adjusted, apply loctite to threaded rods and re-insert brake pad and arm assembly.

Illustration 5-8

6. Re-insert the two screws removed in step 1 and retighten.

5-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

5-2-3-1 Microswitch Actuation

Microswitch S2-1 should be actuated when the Bucky is at 0o.

Microswitch S2-2 should be actuated when the Bucky is at 180o.

Note: Vertical Bucky Stands not equipped with an automatic collimator do not have microswitches
S2-1 and S2-2.

Illustration 5-9

Position of microswitches S1, S2, S3 Detail, S3

S2-2 is found in an analogous position 180° from S1 is found in the same location on the other side of the
that shown (See also Illustration 5-10) notched plate. Its activator cam is at the other extreme
of the notched plate’s rotation.

5-2-4 Vertical SID Points/Sitting Position

Rotate the Bucky to 0. and angulate it to 90. (horizontal), then fold down the foldable legs and lower the Bucky to
the floor. Verify that microswitch S5 is actuated when the Bucky legs touch the floor. (The Bucky is at the far
vertical SID point).

Raise the Bucky and verify that microswitch S4 is actuated when the Bucky reaches the near vertical SID point
(normally the point at which the Bucky front panel surface is at the same height as the table).

(Refer to Illustration 5-10)

Note: Vertical Bucky Stands not equipped with an automatic collimator do not have microswitches S4
and S5.

5-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 5-10

5-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

5-3 SG120 Wall Stand (GPCP No. 2402562)

5-3-1 Vertical Locks

5-3-1-1 With power on

Using the vertical lock handle, release the electromechanical vertical locks, then verify that the carriage can move
freely and smoothly over its entire range of travel with minimum side play.
If the carriage remains locked when the electromechanical lock is released, check the lock board feeding the
electromechanical lock (see Table 1 below).
If carriage motion is not smooth and free, ensure that counterweights and trim covers are installed correctly. Add
or remove counterweights until counterbalance is achieved.

Note: The carriage is counterbalanced on leaving the factory, however, if necessary add further
counterweights to achieve the counterbalance.

5-3-2 SG120 Buckyk Angulation

5-3-2-1 Angulation lock

Push one of the angulation lock push buttons behind the front panel to release the angulation lock. Verify that the
angulation lock releases and that the Bucky can tilt forward 20 degrees and backward 90 degrees freely and
smoothly (Illustration 5-11).
If angulation motion is not satisfactory, check the condition of the bearings at the Bucky pivot point in the Bucky
support assembly.
If the angulation lock does not release, check the lock board.
Release the angulation lock push button and verify that the angulation lock engages, preventing further angulation
of the Bucky. If the lock does not hold or it binds, check the lock hardware for misalignment, wear etc... and
perform the appropriate corrective action.

5-3-2-2 Micro switch Actuation

- Micro switch S1 should be actuated when the Bucky is within 10 degrees of vertical.
- Micro switch S3 should be actuated when the Bucky is within 10 degrees of horizontal.

Illustration 5-11

Bucky vertical (0 degree) position Bucky Horizontal (90 degree) position

5-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

5-3-3 SG120 Bucky Rotation

5-3-3-1 Rotation Lock

With the rotation lock lever, release the rotational lock and verify that the Bucky can be easily rotated from 0
degrees to 180 degrees (upright to upside down, Illustration 5-12).
Re-apply the rotation lock and verify that Bucky rotation is not possible. If the lock does not engage properly,
check the lock hardware for misalignment, wear etc... and perform the appropriate corrective action.

5-3-3-2 Micro switch Actuation

- Micro switch S2-1 should be actuated when the Bucky is at 0 degrees.
- Micro switch S2-2 should be actuated when the Bucky is at 180 degrees.

POSITIONS OF MICROSWITCHES S1, S2, S3

5-3-3-3 Rotation way check

Note: To realize a Right hand configuration and correct rotation way, please refer to IST009 of
Bucky Reversal Procedure.

5-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

5-3-4 Vertical SID Points / Sittings Position

Rotate the Bucky to 0 degrees and angulate it to 90 degrees (horizontal). Verify that micro switch S5 is actuated
when the Bucky is at the far vertical SID point.
Raise the Bucky and verify that micro switch S4 is actuated when the Bucky reaches the near vertical SID point
(normally the point at which the Bucky front panel surface is at the same height as the table).

S4 BEHIND COVER PLATE

S5 BEHIND COVER PLATE

Microswitch S4 activator cam

Microswitch S5 activator cam

POSITIONS OF MICROSWITCHES S4, S5

5-3-5 Bucky Grid Check

Take an exposure with the vertical bucky stand selected.

The bucky grid should oscillate. Oscillation is distinctly audible and causes slight vibration of the bucky support
assembly.
Observe the film for quality. If shading or objectionable grid lines appear, check alignment with the tube for proper
local distance setting.

5-3-6 Control Board Check

Check the control board only in the case of failure of the electromechanical locks. See Table 1 below for checks.

TABLE 1
LOCK BOARD FUNCTIONAL CHECKS
LOCK FAILURE CHECK
Locks do not engage when 24 VDC in D3 or Q2
equipment is switched on
Vertical Locks remain engaged when Handle switch
operating lock handle
Locks do not engage when Handle switch
releasing lock handle
Angulation Locks remain engaged when 24 VDC in D3 or Q1/Q3
operating lock handle

5-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 6
CASSETTE TRAY
1. Confirm the pull-out and pull –in movement is smooth.
2. Pull out the cassette tray, insert a film cassette, then fasten the cassette lock.
Check the cassette size displayed on OTS console and collimator is correct.
3. If not, see Chapter 3-“cassette size calibration”.

SECTION 7
OTS SUSPENSION
As part of the functional check of the Proteus XR/a system, also perform the
functional checks for the OTS Suspension as found in the OTS Suspension
Service Manual 2277285-100 chapter 3 Functional Checks.

5-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 8
JEDI GENERATOR

PROTEUS XR/a (JEDI 50Plus R 1T & JEDI 80R1T) 1/12 CHK JEDI 38-2

subassembly: Performance Checks

purpose: version no. 0
date: 27/ 3/ 2000
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 35min
to / / to

1 SUPPLIES

Not applicable.

2 TOOLS

Service tool.
KEITHLEY 35080A kV peak meter.
RADCAL MDH 2025 dosimeter with 20x5-60 probe.

3 SAFETY PRECAUTIONS

Standard precautions for work with ionizing radiation.

4 PREREQUISITES

All calibrations must have been completed.

5-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/12 CHK JEDI 38-2

5 GENERATOR PARAMETER ACCURACY

The precision of setting of all parameters (kVp, mA, exposure times, mAs) is checked, at variable settings of kVp,
first in Three Point mode and then in Two Point mode.

Note: kVp values are measured using kV peak meter Keithley 35080A.

5-1 Post Display

Values for mA, exposure times, and mAs are displayed on the CONSOLE after each exposure.

5-2 Accuracy Checks

5-2-1 Summary

Test exposures are made at specified settings, first in Three Point mode, then in Two Point mode, (without the
use of AEC, Automatic exposure Control). The values of parameters read during the exposure are noted and
compared with specified limits.
In each mode, exposures are made first with the small focal spot, then with the large focal spot, at kVp values of
60, 80, and 120 kVp.
In Three Point mode, each exposure is made at 20 mAs, and exposures are made with different values of mA and
exposure time at each kVp value.
In Two Point mode, exposures are made with different values of mAs at each kVp value.
The parameters to be set for each exposure are specified in Illustrations 1, 2, 3, and 4 of this document.

5-2-2 Procedure

Refer to Illustrations 1, 2, 3, 4.

Make a series of exposures corresponding to the values specified in the tables, and note the actual parameters
displayed for each exposure in the spaces provided.

For each parameter and each exposure, the tables specify acceptable high and low values.

CAUTION The measurements of mA, mAs and ms must be made using the post display
of the Service laptop. For kVp values, use the Keithley 35080A.

5-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/12 CHK JEDI 38-2

5-3 Reproducibility and Linearity of exposures

5-3-1 Summary

Reproducibility and linearity are checked by making a series of exposures, measuring the actual dose produced in
each case. The results are used to calculate coefficients of variation (C) and linearity (L).
Record values in Illustration 5.
Measurements are made using a RADCAL MDH 2025 dosimeter, with the probe (20x5-60) positioned at 100 cm
(39 inches) from the focal spot.

CAUTION The measurements of mAs must be made using the post display of the Console

5-3-2 Reproducibility checks - Procedure

1. Position the probe as specified above.

2. Make ten exposures with the following conditions:
- Three Point mode,
- no AEC
- Large focal spot
- kVp 70 kVp
exposure time 200 mS
mA 100 mA

Note: Take care not to saturate the ionization cell. The maximum output dose permitted with the 20x5-
60 probe is 3.3 mR/ms.
3. For each exposure, note the measured dose (mR), and the mAs value shown on the POST DISPLAY in the
space provided in Illustration 5.

5-3-3 Linearity checks - Procedure

1. Position the probe as specified above.

2. Make ten exposures with the following conditions:
- Three Point mode,
- no AEC
- Large focal spot
- kVp 70 kVp
exposure time 200 mS
mA 125 mA

Note: Take care not to saturate the ionization cell. The maximum output dose permitted with the 20x5-
60 probe is 3.3 mR/ms.
3. For each exposure, note the measured dose (mR), and the mAs value shown on the POST DISPLAY in the
space provided in Illustration 5.

5-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/12 CHK JEDI 38-2

5-4 Coefficients of Variation and Linearity

5-4-1 Reproducibility - Coefficient of Variation C

The coefficient of Variation, C, is defined as:

1 n
(Ri − Rm ) 2
C=
Rm
∑
i =1 n −1
where:
Ri = dose measured during exposure i

Rm = average dose measured over ten successive exposures taken

under the same conditions in less than an hour

n = number of exposures (ten)

Make the calculation and enter it into Illustration 5.

5-4-2 Coefficient of linearity L

The coefficient of Variation, L, is defined as:

Xm1 − Xm2 Rm1 Rm2
L= Xm1 = and Xm2 =
Xm1 + Xm2 A1 A2

where:
Rm1 = average dose measured over ten successive exposures taken
under the same conditions (in particular with the same value of mA,
here 100 mA), in less than an hour

Rm2 = average dose measured over ten successive exposures taken

under the same conditions (in particular with the same value of mA,
here 125 mA), in less than an hour

A1 = the mAs value used during the exposures used to measure Rm1
(here 20 mAs)
A2 = the mAs value used during the exposures used to measure Rm2
(here 25 mAs)
Make the calculation and enter it into Illustration 5.

5-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/12 CHK JEDI 38-2

5-4-3 Acceptance Criteria

The results should give:

- Reproducibility C < 0.05
- Linearity L < 0.1

6 AUTOMATIC EXPOSURE CONTROL (AEC)

6-1 Reproducibility

Reproducibility is checked in Single Point, Two Point, and Three Point modes of operation. In each case, ten
exposures are made and the doses are recorded. A coefficient of variation is calculated, as defined in section 5–
4.

6-1-1 Two Point Mode

1. Select a workstation which uses AEC.

2. Select the large focal spot .

3. Using two point mode, set the kVp to 120 kVp, mAs to 20 mAs.
4. Select the central measurement cell.
5. Center a phantom under the X-ray tube (10 to 20 cm (4 to 8 inches) of Plexiglass or water).
6. Center the probe (20x5-60) of a RADCAL MDH 2025 dosimeter 100 cm (39 inches) from the focal spot.
7. Make ten exposures. After each exposure note the dose (mR) in the space provided in Illustration 6.

Note: Take care not to saturate the ionization cell. The maximum output dose permitted with the 20x5-60
probe is 3.3 mR/ms.

6-1-2 Three Point Mode

Repeat the complete procedure specified above for Two Point mode, but use Three Point mode at 70 kVp, 250
mA, and 1000 ms.

5-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/12 CHK JEDI 38-2

6-2 Maximum mAs

This procedure checks the limitation on maximum mAs. When kVp is equal to or greater than 50 kVp, the mAs
value should not exceed 600 mAs.
1. Select a workstation which uses AEC.

2. Select the large focal spot .

3. Use Three Point mode, using values of 80 kVp, 160 mA, and 4000 ms (640 mAs).
4. Close the collimator.
5. Make an exposure.
6. Check that the exposure is interrupted after about four seconds; the buzzer should sound and the Inhibit
indicator should light.

7. Press the key on Service laptop to display the exposure parameters; check that the value for mAs is 600
mAs or less.

Pass Fail

6-3 Minimum Exposure Time

This procedure checks that the minimum exposure time is less than 16 ms.
1. Select a workstation which uses AEC.

2. Select the large focal spot .

3. Use Three Point mode, using values of 150 kVp, maximum mA, and 0.1 s.
4. Set the SID to approximately 1 m (39 inches).
5. Open the collimator.
6. Select each of the three measurement cell in turn. For each one:
- Center the X-ray tube on the chosen measurement cell.
- Make an exposure.

- Press the key on Service laptop to display the exposure parameters; check that the value for
exposure time is less than 16 ms.

Pass Fail

5-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/12 CHK JEDI 38-2

Illustration 1 - JEDI 50Plus R 1T Accuracy - Small focal spot - Radiography - 3 points - Tube:

60 kVp 80 kVp 120 kVp

mA 54.55 Data Data 73.65 Data Data 121.4 Data Data
mA ms mA ms mA ms
65.45 limits limits 86.35 limits limits 138.6 limits limits

20 1000 20 1000 20 1000

15.87 945 15.87 945 15.87 945

20
--- --- --- --- --- --- --- --- ---
24.12 1055 24.12 1055 24.12 1055

50 400 50 400 50 400

43.56 377 43.56 377 43.56 377

50
--- --- --- --- --- --- --- --- ---
56.44 423 56.44 423 56.44 423

100 200 100 200 100 200

88.14 188.18 88.14 188.18 88.14 188.18

100
--- --- --- --- --- --- --- --- ---
111.86 211.82 111.86 211.82 111.86 211.82

160 125 160 125 160 125

140.64 117.31 140.64 117.31 140.64 117.31

*160
--- --- --- --- --- --- --- --- ---
179.36 132.69 179.36 132.69 179.36 132.69

* for 50/65/80 kW only

CAUTION 1- kVp values are measured using kV peakmeter Keithkey 35080A.

2- mA, time and mAs measurements must be made using the post display of Console.

5-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/12 CHK JEDI 38-2

Illustration 2 - JEDI 50Plus R 1T Accuracy - Large focal spot - Radiography - 3 points - Tube:

60 kVp 80 kVp 120 kVp

mA 54.55 Data Data 73.65 Data Data 107.05 Data Data
mA ms mA ms mA ms
65.45 limits limits 86.35 limits limits 123.2 limits limits

20 1000 20 1000 20 1000

15.87 945 15.87 945 15.87 945

20
24.12 1055 24.12 1055 24.12 1055

50 400 50 400 50 400

43.56 377 43.56 377 43.56 377

50
56.44 423 56.44 423 56.44 423

100 200 100 200 100 200

88.14 188.18 88.14 188.18 88.14 188.18

100
111.86 211.82 111.86 211.82 111.86 211.82

200 100 200 100 200 100

177.07 93.68 177.07 93.68 177.07 93.68

200
222.93 106.31 222.93 106.31 222.93 106.31

320 63 320 63 320 63

283.44 59.66 283.44 59.66 283.44 59.66

* 320
For 50/65/80 356.56 68.34 356.56 68.34 356.56 68.34
kW only

500 10 500 10 500 10

396.6 8.63 396.6 8.63 396.6 8.63

** 500
For 65/80 kW 603.4 11.36 603.4 11.36 603.4 11.36
only

630 10 630 10 630 10

502.9 8.63 502.9 8.63 502.9 8.63

*** 630
For 80 kW only 757.14 11.36 757.14 11.36 757.14 11.36

5-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 9/12 CHK JEDI 38-2

Illustration 3 - JEDI 50Plus R 1T Accuracy Small Focal spot - Radiography 2 points - Tube:

mAs 60 kVp 80 kVp 120 kVp

Displays mAs mAs mAs

0.26 0.26 0.26

0.5

0.74 0.74 0.74

18.28 18.28 18.28

20

21.72 21.72 21.72

46 46 46

50

54 54 54

5-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 10/12 CHK JEDI 38-2

Illustration 4 - JEDI 50Plus R 1T Accuracy Large focal spot - Radiography 2 points - tube:

mAs 60 kVp 80 kVp 120 kVp

Displayed mAs mAs mAs

0.26 0.26 0.26

0.5
0.74 0.74 0.74

18.28 18.28 18.28

20
21.72 21.72 21.72

73.72 73.72 73.72

80
86.28 86.28 86.28

5-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 11/12 CHK JEDI 38-2

Illustration 5 - Reproducibility and Linearity of Exposures in 2 points mode - Tube:

70 kVp - 200 ms

20 mAs (100 mA) 25 mAs (125 mA)

mR (R1) mAs (A1) mR (R2) mAs (A2)

10

Rm
Xm
C
(< 0.05)
L
(< 0.1)

Refer to section 5–4 for C and L calculation formula.

Measurement of mAs must be made using the post display of

CAUTION
the Control Console.

5-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 12/12 CHK JEDI 38-2

Illustration 6 - AEC: Reproducibility of Exposures

MODE 2–POINT 3–POINT

kVp =120 kVp = 70

mAs = 20 mA = 250
ms = 1000

DOSE cGy (mR) cGy (mR)

1
2
3
4
5
6
7
8
9
10

Rm

C
(< 0.05)

Refer to section 5–4 for C calculation formula.

5-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 CHK JEDI 38-4

subassembly: Invasive mA Measurement

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

Not applicable.

2 TOOLS

A multimeter and an oscilloscope with a filtering capability.

3 SAFETY PRECAUTIONS

To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

5-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 CHK JEDI 38-4

5 DISASSEMBLY

The Invasive mA Measure can be made on the both side of

the Inverter Unit.

Inverter
Unit

LEFT
ACCESS RIGHT
ACCESS

5-1 Disassembly - Right access

1. Remove the 5.5mm hex head screws which secure -

the right cover of the Power Unit.
Remove the cover.

1
1

5-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 CHK JEDI 38-4

HV Tank KV Measure Board

J6 J2
KV+ measure
HV+ 2

46
sh3 sh4
10 ohms 10 ohms To KV Control Board
1% 1%

3 45

2 1
KV- measure
HV- 1
Measurement tool
(multimeter or
mA= V/(sh3//sh4)= V/5ohms

2. Put a probe inside the generator on the shunt SH3 (right side of the resistor) of KV Measure board on HV
Tank 1 .

3. Connect a second probe on the mechanical ground 2 .

4. Check the resistor value with a multimeter: it should be 5 ohms (+/- 0.05).

5-2 Disassembly - Left access

1. Unscrew the 5.5 mm screws securing the two EMC

cover panels 1 at the HV connections side and
remove them.

1
Take great care not to let screws fall into
NOTICE the HV connector receptacles. Cover
them with plastic caps.

5-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 CHK JEDI 38-4

HV Tank KV Measure Board

J6 J2
KV+ measure
HV+ 2

46
sh3 sh4
10 ohms 10 ohms To KV Control Board
1% 1%

3 45

KV- measure
HV- 1
Measurement tool
(multimeter or
mA= V/(sh3//sh4)= V/5ohms

2. Put a probe inside the generator on the shunt SH3 (right side of the resistor) of KV Measure board on HV
Tank 2 .
3. Connect a second probe on the mechanical ground 3 .
4. Check the resistor value with a multimeter: it should be 5 ohms (+/- 0.05).

6 mA MEASUREMENT
1. Power on the generator
2. Use a multimeter for mA <= 50 mA with a exposure time set to 1s minimum.
3. Use an oscilloscope for other mA, the signal must be filtered at f <= 10 kHz.

5-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

5-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 6 JEDI GENERATOR THEORY AND

FUNCTIONAL DESCRIPTION
SECTION Content Version Page
1 Theory of Operation 0 6-1
2 Theory Presentation 0 6-3

SECTION 1
THEORY OF OPERATION

1-1 GLOSSARY
Glossary of terms used in this document:
Term Definition
ABC Automatic Brightness Control. Regulation loop which makes the measured
brightness equal to brightness demand
AEC Automatic Exposure Control. Exposure cut off technique which uses the
brightness signal to cut the exposure
CAN Controller Area Network. A network used for localized control.
CPU Control Processor Unit. Microprocessor and peripherals which run the
software/firmware
EPLD Erasable Programmable Logic Device.
EMC Electro Magnetic Compatibility. The EMC function prevents the generator
from polluting the power source.
FPGA Field Programmable Gate Array. It is programmed by the CPU core after
the reset and handles all the exposure control logic including the system
interface real–time lines.
HV Ripple High voltage variations due to inverter current pulses. Typically a few
percent.
State Machine Software or hardware function which handles the state of a system and
authorize to go to the next state upon reception of specific events.
IGBT Insulated gate bipolar transistor. A type of power switch
Ilp HV power inverter parallel resonant current; current in the parallel inductor
Ilr HV power inverter serial resonant current; current in the serial inductor.

MOS Metal Oxide Semiconductor. A type of power switch

OGP On Gantry Processor. Unit which drives the generator in CT systems
PDU Power Distribution Unit
RMS Root Mean Square

6-1
 1-2
REV 19
JEDI GENERATOR / FUNCTIONAL ARCHITECTURE

Illustration 1 -
System Control Bus
System Interface
GE MEDICAL SYSTEMS

Low Voltage
heater supply
kV Control Heater Power Rotation
bus
Supply

DC Bus
JEDI HIGH LEVEL BLOCK DIAGRAM

AC/DC

6-2
Jedi Generator / Functional Architecture

rotation phases

High Voltage High Voltage HV Cables

EMC Inverter Tank
Filter

X*Ray Tube 1
1 phase
3 phase power
tube cooling
input
input
DIRECTION 2273022-100
Service Manual
PROTEUS XR/a
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2
THEORY PRESENTATION

2-1 INTRODUCTION

Jedi is the engineering name for a family of compact high frequency X-Ray generators. This generator family
covers a wide range of applications from mobile equipment up to vascular systems:
• JEDI 12-25 kW: Mobile applications
• JEDI 24-48 kW: CT applications
• JEDI 32-50 kW: RAD applications
• JEDI 50-65-80 kW: RF applications
• JEDI 100 kW: VASCULAR applications

2-2 STANDARD FEATURES

Jedi is a family of 150 kV generators operating from 12 kW up to 100 kW for all the major radiological,
fluoroscopic and CT applications. The family handles 1 ms to continuous exposures with tube currents ranging
from 0mA up to 1000 mA.
The generators feature the very latest technology available:
• Constant potential independent of line voltage variations
• Power generation by a high-frequency converter (High voltage ripple: 40 kHz-140 kHz)
• Distributed micro-processor controlled functions (CAN bus)
Other features include:
• Single phase, three phase or battery power source
• Very low kV and mA ripple, excellent accuracies and dose reproducibility
• Compatible with a wide range of tubes, high speed or low speed, can supply up to 3 different tubes. Thermal
load interactive integrator ensuring optimum use of the heat protection curve of the x-ray tube
• Available in various packaging configurations: gantry, under-table, cabinet
• Serviceability: high reliability, fast installation (no generator calibration), application error codes ensure fast
troubleshooting
• Meets CE marking (and in particular EMC), IEC, UL, CSA, MHW regulations (if required)
• Optional pulsed fluoroscopy

6-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-3 APPLICATIONS

RAD Surgery RF Vascular/Car CT

diac
3 Points Mode x x x
2 Points Mode x x x
1 Point Mode x x x
0 Point Mode x x
AEC x x x
Tomography x x
AET x x
Continuous/Pulsed Fluoroscopy x x x
Rad Exposures x
Cinema 30 fr/s x
Cinema 90 fr/s x
ABC x x
Variable mA Scans x
Low mA Fluoroscopy x

Legend:
- AEC - Automatic Exposure Control
- AET - Automatic Tomographic Exposure
- ABC - Automatic Brightness Control in fluoroscopy

6-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-4 ARCHITECTURE

Refer to Illustration 1: Jedi Generator / Functional Architecture

The Jedi family is composed of 3 elements:

2-4-1 A Kernel

• High voltage chain composed of kV control, HV power inverter and HV tank

• Anode rotation function
• Tube filaments heater function
• Control bus for communication between the functions
• DC bus for power distribution to each function
• Input voltage to DC conversion: AC/DC function
• Low voltage power supply
• Application software, running on the kV control board
These functions are the Jedi core. They are present in all versions of the generator.
A function can be unique for all products, or can have several different releases based on product specification.
Examples:
The anode rotation function is available in 2 releases:
• low speed rotation for applications where the tube has a max rotation of 3000 rpm
• high speed/low speed rotation for applications where at least one of the tubes can use
8000-10000 rpm
The control bus is unique.

2-4-2 Options Depending on the Application

• A System Interface which can be:

- CT interface
- RAD interface (console interface, room interface, AEC management present or not)
- ATLAS interface
• EMC function
• Grid function (RF, vascular)
• Bias function (RF, vascular)
• Tube management (2 tubes or 3 tubes option)

6-5
 REV 19
JEDI GENERATOR / FUNCTIONAL ARCHITECTURE

Illustration 2 -
System Control Bus
GE MEDICAL SYSTEMS

System
Interface

heater supply Low Voltage

kV Control Heater Rotation
bus Power
Supply
preload (1 phase)
DC Bus

6-6
AC/DC
Jedi Generator / Functional Architecture

Tube Selection Tube

fil. drives
Management

HV measures

inverter controls
High Voltage High Voltage HV Cables
rotation
rotation

EMC Inverter
+safeties+f

Tank
Filter
+safeties+fans

Grid/Bias X*Ray Tube 1 X*Ray Tube 2 Chiller

1 phase or 1 phase tube
3 phase power cooling
input input
DIRECTION 2273022-100
Service Manual
PROTEUS XR/a
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-4-3 A Packaging Architecture

The packaging architecture consists in a set of boxes which can be put together in several ways to make Jedi fit
either in a cabinet, or a console foot, or a table foot. The boxes can also be split in 2 units distant of several
meters (example: CT gantry). Refer to Illustration 3.
The boxes normally consist of the following:

2-4-3-1 Auxiliaries Box

• Rotation function
• Heater function
• Low voltage power supply (which can also be in the AC/DC box)
This box is always present.

2-4-3-2 Power Box

• HV tank
• HV power inverter
• kV control
• System interface (for the less complex system interface)
This box is always present.

2-4-3-3 AC/DC Box

• MC filter (optional)
• AC/DC function
• Low voltage power supply (which can also be in the auxiliaries box)
This box is always present.

2-4-3-4 System Interface Box

• RAD interface
• AEC interface
This box is present in the RAD product.

2-4-3-5 Optional Boxes

• Tube selection
• Grid/Bias control

6-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 3 - Jedi Generator / Packaging Architecture

Inverter Assembly
Dual Snub LVPS Board
(for TIGER) AC/DC
Tube Board
Gate Command
HV Board
+-

KV Measure HV Tank Rectifier

Block

CT
Inter KV Control Board
face
EMC Filter (Optional)

Power Box AC/DC Box

LVPS Board RAD AEC

(for NP and Interface Interface
Emperor)

Heater Board

System Interface Box

Rotation Board for the rad product

Tube Grid/Bias
Selection Control
Rotation Rotation
Capacitor Capacitor

(optional)
Auxiliaries Box Optional Boxes

6-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 7 EXCEPTION HANDLING AND ERROR

CODES
SECTION 1
TABLE
1-1 Theory of Operation

7-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-1-1 System Operation

The table top floats or rides on eight ball bearing assemblies located inside the
table top area. Each longitudinal bearing assembly consists of precision
machined steel blocks with three (3) bearings bolted to each block assembly
(totaling 12 ball-bearings for longitudinal table travel). Four linear bearings
translate on hardened and polished steel shafts which permit transverse travel of
the table top.

Four electro-magnets (24 VDC) are positioned extremely close to the rails that
the bearings ride on. These magnets “grab” the steel rails securely, locking the
longitudinal travel of the table. Four solenoid-operated fail-safe tilt locks are used
to grab the transverse shafts, locking the transverse travel of the table.
Depressing the four-way float pedal de-energizes the magnets and energizes the
solenoids, allowing the table top to float freely.

The bucky housing assembly rides on four linear ball-bearings mounted to

adjustable brackets attached to either side of the housing. These bearings travel
on the hardened and polished steel shafts of the bucky carriage. One electro-
magnet on the underside of the housing “locks” the bucky into place until the
bucky lock release switch is depressed, thereby releasing the magnet’s hold and
allowing free movement of the bucky.

1-2 Vertical Travel (for Hi-lo Elevating Tables Only)

Vertical table travel is performed by an electric reducer motor and a lead screw
mechanism assembly inside the base.

1-3 Up-Down Motion Limitation (for Hi-lo Elevating Tables Only)

Limitation of travel for the scissor assembly is accomplished by a link connected
to the scissors in such a way as to slide a flag along the Up/Down Limit Board
until the flag breaks the beam in the opto-interrupter (either up or down
depending on direction of travel). The travel range is factory preset to 800mm
table top to floor (upper limit) to 500mm table top to floor (lower limit).

1-4 Anti-collision (for Hi-lo Elevating Tables Only)

Anti-collision function is accomplished by four position switches. When a barrier
stop table top downward motion, table top may produce some degree distortion.
The position switch will work after the detector of position switches detect the
distortion and prohibit the table motion.
1-5 Pedal Operation
1-5-1 Four-Way Tables
These tables have only one foot pedal (four-way float) which operates an opto-
interrupter on the Lock Control Board.

1-5-2 Hi-Lo Elevating (Six-Way) Tables

The foot pedals have sheet metal tabs which ride in the open slot of the opto-
interrupter (one for each pedal) so that when a pedal is depressed, the tab
moves out of the beam of the opto-interrupter. The left four-way release, the Up
pedal and the Down pedal, work on the Limit Board shared with the Up/Down
limit switches. The right four-way release pedal has its own sense board. Both
boards are plugged into the Six-Way Logic Board via plug-in cables.

7-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-6 SIX-WAY (HI-LO ELEVATING) TABLES

The table’s major electrical components include the AC transformer and fuse
block, printed circuit boards, magnetic locks and the associated wiring
harnesses, the motor and the Up-Down Limit Board. It is suggested that you refer
to chapter 10, Schematics, for the corresponding schematic diagram as you
review this section.
1-6-1 Pedal Interface Board
There are two sub-boards:
• Pedal Board No.1
There are five opto-interrupters interfacing with the first lock-pedal, down-pedal,
and up_lim-slider, down_lim-slider, respectively.
J3 and J4 for remote control (Optional), J2 connected to another Pedals I/F Board
No.2, and J1 to Table Logic Control Board.
Jumper X1 is used for removing the Inhibition SW function for all pedals, and
Jumper X2 only for adding the Inhibition SW function to the two Movement
Pedals
• Pedal I/F Board No.2
The opto-interrupter Q1 is for the second lock-pedals.
1-6-2 Table Logic Control Board
J1 is connected to the power supply: J1-1 and J1-2 to +24vdc switching power
supply, and J1-3 and J1-4 to the.
J2 is optional to the Tomo-link subsystem.
J3 and J4 are connected to front Pedal Interface Board and the back Pedal
Interface Board respectively.
J5 is connected to lateral lock-magnets, longitudinal lock-magnets and Bucky
lock-magnet.
J6-1 and J1-2 to the second safety mechanical switch, J6-3~6 to four anti-
collision switches, J6-7 and J6-8 to the Inhibition Switches(the two is located on
the front and back respectively), J6-11~14 to the lens on the Inhibition Switches.
J7 to the contactor &breaker for the AC motor.
• The Double-click Function (can be selected)
U1:A-U2:A, U1:B-U2:B, U5:A-6:A and related circuitry make up three Double-
click Function circuitry, corresponding to the Up, Down and Lock pedals
respectively. The jumper X1 and X2 are used for selection of the Single-click
or/and Double-click Function on the movement pedals and locks pedals
respectively. And the pedal actions have LED indicators.
• The Protection Circuitry
The U11:A used for inhibiting the simultaneity of the UP and Down.
The U11:B used for inhibiting the lock-pedal's activity as in motion.

U7 and its related circuitry form a Time Safety Protection circuitry (12 seconds,
adjustable) for the motor.

U8 and its related circuitry is another Time Safety Protection (1 minute,

adjustable) for the lateral lock-magnets.
• Pedals Inhibition Function(U15:A and its related circuitry)
There are two Pedals Inhibition Switches located on the front and back of the
table respectively, which are non latching, momentary switches with indicator.
The two indicators should always maintain the same status (ON/OFF) whenever
depressing either of the two switch.
• Anti-collision Function
U13:A and its related circuit will this function.
• The Second Safety Switch (U13:B and related circuit)

7-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

• Lock-magnets Driver Circuit

Q1(MTP3055) and its related circuit is used for lateral lock-magnets, and the
+45VDC, diode D13(MBR1035), resistor R25 and capacitor E5(10000uF) build
up a Rapid Circuitry about 100 milliseconds for the lateral magnet’s start-up.

Q2(MTP2955) and its related circuitry is to drive the longitudinal lock-magets.

• Power Supply
1. +24VDC is supplied by a switching power supply with UL and EMC approved
and can be adjustable in the range from 21VDC to 28VDC.
2. +5VDC is supplied by the MAX726 and its related circuitry.
3. +45VDC supplier circuitry consists of the transformer T1, bridge CR2, etc.

7-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2
JEDI EXCEPTION HANDLING
JEDI software performs auto-test at power up and continuously monitors the
correct operation of its functions during application. Any malfunction is stored in
the JEDI error log and reported to the system through a protocol that transports
error code. Errors found can only be reported if the generator is powered on and
live.

2-1 DIAGNOSTICS

There are different levels of diagnostics.

2-1-1 Power-on Diagnostics

At power-up the kV control performs its own initialisation, checks its memory
integrity (checksum of program and NVRAM) and starts the communication with
its peripherals as well as the system. Communication is permanently checked
afterwards. It then initialises the Rotation board and Heater board with their
respective database parameters and loads kV control FPGA.
Eight LEDs (S7..S0) on kV the control board show the software status.
During power-on, the Heater board and the Rotation board CPUs are initialised
and check their memory integrity and hardware. If a problem is encountered, a
PRD error is reported to the kV control.

2-1-2 Live Diagnostics

1. Under application. Faults will be reported through an error code and

associated message. Some are straightforward and convey the root cause. Refer
to the recommended action in the error list.

2. Diagnostics run separately:

• heating function

• rotation function

• inverter gate command diagnostic;

• inverter in short circuit diagnostic;

• no load HV fucntion diagnostics.

3. Manual Diagnostics

Through a troubleshooting guide based on an error message or when the

generator does not reply.

7-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-2 ERROR CODE STRUCTURE

The error code structure described in this chapter applies to JEDI error detection
and logging. The JEDI error log file can be accessed from the system through the
system console or a laptop (JEDI error log upload functionality).
When an error is detected, it is sent to the system and is logged in parallel in the
JEDI error log file. The file contains a maximum of sixty four logs.
Each log shows the following structure:

Simplified Generator Error Error Data associated Number of Date

error code Phase Class Code with the error code occurrences & time

The fields are described in the following paragraphs.

2-2-1 Simplified Error Code Definition

The simplified error code is a grouping of the JEDI error codes. This field gives a
rapid understanding of which part of JEDI is faulty.

Simplified Description
Error Code
30 Tube spits errors
40 Rotation errors
50 Heater errors
60 Exposure errors (HV inverter + mA measure + exposure control
70 Power supply errors (low voltage + DC bus)
80 Hardware errors (internal communications + cables)
90 Application errors (saved RAM + software)
100 External communication errors
110 Thermal errors
10 Rotation warnings (engineering use)
20 Heater warnings (engineering use)
25 LVPS warnings (engineering use)
27 Application warnings (mainly saved RAM battery change)

7-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-2-2 Generator Phase Definition

The generator phase field contains the state of the generator when the error
occurred.

Generator Description
Phase
0 idle: entered in diagnostic mode
1 powered up; waiting for configuration
2 Stand by: configuration completed, waiting for a preparation
3 Preparation in progress: JEDI gets ready to take X-rays
4 Ready for exposures (rotation at speed; filament; HV inverter drive
5 High voltage on
6 Error detected and not yet cleared

2-2-3 Error Class Definition

There are five classes of errors that correspond to different levels of impact to the
system. The class of errors correspond to the seriousness of the error and the
system software will manage operations

Class Description
1 Errors which have no impact on the system operation.
Errors detected in background diagnostics during application. They are referred
as ”Warning” errors, to monitor drifts and used for engineering tracking.
The generator phase remains unchanged.
Errors are stored in the JEDI error log.
2 Errors which are detected by JEDI and that are recoverable automatically without
noticeable effect on the system, such as error related to recovered tube spits.
The generator phase remains unchanged.
Errors which usually occur during exposure.
3 Errors detected by JEDI during exposure. They stop the exposure and revert the
generator into a safe state.
Error will be reset on Exposure Command release. It will require another
Exposure Command to restart the sequence.
The generator phase is set to ”error” until the error is cleared.
4 Errors which are related to any hardware failures, software application or
communication errors.
JEDI will revert to a safe state.
If preparation is in progress, it is stopped.
Errors are cleared either by a reset error action from the system (for system
having a reset error mechanism) or by a prep release or by a new prep command.
The generator phase is set to ”error” until ther error is cleared.
Application cannot work if errors are persistent.
5 These codes may appear when the generator or tube temperature limits are
reached.
The application waits until the thermal information disappears. The error
information is temporary.
The generator phase is set to ”error” until the error is cleared.
7-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-2-4 Error Code Definition

Each error code comprises two fields (which cannot be generated and used
separately);
• the first field describes the JEDI function which is faulty (referred to as the
function code)
• the second field describes the error detected.
Example: error code 0306 means:
• 03: high voltage generation function;
• 06: no kV feedback on anode.
Function Codes List

Function Description
Code
01 Rotation
02 heater
03 High voltage generation
04 mA control
05 Power supplies
06 System interface
07 Software
08 Application
09 Tube control
10 Tube management
11 Grid
12 Bias
13 AEC
14 Hardware

2-2-5 Data Associated with the Error Code

The field ”data associated with the error code” shows detailed information over
the state of the generator when the error occurred.
Examples: rotation high speed acceleration state, small focus preheat, tube
number 1 selected.

2-2-6 Number of Occurrences

The field ”number of occurrences” is used to log the same error occurring several
times consecutively. Instead of filling the error log file with the same error which
has occurred consecutively several times, the first error is logged and
successive errors are recorded through increasing the ”number of occurrences”
field.

2-2-7 Date & Time

The field ”date & time” stores the date and time when the error occurred. This is
the JEDI internal date and time which may be different form the system date and
time. In the case of logging the same error several times, the field indicates the
date and time of the first occurrence.

7-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 3
ERROR CODES, DIAGNOSTICS & TROUBLESHOOTING
3-1 INTRODUCTION
This diagnostics section is to introduce the JEDI generator with the following
information:
Power-On diagnostics LED indication.
List all the potential error codes that can be issued by JEDI Generator.
Provide error code explanation, potential cause and recommended action.
List of diagnostics aids and explanation of diagnostics.
This section also includes the Collimator error codes.

3-2 POWER ON DIAGNOSTICS

Refer to theory of operation for power-on sequence. This paragraph in this
section is to provide meaning of boards’ LED status. The LED display status is
offering useful information at a glance to proceed to error code based
troubleshooting. Whenever in doubt, a simple step is to watch the LED status
display on the kV control board, than the Rotation and Heater.
kV control LED status:
kV control board
- During Power On Diagnostics :
S0..................S7

_ ⊕ ~~........

S0.........................S7

The 8 LED’s (S0...S7) are lit successively in both directions (Scrolling as

indicated by the arrows): the power up diagnostics are completed, kV control
board is up and running.
S0.....................S7
.
.
.
.

One out of two is lit: Application (Flash) problem. Reloaded the APPL. mx file.
- When an application error occurs (Not PRD)




P
P
e.g: No communication
The simplified error code is displayed on the Leds. They blink; when the error is
cleared ( by a return to the standby mode for example ), the 8 LEDs are lit
successively.
Heater board LED status: (See central listing)
After the power on diagnostics, heater board LEDs DS1 and DS2 are lit
successively. Any different status correspond to an abnormal situation. An error
code is logged. Refer to error code description.
Rotation board LED status: (See central listing)
After the power on diagnostics, rotation board LED DS5 is blinking. Any different
status correspond to an abnormal situation. An error code is logged. Refer to
error code description.

7-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-3 ERROR CODE LIST

The error code list and associated short description is presented below.

Jedi generator error codes

simplified Description Error Error Description
error Class Code
code
30 Tube Spits 2 0301H Tube spit (kV+ and kV- dropped)
2 0302H Tube spit (kV+ has dropped)
2 0303H Tube spit (kV- has dropped)
2 0304H Tube spit (kV regulation error)
2 0305H FPGA problem (restarting safety signal)
2 0324H SPITS(data=1:Anode,2:cathode,4:Both,8:kV
regul)

40 Rotation Error 4 0101H No CAN message received within 5 secs

4 0102H Database not correct
4 0103H Rotation current overload
4 0104H Rotation Openload
4 0105H Rotation Phases unbalanced
4 0106H Rotation Phases error
4 0107H Rotation Inverter permanent overcurrent
4 0108H Rotation command error
4 0109H MAINS_DROP has failed
4 0110H PRD error
4 0111H F0 main frequency problem
4 0149H Unknown Rotation error

50 Heater Error 4 0201H No CAN message received within 5 secs

4 0203H Heater inverter permanent overcurrent
4 0204H Filament permanent open circuit
4 0205H Heater Inverter permanent short circuit
4 0206H Filament too high for Pre-heat
4 0207H Filament too high for Boost
4 0208H Filament too high for Heat
4 0209H Heater command error
4 0210H Current under estimated fork
4 0211H Current over estimated fork
4 0212H MAINS_DROP detected
4 0213H PRD error
4 0214H Stay too long in Boost
4 0215H Filament selection error
4 0216H Measured current while inverter OFF
4 0221H Filament Database not correct
0222H
0223H
0224H
4 0248H Unknown Heater error
0249H

7-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

simplified Description Error Error Description

error Class Code
code
60 Exposure 3 0306H No kV Feedback on anode
errors
3 0307H No kV Feedback on cathode
3 0308H No kV Feedback on anode and cathode
3 0309H kV detected during kV diag
3 0310H kV max detected
3 0311H ILP current not OK
3 0312H ILR current not OK
3 0313H ILR max current detected
3 0314H ILR current timeout
3 0316H Spit Max error
3 0317H Spit Ratio error
3 0318H kV did not reach 75% after 20ms
3 0319H kV unbalanced detected
3 0320H FPGA problem (safety signal)
3 0321H Spit retry failed
3 0323H ILP and ILR current not OK
3 0401H No mA feedback
3 0402H mA scale error
2 0403H mA accuracy exceeded 5%
3 0504H Inverter Gate Power Supply failed
3 0801H Exposure backup mAs exceeded
3 0802H Exposure backup time exceeded
3 0803H Exp cmd while gene not ready
3 1411H Time counter error
3 1407H mAs counter error
3 1408H AEC counter error
3 1409H mAs meter saturated
3 1410H FPGA Locked
3 1420H Tomo exposure cut by tomograph instead
generator

70 Power Supply 4 0501H DC bus out of range

errors
4 0503H Inverter Gate Power Supply error
4 0505H Mains power supply has dropped during exposure
4 0506H DC bus 1 phase precharge error
4 0507H DC bus 1 phase discharge error
4 0510H AEC Cell HV supply error
4 0549H Unknown LVPS error
4 0553H Detected +160V too high
4 0557H Detected +160V too low
4 0563H Detected +15V too high
4 0567H Detected +15V too low
4 0573H Detected -15V too strong
4 0577H Detected -15V too weak

7-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

simplified Description Error Error Description

error Class code
code
80 Hardware error 4 0180H Rotor board communication problem
4 0181H Rotor board has reset
4 0280H Heater board communication problem
4 0281H Heater board has reset
4 0321H kV conversion error
4 0322H kV ref ADC / DAC failed
4 0601H RTL error
4 0602H External CAN bus off
4 0902H tube Fan supply error
4 1402H Internal CAN bus off
4 1403H Connectic Fault
4 1404H FPGA configuration problem
4 1405H Tank sensor problem

90 Application 4 0701H Saved RAM checksum pb

errors
4 0702H Software problem
4 0704H Rotor/Heater hold too long

100 Communicatio 4 0603H Debug screen com error

n errors
4 0604H Database download error
4 0605H TAV communication error
4 0606H MPC/Madrid communication error
4 1301H AEC communication error

110 Thermal error 5 0804H Tank Thermal Error

5 0903H Tube exceeded 70degC

120 Manipulation 5 1500H Tomo brightness error

error
5 1501H Exposure switch released during exposure
5 1502H AEC cut off error

10 Rotor Warning 1 0151H CAN Domain command number error

1 0152H CAN Domain request with no transfer init
1 0153H CAN Domain Toggle bit error
1 0154H CAN Domain : less than 2 data to download
1 0155H CAN Domain Abort received & applied
1 0156H Bad index in config upload
1 0157H Tube switch while rotor not off
1 0158H Acceleration cmd while no tube selected
1 0159H Acceleration cmd while database not OK
1 0160H Database download while rotor speeding
1 0161H Acceleration command not OK
1 0162H Rotor acceleration while in error

7-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

simplified Description Error Error Description

error Class Code
code
1 0163H No CAN message received within 4 secs
1 0164H Rotation Inverter overcurrent (< 3 times)
1 0199H Unknown rotation warning

20 Heater Warning 1 0251H Received command is not OK

1 0252H Heater command not OK
1 0253H No CAN message received within 4 secs
1 0254H Heater inverter overcurrent (inverter1) (<3 times)
1 0255H Filament open circuit (inverter1) (<3 times)
1 0256H Heater Inverter short circuit (inverter1) (<3times)
1 0257H Tube switch while filaments not OFF
1 0258H CAN Domain command number error
1 0259H CAN Domain request with no transfer init
1 0260H CAN Domain Toggle bit error
1 0261H CAN Domain : less than 2 data to download
1 0262H CAN Domain Abort received & applied
1 0263H Database download while heater not cut
1 0299H Unknown Heater warning

25 Low Voltage 1 0550H No more warn +160V too low or too gigh
Power supply
Warnings
1 0551H Detected +160V too high
1 0555H Detected +160V too low
1 0560H No more warn +15V too low or too high
1 0561H Detected +15V too high
1 0565H Detected +15V too low
1 0570H No more warn -15V too low or too high
1 0571H Detected -15V too strong
1 0575H Detected -15V too weak
1 0599H Unknown LVPS warning

27 Application 1 1401H Saved RAM power supply limit reached

warnings
1 0703H Watchdog reset has just occurred

Proteus XR/a Collimator error codes

Error Code Description
Z00 RAM D1 error (fatal)
Z01 EEPROM D1 error (fatal)
Z02 CAN error (bus error, error overrun)
Z03 CAN error (receiver overrun)
Z04 No communication with D2
Z05 Calculation error - height
Z06 Calculation error - width
Z10 Stepping error - height leaves
Z11 Stepping error - width leaves
Z14 Limit switch - height leaves
Z15 Limit switch - width leaves

7-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Eclipse Proteus Collimator error codes

Error Code Description Recommended Reactions
Z00 Collimator UIF board error Restart system; if fail again, Change UIF board
Z01 Collimator Control Board error Restart system; if fail again, Change control board
Z02 Collimator Control board error Dismiss the error, check the local connection cable
Z03 Collimator UIF Error Dismiss the error, check the local connection cable
Z04 Collimator local communication error Check the local connection cable, then restart system;
if still fail, change the boards
Z05 Collimator LCD error Change the LCD.
Z06 Collimator Blade out of limit Restart the system.
Z10 Collimator internal error Reset collimator; if fail again, change collimator
Z11 Collimator internal error Reset collimator; if fail again, change collimator
Z14 Collimator Homing Error Reset collimator; if fail again, change collimator

If the lamp cannot be switched on when push the lamp button on front panel, refer to the following trouble
shooting.
1. Open the collimator front cover, assure stable cable connection on J4, J7 and J8 of user interface board.
2. Push ‘lamp’ button to light on lamp. Check the LED indicator status (DS7, DS10, DS13), as shown in following
Figure

Indicator
Error Recommended Reactions
DS13 DS10 DS7
on - - Lamp failure Exchange lamp
off on on UIF board failure Exchange lamp
off off - System lamp power failure Check power supply unit on system side
Exchange UIF board; if failure remains, change whole
off - off UIF board or UIF panel failure
collimator

7-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-4 ERROR REPORTING

For Jedi generator error code, control console only displays the simplified error
code from the Jedi generator.
Whenever a generator error is displayed on the operator console, the Jedi
errorlog upload functionality is available to get more detailed information about
the error.
This function must be performed from the service laptop.
The simplified error code must be used to find the Jedi error code in the Jedi
errorlog file.
Having these two information, look at the Jedi trouble shooting table to find the
FRU to replace.

For Collimator error code, refer to diagnostic section afterwards for potential
cause and recommended action on Page 7-29

7-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-5 WARNING ERRORS

Warning errors are the result of automated and regular background monitoring
for either software events or voltages threshold overtaking.
Those errors are merely for engineering usage and do not indicate any hardware
error failure.
However, as they are logged into the Generator Err_log file, just as the previous
list of error, they are listed here to help error sorting out.
Should too many of them are seen when viewing error log, it is advised to report
them via CQA, since the equipment is still operating.

10 Rotation Warning 0151H CAN Domain command number error

0152H CAN Domain request with no transfer init
0153H CAN Domain Toggle bit error
0154H CAN Domain : less than 2 data to download
0155H CAN Domain Abort received & applied
0156H Bad index in config upload
0157H Tube switch while rotor not off
0158H Acceleration cmd while no tube selected
0159H Acceleration cmd while database not OK
0160H Database download while rotor speeding
0161H Acceleration command not OK
0162H Rotor acceleration while in error
0163H No CAN message received within 4 secs
0164H Rotation Inverter overcurrent (< 3 times)
0199H Unknown rotation warning

20 Heater Warning 0251H Received command is not OK

0252H Heater command not OK
0253H No CAN message received within 4 secs
0254H Heater inverter overcurrent (inverter1) (<3 times)
0255H Filament open circuit (inverter1) (<3 times)
0256H Heater Inverter short circuit (inverter1) (<3times)
0257H Tube switch while filaments not OFF
0258H CAN Domain command number error
0259H CAN Domain request with no transfer init
0260H CAN Domain Toggle bit error
0261H CAN Domain : less than 2 data to download
0262H CAN Domain Abort received & applied
0263H Database download while heater not cut
0299H Unknown heater warning

7-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

25 Low Voltage 0550H No more warn +160V too low or too high
Power Supply
Warnings
0555H Detected +160V too low
0560H No more warn +15V too low or too high
0561H Detected +15V too high
0565H Detected +15V too low
0570H No more warn -15V too low or too high
0571H Detected -15V too strong
0575H Detected -15V too weak
0599H Unknown LVPS warning

27 Application 1401H Saved RAM power supply limit reached

warnings This message is the result of a computation that is
made by the software based on the Date for a
period of approximately 7 years

7-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-6 DIAGNOSTICS
This chapter describes diagnostics tools based on error codes and specific
diagnostics.
BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS
WARNING OFF. APPLY LOCK OUT-TAG OUT PROCEDURE FOR YOUR OWN SAFETY
WHEN MANIPULATING INSIDE THE EQUIPMENT IS REQUIRED.
3-6-1 Detailed Error Description & Troubleshooting Guide
The first part details errors, while the warning errors are listed in a second part of
this chapter.
The table below provides guidelines to troubleshoot Generator and Collimator
problems based on error code.
For each code, there is:
-Associated message and additional explanation related to the error
occurrence.
-List potential cause, in the order of expected probability.
Codes are sorted by ascending order both for simplified code and error code.
Refer to the theory of operation for error code structure for Generator error code.
Information about associated data structure is located at the end of each error
code subset whenever it applies.
Whenever wiring, cabling, LED check is mentioned in the recommended actions,
refer to the central listing.
3-6-1-1 Errors
Tube spits detection Errors (Code 30)

Class 2 Message/explanation Potential cause

Error code
30- Tube spit (kV+ and kV- dropped) x-ray tube spit.
0301H kV drop/spit detected
30- Tube spit (kV+ has dropped) 1. Anode side Tube spit.
0302H kV drop/spit detected on Anode side 2. Anode HV cable
3. HV tank
30- Tube spit (kV- has dropped) 1. Cathode side Tube spit.
0303H kV drop/spit detected on cathode side 2. Cathode HV cable
3. HV tank
30- kV regulation error 1. smooth HV tube spits
0304H This is a slow speed safety circuit in case of 2. kV control board (HV
“smooth” spits. regulation problem)
3. too much line impedance
4. half of AC/DC capacitors
open
5. Inverter (parallel inductor or
filtering capacitors)
6. HV tank
30- Re-starting safety. (unknown reason) 1. External unknown cause.
0305H Error occurring on safety line, while No root error 2. kV control board.
present at the error inputs (Err 0301 to 0304). This
is probably due to transient interference (Spikes).

7-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

30- SPITS(data=1:Anode,2:cathode,4:Both,8:kV 1. Cathode spit if data =1/

0324H regul) anode spit if data=2 ,spits on
both if data =4
Cathode/anode HV cable
2. HV tank
3. IF data=8 run diagnostic for
error 0304H above

Anode Rotation errors (Code 40)

Class 4 Message/explanation Potential cause

Error code
40- No CAN message 1. kV Control main
0101H received within 5 sec’s software lost
The rotation board has not 2. kV control or Rotation
received any signal from board driver failure
the kV control main 3. Bad contact on one of
software for the last 5 sec., the pin on the CAN bus
interpreted as a loss of line connector
communication
40- Database not correct. Wrong kV control Database.
0102H The firmware of the It can only happen at power
rotation board has up.
detected that the
Database received from
the kV control board has
wrong data.
40- Rotation current overload 1. Rotation board
0103H Rotation board has 2. Wrong Database
detected Main or auxiliary (improbable)
rotation current too high
compared to the max.
Tube motor current.
40- Rotation current openload 1. Tube stator winding is
0104H Rotation board detected open circuit: x-ray tube
that no current is flowing to 2. Incorrect wiring (Open)
the motor. 3. No DC bus on Rotation
board
4. Rotation board
40- Rotation phases 1. One rotation wire
0105H unbalanced missing
The amplitude difference 2. Rotation board
of the current between 3. Wrong tube
main and auxiliary is too configuration database
large.
40- Rotation phase error Rotation board
0106H The rotation board has
detected that the current in
the anode stator does not
show the correct phase
shift between main and
auxiliary.

7-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error code Message/explanation Potential cause

40- Rotation Inverter 1. Rotation board
0107H permanent overcurrent 2. Tube stator winding in
An overcurrent has been short circuit -> x-ray tube
detected and 3 restart 3. Wiring incorrect
have been tried (shorted)
unsuccessfully within a
single rotation state
40- Rotation command error. No hardware failure
0108H Rotation board has
informed kV control board
that the command was
erroneous; this is a
DEBUG error.
40- MAINS_DROP has failed 1. Interference (spikes)
0109H The firmware of the 2. Mains drop
rotation board has 3. Cable or connector
detected the mains_drop contact in DC bus
signal activation and between power unit and
transmitted error to kV auxiliary unit
control 4. Rotation board
40- PRD error Rotation board
0110H Firmware checksum, RAM
test and EPLD access are
performed at power up or
reset.
40- F0 main frequency Rotation board
0111H problem.
EPLD has not applied the
inverter start command.
40- Unknown Rotation error. Software problem
0149H The main software
received an error from
rotation board with no
error code associated.
40- Error message from rotor Hardware/Software Conflict
111H firmware

Associated data structure:

PRD error:

component failure:
0001H=RAM
0002H=RAM stack
0200H=EPLD
8000H=program checksum

7-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Rotation database error:

2 bytes data, each value points to a specific parameter found as being erroneous

other errors:
rotation state:
0=inverter OFF
1=acceleration 0 to low speed
2=acceleration 0 to high speed
3=acceleration low speed to high
4=low speed run
5=high speed run
6=high speed to low speed brake
7=brake reverse
8=brake DC

Filament Heater errors (Code 50)

Class 4 Message/explanation Potential cause

Error code
50- No CAN message received within 5 1. kV Control main
0201H sec’s software lost
The Heater board has not received 2. kV control or Heater
any command from the kV control board driver failure
main software for the last 5 sec., 3. Bad contact on one of
interpreted as a loss of the pin on the CAN bus
communication line connector
50- Heater inverter permanent Heater board
0203H overcurrent. (SW limit)
Issued by the heater board when an
overcurrent has been detected and 3
restarts have been tried without
success within 100 ms
50- Filament permanent open circuit. 1. X-ray tube filament open
0204H Issued by the heater board when an 2. Heater to HV tank cable
open has been detected and 3 3. Cathode HV cable or pin
restarts have been tried without contacts
success within 100 ms 4. Open circuit in filament
transformer inside HV
Tank.
50- Heater Inverter permanent short Heater board
0205H circuit (HW limit)
Issued by the heater board when a
short circuit has been detected and 3
restarts have been tried without
success within 100 ms
50- Filament current too high on inverter 1 1. Tube Database or
0206H for “Pre-Heat” calibration
This is the result of an integrated 2. Heater board
value of the RMS current
measurement on Heater board
comparison with max. Tube value in
Database.
7-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error code Message/explanation Potential cause

50- Filament current too high on inverter 1. Tube Database or
0207H 1 for “Boost” calibration
Same as above 2. Heater board
50- Filament current too high on inverter 1. Tube Database or
0208H 1 for “Heat” calibration
Same as above 2. Heater board
50- Heater command error No hardware failure
0209H Heater board has informed kV
control board that the command was
erroneous; this is a DEBUG error.
50- Current under estimated fork/range Heater board
0210H RMS filament current measurement
(every 0.5 msec.) on heater board is
too high
50- Current under estimated fork range 1. Open circuit
0211H RMS filament current measurement 2. Heater board
(every 0.5 msec.) on heater board is
too low
50- MAINS_DROP detected. 1. Interference (spikes)
0212H The firmware of the Heater board 2. Mains drop
has detected the mains_drop signal 3. Cable or connector
activation and has transmitted error contact in DC bus
to kV control between AC/DC and
auxiliary unit
4. Heater board
50- PRD error 1. Heater board
0213H Firmware checksum, RAM test and 2. No -15V on Heater
EPLD access are performed at board
power up or reset.
50- Boost too long on inverter 1. May be a loss of
0214H Boost command stayed longer than communication during
400 ms boost.
50- Filament selection error. Heater board
0215H The relay on the Heater board
selecting the filament is in the wrong
position with respect to the selection
50- Measured current while inverter OFF Heater board
0216H Inverter current has been measured
while the inverter was not
commanded
50- Filament Database not correct Wrong kV control
0221H The firmware of the heater board has Database. It can only
0222H detected that the Received Database happen at power up.
0223H from kV control contains erroneous
0224H data for Tube 1, 2, 3, or 4.
50- Unknown heater error Software problem.
0248H The main software received an error
0249H from heater board with no error code
associated.

7-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Associated data structure:

PRD error:
component failure:
0001H=RAM
0002H=RAM stack
0200H=EPLD
8000H=program checksum

Filament database error:

2 bytes bitmap (LSByte=small focus, MSByte=large focus)
Each bit points to an erroneous parameter
other errors:
1 byte bitmap with the following structure:
bit7 (MSB) bit6 bit5 bit4 bit3 bit2 bit1 bit0 (LSB)
focus selected tube selected small focus state large focus state
0=small focus selected 1=tube 1 selected 0=inverter OFF 0=inverter OFF
1=large focus selected 2=tube 2 1=preheat 1=preheat
3=tube 3 2=boost 2=boost
4=tube 4 3=heat 3=heat
Exposure errors (Code 60)

Class 3 Message/explanation Potential cause

Error code
60- No kV feedback on anode 1. HV cable short circuit
0306H side 2. HV tank
kV measured <12 kV 0,5 ms 3. kV control board (less
after start of exposure on probable)
anode side only
60- No kV feedback on cathode 1. HV cable short circuit
0307H side 2. HV tank
kV measured <12kV 0,5ms 3. kV control board (less
after start of exposure on probable)
cathode side only
60- No kV Feedback (on anode 1. HV tank
0308H and cathode) 2. kV control board
kV measured <12 kV 0,5 ms
after start of exposure on both
anode and cathode.
60- kV detected during kV Improper setup before the
0309H diagnostics. diagnostic is run.
KV measured during inverter
diagnostics while no kV must
be generated.
60- kV MAX detected kV control
0310H kV reached 160 kV during
exposure
60- ILP current not OK. 1. Inverter LC resonant
0311H The current in the parallel circuit (Inverter coil assy,
resonant circuit of the inverter capa inverter assy.)
did not rise at the beginning 2. Inverter
of the exposure. 3. kV control

7-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Class 3 Message/explanation Potential cause

Error code
60- ILR current not OK See above
0312H The current in the serial
resonant circuit of the inverter
did not rise at the beginning
of the exposure.
60- Inverter max. ILR current 1 HV tank
0313H detected. 2 kV control
This is a hardware detection
of maximum current in serial
resonant circuit.
60- ILR Current time out. 1. kV control
0314H The current resonant 2. Inverter
frequency is lower than 3. Current measurement
expected circuit.
60- Spit Max error. Reasonably x-ray tube
0316H kV control has detected the
number of tube spits during
exposure has reached the
limit (see theory of operation,
software section)
60- kV did not reach 75% after 20 kV control
0318H ms.
Indicates that there were no
HV ON signal generated for
exposure time count-up
60- kV unbalanced detected. HV tank
0319H Detects that there is more
than 12 kV difference
between kV+ and kV -
60- FPGA problem; Safety hit 1. This may be due to
0320H with unknown reason transient interference
No error at the inputs while (Spikes).
checking for error source. 2. SW bug
60- Spit retry failed Tube or HV cable
0321H
60- ILP and ILR current not OK 1. Inverter LC resonant
0323H No inverter current measures circuit. (Inverter coil
at the beginning of the assy, capa inverter assy,
exposure cabling)
2. Inverter
3. kV control board
60- No mA feedback 1. HV tank
0401H mA measurement function: 2. kV control board
kV control has detected no 3. x-ray tube (filament
mA feedback 20 ms after the open)
beginning of the exposure.
60- mA scale error 1. kV control board
0402H mA has been measured to be 2. default filament currents
either too low or too high with not correctly adjusted
respect to mA demand 20 ms 3. HV Tank (improbable)
after the beginning of the
exposure

7-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Class 3 Message/explanation Potential cause

Error code
60- mA accuracy exceeded 5% Tube spit
0403H Measured mA every 50 msec
(Class 2 error) exceeded 5% of mA demand.
This error is logged, but does
not stop the exposure.
60- Inverter Gate Power Supply 1. Inverter (gate command
0504H error board)
gate supply voltage has 2. kV control board
dropped below the level 3. Generator input voltage
required to drive the IGBTs too low or line
properly impedance too high
60- Exposure backup mAs 1. Exposure command line
0801H exceeded stuck to the active state
The exposure command last 2. kV control board
so long that the maximum 3. Heater board
mAs allowed has been
reached.
60- Exposure backup time 1. System
0802H exceeded. 2. System-Generator cable
The exposure command last 3. I/F board: exposure line
longer than the duration that stuck to the active state
was loaded by the system
(Backup time + 5%.)
60- Exp cmd while gene not 1. Software bug/problem
0803H ready. 2. Cable / communication
generator received an problem
exposure command while not 3. External cause (Spikes)
in ready state
60- Time counter error. kV control board
1411H Error found in verifying the
counter normal operation.
60- mAs counter error kV control board
1407H Error found in verifying the
counter normal operation.
60- AEC counter error 1. ION chamber
1408H If there is no AEC feedback in 2. AEC cable, connection
AEC station exposure. 3. AEC board
4. kV control
60- mAs meter saturated. kV control
1409H A check is done on mAs
counter operation at the
beginning of exposure and
found the mAs meter with
unrealistic value.
60- FPGA locked. 1. Software problem
1410H FPGA detected an error and 2. kV control
did not allow start exposure
after exposure command
symbol was received
60- Tomo exposure cut by Check the TOMO angle
1420H Tomography

7-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Power supply (Code 70)

Class 4 Message/explanation Potential cause

Error code
70- DC bus out if range (<400 1. mains problem (Too low
0501H or >850) or too high)
2. One phase missing at
Generator input
70- Inverter Gate Power 1. Mains
0503H Supply error (checked at 2. Cable pb
prep) 3. Gate command board
(Inverter)
4. kV control
70- Mains power supply has unknown
0505H dropped During exposure
70- DC Bus 1 phase Not Proteus
506H precharge error
70- DC Bus 1 phase discharge Not Proteus
507H error
70- AEC cell HV supply error Power supply 230Vdc for
510H AEC failed
70- Unknown LVPS error Software problem
0549H The main software
received an LVPS error
with no error code
associated.
70- Detected +160 V too high 1. LVPS
0553H +160 V is higher than 225 2. Heater board
V (measured on heater
board)
70- Detected +160 V too low 1. LVPS
0557H +160 V is lower than 110 2. Heater board
V (measured on heater
board)
Class 4 Message/explanation Potential cause
Error code
70- Detected +15 V too high 1. LVPS open circuit
0563H +15 V is higher than 17.3 2. Heater board
V (measured on heater
board)
70- Detected +15 V too low 1. LVPS open circuit
0567H +15 V is lower than 13 V 2. Heater board
(measured on heater 3. rotation (short circuit)
board) kV control (short circuit)
(improbable)
70- Detected -15 V too high 1. LVPS open circuit
0573H -15 V is lower than -17.3 V 2. Heater board
(measured on heater
board)
70- Detected -15 V too low 1. LVPS (open circuit)
0577H -15 V is higher than -13 V 2. Heater board
(measured on heater 3. rotation (short circuit)
board) 4. kV control (short circuit)
(improbable)

7-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Hardware errors (Code 80)

Class 4 Message/explanation Potential cause

Error code
80- Rotation board 1. Rotation board
0180H communication problem. 2. Control bus cable
kV control board 3. kV control
communication Watch Dog
with Rotation board
popped up because it did
not get reply from Rotation
board.
80- Rotation board has reset. 1. Rotation board
0181H kV control has detected 2. Interference (Spikes)
the Rotation board has
reset. KV control will
reload Rotation Database.
80- Heater board 1. Heater board
0280H communication problem 2. Control bus cable
kV control board 3. kV control
communication Watch Dog
with Heater board popped
up because it did not get
reply from Heater board.
80- KV conversion error KV control board
0321H KV feedback measured
while no KV generated
80- kV ref ADC / DAC failed KV control board
0322H kV control DAC and ADC
capability are permanently
tested for coherency.
80- RTL error (+ associated 1. system communication
0601H data to check which of the power supply (for isolated
4 RTL lines) communications)
Real Time Lines show a 2. system communication
wrong state. RTL’s are cable
tested on a regular basis 3. system interface board
in stand by. 4. system interface to kV
control flat cable
5. kV control board
80- External CAN bus off 1. system communication
0602H power supply (for isolated
communications)
2. system communication
cable
3. system interface board
4. system interface to kV
control flat cable
5. kV control board
80- Tube Fan supply error. 1. No 115 V tube cooling
0902H Rotation board has supply
detected that a wrong 2. Rotation board
voltage is applied to the
tube fan

7-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Class 4 Message/explanation Potential cause

Error code
80- Internal CAN bus off 1. kV control
1402H Can device on kV control 2. Control bus cable
board detected abnormal 3. Heater or Rotation
level on it’s 2 line and sent
error to the CPU
80- Connection Fault Multiple, but likely
1403H One of the flat cable improbable.
connector is not connected
in Generator.
80- FPGA configuration kV control board.
1404H problem.
Detected during power up.
The kV control main
software cannot load the
FPGA.
80- Tank temperature sensor kV control
1405H problem. HV tank
Means that t° value of the
HV tank is < 10°C

Application errors (Code 90)

Class 4 Message/explanation Potential cause

Error code
90- NV RAM checksum pb. 1. Database problem
0701H Generator kV control 2. External cause (Spikes)
board has detected 3. kV control
corruption in the NV Ram
verification (After power
up)
90- Software problem. 1. Software or Database
0702H problem.
2. kV control board failure.
90- Watchdog reset has just 1. Software or Database
0703H occurred. problem.
This error is logged when 2. kV control board failure.
the CPU of the kV control
board is reset by it’s
Watch Dog timer.
90- Rotation/Heater hold too Software problem.
0704H long.
Will pop up if preparation
command from the system
is maintained longer than
3 minutes.
90- Configuration error. Software/hardware conflict.
0705H

7-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Communication errors (code 100)

Class 4 Message/explanation Potential cause

Error code
100- Debug screen com. error Engineering use
0603H
100- Database download error 1. Database file incorrect
0604H Generator has detected a 2. Transmission problem
problem during Database
download
100- TAV communication error. 1. Software / laptop
0605H Generator has detected a problem
communication problem 2. Cable problem
between the I/F and the
service laptop (When
generator is controlled by
the laptop)
100- MPC/Madrid 1. Cable, connection
0606H Communication error. problem between
No reply from the console. Generator and the
(This error message can console.
be seen using the service 2. Interface board
laptop) 3. kV control board
4. Cabling between kV
control board and IF
board
5. Console problem

Not Proteus
100- AEC communication error 1. AEC board
1301H KV Control has detected a 2. I/F board
communication problem 3. kV control
with AEC board. 4. Wiring

Thermal errors (code 110)

Class 5 Message/explanation Potential cause

Error code
110- Tank Thermal Error 1. HV tank too hot; normal
0804H HV tank temperature error
measurement has reached 2. HV tank
60 degree C 3. kV control
110- 70 degree C thermal 1. X-ray tube too hot;
0903H safety error normal error
70° loop detected open 2. Wiring problem
3. Sensor problem (Tube)
4. rotation board

7-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Thermal errors (code 120)

Class 5 Message/explanation Potential cause

Error code
120- Tomo brightness not good Technics (kV,mA) not set at
1500H the correct value. The
brightness signal is out
of range (+/-20%)

120- Exposure switch released Handswitch has been

1501H released before the end
of exposure
120- AEC CUT off error Backup time or mAs too
1502H short; AEC did not cut
the exposure

Proteus XR/a Collimator errors

Error Description Potential cause and recommended action
Code
Z00 RAM D1 error (fatal) Reboot System; If the error still occurs, change D1 board
Z01 EEPROM D1 error (fatal) Reboot System; If the error still occurs, change D1 board
Z02 CAN error (bus error, error overrun) Check CAN cabling (data, voltage) and CAN termination
Z03 CAN error (receiver overrun) Check CAN cabling (data, voltage) and CAN termination
and if heavy traffic on the CAN bus
Z04 No communication with D2 Reboot System; If the error still occurs, change D2 board
Z05 Calculation error - height Reboot System; If the error still occurs, change collimator
Z06 Calculation error - width Reboot System; If the error still occurs, change collimator
Z10 Stepping error - height leaves Observe the error; if it occurs always again in shorter time
intervals, change collimator
Z11 Stepping error - width leaves Observe the error; if it occurs always again in shorter time
intervals, change collimator
Z14 Limit switch - height leaves Reboot System; If the error still occurs, change collimator
Z15 Limit switch - width leaves Reboot System; If the error still occurs, change collimator

Eclipse Proteus Collimator errors

Error Code Description Recommended FE Actions
Z00 Collimator UIF board error Restart system; if fail again, Change UIF board
Z01 Collimator Control Board error Restart system; if fail again, Change control board
Z02 Collimator Control board error Dismiss the error, check the local connection cable
Z03 Collimator UIF Error Dismiss the error, check the local connection cable
Z04 Collimator local communication Check the local connection cable, then restart system; if
error still fail, change the boards
Z05 Collimator LCD error Change the LCD.
Z06 Collimator Blade out of limit Restart the system.
Z10 Collimator internal error Reset collimator; if fail again, change collimator
Z11 Collimator internal error Reset collimator; if fail again, change collimator

Z14 Collimator Homing Error Reset collimator; if fail again, change collimator

7-30
 REV 19
Neon's

*
LEDs

DC bus, 400 ... 800 V

DC bus, 400 ... 800 V Heater Board

*
GE MEDICAL SYSTEMS

DS 1
DS 3

+ M -

1
F

*
INVERTER. & LLC. Circuit DS 1 DC bus, 160V
- 15V
(120 to 200V)
+ 15V
Gate Command Board
DS 300

*
* LVPS

I/F AC/DC NE 1 DS 2
Console PUPT-

7-31
or
DS7-6
DS 1, 2
Illustration1 - GENERATOR Visual Power Supply Distribution

-
- 15 V

+
-15V, +15V DS 3, 2, 1
AEC + 15 V Rotor +5, -15, +15
kV ctrl Board

*
- 15 V "VCC": +5V DS 7
N1 (230 V)
*

+ 15 V

EMC Flt.
3ph, 380 - 480 VAC

CB1
PDU K1
DIRECTION 2273022-100
Service Manual
PROTEUS XR/a
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-7 OTHER FAILURES

Error Message / Potential cause Recommended action Troubleshooting guide

code explanation
System GENERATOR 1. No power on the Perform the troubleshooting in the following way:
does not reply Generator 1/ kV control Leds S0-S7 are lit successively:
to the system 2. EMC filter refer to system communication errors (code
3. AC/DC- Diode bridge 06xx H)
4. Cable between AC/DC
2/ Leds S0-S7 show a specific pattern: refer to
and LVPS
PRD errors section
5. LVPS down
6. CAN cable problem 3/ Led RESET is lit: board is maintained in reset
7. kV control either by the system or by a system I/F failure
8. RAD interface or kV control failure
9. AEC board 4/ Led HALT is lit: replace kV control
10. Rotation board 5/ No Led is lit: verify that +5 V on kV control
11. Heater board board (J6, pin 2).is present. If yes, replace kV
12. Inverter in short circuit control. If no:
13. Generator to system
6/ Verify if +15 V/-15 V is present (Leds
cable
DS1/DS2).
If yes:
Verify that mains_drop line is not stopping the kV
control software (mains_drop active):
6-1/ Check if DS1 LED on LVPS board is lit. If
yes, replace LVPS board.
6-2/ Disconnect Heater board control bus cable.
Check if kV control software starts. If yes,
replace Heater board.
6-3/ Disconnect Rotation board control bus cable
and connect it directly to LVPS board. Check
if kV control software starts. If yes, replace
rotation board.
6-4/ If AEC existing, disconnect AEC cable (J5)
from IF board (J3) cable. Check if kV control
software starts. If yes, disconnect AEC
chambers and connect AEC board to IF
board. If kV control starts, check AEC
chambers, else replace AEC board.
6-5/ Disconnect IF board cable (J10). Check if kV
control software starts. If yes, replace IF
board, else: replace kV control board.
if no:
7/ Verify if +15 V/-15 V is present on rotation
board (DS1/DS2) and the 160 V is present on
the heater board (DS3). If yes: check the
control bus cable to the kV control board. If no
error, change the kV control board. If no:

7-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error Message / Potential cause Recommended action Troubleshooting guide

code explanation
GENERATOR 8/ Verify if the LVPS DC input is right. If no,
does not reply check AC/DC fuse and input line
to the system If yes:
(Cond‘t)
9/ disconnect all output cables from the LVPS
board. Verify the +15 V/-15 V/160 V output. If
right: reconnect each board successively to
find the one stucking the 15V to ground. If
wrong, replace LVPS board

3 phases CB1 1. Short circuit on 1/ Disconnect DC bus cables between AC/DC

breaker trips Generator: and inverter (on AC/DC side)
in PDU or AC - IGBT in short circuit 2/ Check if these cables are in short circuit. If
FUSES blown yes, replace inverter
- ACDC or bridge rectifier in
short circuit if no,
- EMC filter in short circuit 3/ Remove ACDC board
4/ Check between outputs pins then between
inputs of ACDC board. If short circuit, replace
AC/DC FRU
if no:
5/ Check bridge rectifier, between outputs, if yes,
replace ACDC FRU (including rectifier bridge)
if no:
6/ Check bridge rectifier, between inputs, if yes,
replace ACDC FRU (including rectifier bridge)
if no:
7/ Disconnect AC line input from EMC board.
Check EMC for short circuit between phases.
If short circuit, replace EMC board.
Software or 1. After software download: Retry download
Data base - Incorrect or uncompleted
corrupt download
- Checksum problem

7-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-8 HEATING FUNCTION DIAGNOSTICS

Purpose:
The purpose of this test is to drive the heater inverter(s) on both filaments and all
the tubes connected to the Generator in order to identify a faulty heater FRU or a
wrong connection between heater board, HV Tank and tube(s).

Pre-requisites:
• kV control board alive and running: S0-S7 Leds are lit successively or a
combination of them blink
• heater board alive and running: DS1 and DS2 Leds are lit successively
• heater DC supply present: DS3 Led is lit

Test type: No manual interaction

Sequence:
Select the tube to run the test on, start the diagnostic.
The following sequence runs on the small focus and then on the large focus:
• 5 seconds preheat
• 0,4 s boost
• 5 s heat (focal spot max current - 1Amp)
There is 10 s stop time between each focal spot run
During the test, the heater safeties are checked the same way than in application
mode.

Error codes reporting:

Refer to the troubleshooting table.

7-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-9 ROTATION FUNCTION DIAGNOSTICS

Purpose:
The purpose of this test is to drive the rotation inverter(s) in high speed mode (for
application supporting high speed mode) and low speed mode on all the tubes
connected to the Generator in order to identify a faulty rotation FRU or a faulty
dephasing capacitors FRU or a wrong connection between rotation board and
tube.
Pre-requisites:
• kV control board alive and running: S0-S7 Leds are lit successively or a
combination of them blink
• rotation board alive and running: DS5 Led blinking
• rotation DC supply present: DS7 neon is lit
• cabling between rotation board and tube checked
Test type:
No manual interaction, no loop on
Sequence:
Select the tube to run the test on, start the diagnostic.
The following sequence runs in low speed mode and then in high speed mode (if
high speed mode allowed):
• acceleration (time depends on tube type)
• s run
• brake (time depends on tube type)
There is 2 s stop time between each speed mode.
During the test, the rotation safeties are checked the same way than in
application mode.

Error codes reporting:

Error code Associated data Conclusion
0103H Associated data points only to high Power-off. Check if rotation board K2 relay is short
0104H speed mode circuiting the rotor capacitors. If yes replace the rotation
0105H board. If no replace the rotation capacitors
0106H
0103H Associated data points to both high Replace the rotation board
0104H speed and low speed mode
0105H
0106H

For the other error codes, refer to the troubleshooting table.

7-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-10 INVERTER GATE COMMAND DIAGNOSTICS

Purpose:
The purpose of this test is to verify that the HV power inverter drive is working
properly. The IGBTs gate drive supply and the IGBTs gate drive is verified. At the
same time verification is made that no inverter currents nor High voltage are
measured. This test is performed without DC voltage applied to the inverter so
that no Xray is generated. Anode rotation and filament drive are not activated
during this test.
Pre-requisites:
• generator input line in an acceptable range (380V-10% to 480V+10% for 3-
phase AC input)
• kV control board alive and running: S0-S7 Leds are lit successively or a
combination of them blink
• inverter gate_cmd board DC supply present: DS300 neon is lit
Test type: Manual operation is required.
Sequence:
1/ Switch the system OFF. Ensure there is no voltage on AC/DC board
2/ FOR SILHOUETTE VR / PROTEUS XR/a
- Remove DC BUS cable going to Inverter (refer to ”Inverter Power
Assembly” Disassembly/Reassembly procedure)
- Remove the EMC cover (refer to ”Inverter Power Assembly”
Disassembly/Reassembly procedure)
- Refer to Central Listing to ”GATE COMMAND BOARD” and to ”DUAL
SNUB BOARD” or “QUAD SNUB BOARD” for leds location.
3/ Power on the Generator
4/ Verify that the DS1 neon on inverter dual snubbers or quad snubbers board is
not lit
5/ Start the diagnostic and verify:
• error reported on the operator console
• inverter gate_cmd board Leds DS101, DS102, DS201, DS202 are lit: IGBTs
gate drive supply is working properly
6/ Press the exposure switch (10 s exposure is taken after a 10 sec. delay)
7/ During the “exposure”, verify:
• error reported on the operator console
• inverter gate_cmd board Leds DS100 and DS200 are lit: IGBTs gate drive is
working properly
8/ Release the exposure switch
9/ Power off the Generator
10/ Reconnect the 2 DC bus cables from the AC/DC board (see Central Listing).

7-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error reporting:

Error Conclusion
DS1 neon lit Check that DC bus cables have been removed
DS300 neon off Check the gate_cmd supply cable between AC/DC and gate_cmd
board
0301/0302/0303/0304/0309/ Check that DC bus cables have been removed.
0310/0311/0312/0313/0314/ If yes, replace kV control board
0319/0323 (H)
0320 if problem persists, replace Kv control board
0501 kV control or inverter fault, replace inverter first
0503 kV control or inverter fault, replace inverter first
0504 kV control or inverter fault, replace inverter first
one of Replace inverter
DS101/DS102/DS201/DS202
LEDs off while no error
reported
DS100 and/or DS200 LEDs Check cabling between kV control, HV Tank and gate_cmd board.
off If cabling is right, kV control or inverter fault, replace inverter first

7-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-11 INVERTER IN SHORT CIRCUIT DIAGNOSTICS

Purpose:
The purpose of this test is to verify that the HV power inverter is working
properly. The inverter is commanded at a fixed frequency and is loaded with a
short circuit. Verification is made that the inverter currents are correctly set. At
the same time verification is made that no High voltage is measured. This test is
performed without connecting the HV Tank to the inverter so that no Xray is
generated. Anode rotation and filament drive are not activated during this test.
Pre-requisites:
• Generator input line in an acceptable range (380 V-10% to 480 V+10% for 3-
phase AC input)
• kV control board alive and running: S0-S7 Leds are lit successively or a
combination of them blink
• inverter gate_cmd board DC supply present: DS300 neon is lit
• inverter quad snubber board DC supply present: DS1/DS2 neon is lit
• Inverter gate command diagnostic passed without failure
Test type: Manual operation is required.
Sequence:
1. Disconnect the HV Tank primary cables 1 from the inverter (see HV Tank
D/R job card).
Take care not to disconnect at the same time the IGBT middle point 2
Put the short circuit cable 3 (included in the first aid kit) between the two middle
connections as shown:

2. Power on the Generator

3. Verify that the DS1/DS2 neon on inverter quad snubbers board is lit
4. Verify that the DS300 neon on inverter gate_cmd board is lit
5. Start the diagnostic and verify that no error is reported on the operator
console
6. Press the exposure switch (100 ms exposure is taken)
7. Release the exposure switch
8. Verify error reported on the console
9. After exiting the test, power off the Generator
10.Remove the short circuit cable, reconnect the HV Tank primary cables (see
HV Tank or Inverter Power Supply D/R job card). TAKE CARE OF THE
POSITION OF THE TWO CABLES WITH WHITE RINGS.
7-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error reporting:
error Conclusion
DS1/DS2 neon off Check that DC bus cables between AC/DC and inverter
DS300 neon off Check the gate_cmd supply cable between AC/DC and gate_cmd
board
0301/0302/0303/0304/0309/ Check that HV Tank primary cables have been removed.
0310/0319 (H) If yes, replace kV control board
0311 No Ilp current detected. See note 2
0312 No Ilr current detected. See note 3
0313 replace kV control board
0314 Ilr current resonant frequency is lower than expected. See note 4
0320 if problem persists, replace kV control board
0323 Both Ilr and Ilp currents not detected. See note 1
0501 kV control or inverter can be faulty
0503 kV control or inverter can be faulty
0504 kV control or inverter can be faulty
0505 Isolation fault between inverter components and ground. Check inverter
inductors. If no faulty component, kV control or inverter can be faulty
NOTE 1: Ilp and Ilr currents not detected
1. Check the -15 V (Led DS1) on kV control board (see central listing).
If it is not lit, refer to “other failures” section. Else:
2. Power off the Generator. Wait until all neons are off
3. Check that the currents transformers (capacitor set) to gate_cmd board cable
is correctly connected.
If yes:
4. Check that the inverter inductors are correctly connected. If yes:
5. Check that the gate_cmd to HV Tank cable and HV Tank to kV control cables
are correctly connected.
If yes, replace the inverter
6. Reconnect all the cables
NOTE 2: Ilp current not detected
1. Power off the Generator. Wait until all neons are off
2. Check that the parallel inductor is correctly connected. If yes:
3. Check that the parallel inductor impedance is 0 Ohms. If no: replace inverter.
If yes:
4. Check that inverter capacitors (capacitors set) are not broken. If yes, replace
the capacitor set. Else:
5. Disconnect the currents transformers to gate_cmd board cable. Check that
the parallel current transformer impedance is 0. If no: replace the capacitor
set. Else:
6. Check that the gate_cmd to HV Tank cable and HV Tank to kV control cables
are correctly connected. If yes:
7. Disconnect the HV Tank to kV control cable. Check that the impedance
between pin 20 and pin 21 of J2 of HV Tank is 3,3 Ohms. If no replace the
inverter. If yes replace kV control board.
8. Reconnect all the cables.

7-39
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

NOTE 3: Ilr current not detected

1. Power off the Generator. Wait until all neons are off
2. Check that the inductors are correctly connected. If yes:
3. Disconnect the currents transformers to gate_cmd board cable. Check that
the serial current transformer impedance is 0. If no: change capacitor set.
Else:
4. Check that inverter capacitors (capacitors set) are not broken. If yes, replace
the capacitor set. Else:
5. Check that the gate_cmd to HV Tank cable and HV Tank to kV control cables
are correctly connected. If yes:
6. Disconnect the HV Tank to kV control cable. Check that the impedance
between pin 20 and pin 21 of J2 of HV Tank is 5 Ohms. If no replace iverter. If
yes replace kV control board.
7. Reconnect all the cables

NOTE 4: Ilr current resonant frequency is lower than expected

1. Power off the Generator. Wait until all neons are off
2. Check that the inductors are correctly connected. If yes:
3. Check that the inverter capacitors (capacitors set) are not broken. If yes:
replace the capacitor set. Else:
4. Disconnect the currents transformers to gate_cmd board cable. Check that
the parallel current transformer impedance is 0. If no: change the capacitor
set. Else: replace kV control board.
5. Reconnect all the cables

7-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-12 NO LOAD HV DIAGNOSTICS

Purpose:
The purpose of this test is to verify that the HV power inverter and HV tank are
working properly. The exposure is taken as in application mode except that no
filament drive nor anode rotation is running. Verification is made that the inverter
currents are correctly set and that kV regulation is operating properly. As no
filament drive is applied, no X-Ray are generated.
This test also allow to separate Generator from HV cable and x-ray tube problem
by running it without the HV cables plugged on the HV tank (*).
(*) HV Receptacles must be filled with oil before starting test.
Pre-requisites:
• Generator input line in an acceptable range (380 V -10% to 480 V +10% for
3-phase AC input)
• kV control board alive and running: S0-S7 Leds are lit successively or a
combination of them blink
• inverter gate_cmd board DC supply present: DS300 neon is lit
• inverter quad snubber board DC supply present: DS1/DS2 neon is lit
• Inverter gate command diagnostic passed without failure
• Inverter in short circuit diagnostic passed without failure.
Test type: Manual operation is required.
Sequence:
1. Power on the Generator
2. Start the diagnostic and verify:
- error reported on the operator console
- inverter gate_cmd board Leds DS101, DS102, DS201, DS202 are lit:
IGBTs gate drive supply is working properly
3. Select kV (default = 80 kV) and exposure time (default = 1 sec.).
4. Press the exposure switch
5. During the “exposure”, verify:
- error reported on the operator console
6. Release the exposure switch
7. Power off the Generator
Error reporting:
See Troubleshooting Table.

7-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-13 AEC DIAGNOSTICS

Purpose:
The purpose of this test is to drive the AEC function in order to identify a faulty
AEC, IF or kV control board FRU or the wrong connection between the AEC
board and ion chambers.

Pre-requisites:
• application mode without AEC mode is running properly
• kV Control board alive and running: S0-S7 LEDs are lit successively or a
combination of them blink
• cabling between IF board, AEC board and ionization chambers checked.

Test type:
Automated, with the use of Service Laptop

Sequence:
Select AEC function in menu 1 on Service Laptop.
Press V to run the test.
AEC function is verified through a series of 7 tests as follows:
• AEC return measurement test:
A voltage reference is switched to one input of the AEC select multiplex.
Nominal value of return voltage = 5.24 V
Test 1 is OK if: 4 V < measured value < 6 V
This test is also performed at lower frequency count up:
Test 2 is OK if: 4 V < measured value < 6 V.
• Switching Gain test (x10):
A voltage reference is switched to one input of the AEC select multiplex and
count up gain is applied.
Nominal value of return volatge = 4.76 V
Test 3 is OK if: 4 V < measured value < 6 V.
• AEC ion chamber HV power supply test:
A portion of HV power supply is switched to one input of the AEC select
multiplex:
- No cell selected, Test 4 is OK if return voltage measurement is 0 V.
- Select respectively one of the three cells, left, right, middle.
Test 5, 6, 7 are OK if: 1 V < measured value < 3 V.

7-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Error codes reporting:

Error Code Associated Data Conclusion

1111111 (*) None Test OK
Any combination None Test KO = test failed; replace AEC
board
0001000 None Communication error:
- Replace AEC board
- If same problem, apart from a DOA
board, suspect IF board then KV
Control board.

(*) except for AEC board with serial number: 2184569-X: the resulting error code
must be 0001111 (test is OK on this board the HV power supply test is not
performed).
For the other error codes, refer to the troubleshooting table.

7-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank

7-44
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 8 PLANNED MAINTENANCE

SECTION 1
PREVENTIVE MAINTENANCE ACTION LIST
The Proteus System does not require any Planned Maintenance activities for the first 13 months after system
installation.
The following table lists the required planned maintenance activities and the associated Job Card for each task.

Note: The planned maintenance to the OTS suspension see Direction 2277285-100, OTS Suspension
Service Manual.

OPERATION FREQUENCY JOB DESCRIPTION

CARD
GENERAL
General cleaning and As required PM001 Keep all surfaces clean and touch-up paint chips
painting
Visual inspection 12 months PM002 Check for debris that would indicate abnormal wear
Functional checks 12 months PM003 Perform the tasks described in Chapter 4,
Functional Checks
TABLE BASE
Control pedals and 12 months PM004 Check condition and functioning; ensure pedals
movement inhibition buttons and buttons have free play without any obstruction
Emergency buttons 12 months Check condition and functioning; ensure buttons
have free play without any obstruction
Electrical cables 12 months Check condition of cable sheathing and correct
routing
Power and ground 12 months Check condition and connections
connections
Connector panel and cable 12 months Check condition and connections
connectors
Replace lubricant box 12 months Replace lubricant box
Check the lateral lock 12 months Check whether the floating table can be pushed
laterally when it’s locked
PATIENT SUPPORT
Surface finish 12 months PM005 Check condition and clean
Longitudinal bearings 12 months Check condition and lubricate with grease
Longitudinal bearing tracks 12 months Clean and wipe with light machine oil
and rails
Transversal rods and 12 months Check condition; clean and wipe with light machine
bearings oil and lubricate with grease
Rubber bumper end stops 12 months Check condition of stops and tightness of anchoring
(Longitudinal & transversal)
CASSETTE TRAY AND CARRIAGE
Electrical connector and 12 months PM006 Ensure connector is in good condition and making
cable good contact; check condition of cable sheathing
Cassette handle assembly, 12 months Ensure handle and push button have free play
push button & band holder without any obstruction
Bearings and tracks (front 12 months Check condition; clean and wipe with light machine
and rear) oil and lubricate with grease
Rubber bumper end stops 12 months Check condition of stops and tightness of anchoring
Tray 12 months Check general condition of tray
Cassette size marker and 12 months Check condition; clean and wipe with light machine
locking assembly oil

8-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
OPERATION FREQUENCY JOB DESCRIPTION
CARD
ACCESSORIES
Compression band 12 months PM007 Check condition
Patient hand grips 12 months Check condition
GENERATOR
Check generator functions 12 months PM008 Test exposure, including AEC if resent
Record last error codes
Record result on counters
Check technique factors
Tighten terminals and remove dust
Replace NonVolatile RAM Every 8 Years PM Jedi 1. Upload database
on the kV Control Board 15-2 2. Battery replacement
3. Download database
WALL STAND (GPCP NO. 2260354) (OPTIONAL COMPONENT)
General cleaning and As required PM001 Keep all surfaces clean and touch-up paint chips
painting
Visual inspection 12 months PM002 Check for debris that would indicate abnormal wear
Functional checks 12 months PM003 Perform the tasks described in Chapter 5,
Functional Checks
Steel cables 12 months PM009 Inspect and grease length of steel cables; replace if
worn out
Carriage roller bearing 12 months Clean roller bearings and tracks
inspection
Vertical lock 12 months Clean and inspect
LAT bar 12 months Replace grease between the flanges
SG100 WALL STAND (GPCP NO. 2225849) (OPTIONAL COMPONENT)
General cleaning and As required PM001 Keep all surfaces clean and touch-up paint chips
painting
Visual inspection 12 months PM002 Check for debris that would indicate abnormal wear
Functional checks 12 months PM003 Perform the tasks described in Chapter 5,
Functional Checks
Steel cables 12 months PM010 Inspect and grease length of steel cables; replace if
worn out
Carriage roller bearing 12 months Clean roller bearings and tracks
inspection
Counterweight Chain 12 months Inspect and grease length of chains. Replace if
Maintenance excessively worn or rusty.
Vertical lock 12 months Clean and inspect
Angulation Components 12 months Inspect and Replace if necessary
(lock & cable)
Bucky Rotation Lock Check 12 months Verify lock mechanism does not move

Electrical Checks 12 months Inspect and replace any damaged cables or

connectors.
Check grounding.
SG120 WALL STAND (GPCP NO. 2402562) (OPTIONAL COMPONENT)
General cleaning and As required PM001 Keep all surfaces clean and touch-up paint chips
painting
Visual inspection 18 months PM002 Check for debris that would indicate abnormal wear
Functional Checks 18 months Perform tasks described in Chapter 5,
Functional Checks
Carriage roller bearing 18 months PM011 Clean roller bearings and tracks
inspection
Counterweight Chain 18 months Inspect and grease length of chains. Replace if
Maintenance excessively worn or rusty.
Vertical lock 18 months Clean and inspect

8-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
OPERATION FREQUENCY JOB DESCRIPTION
CARD
Electrical Checks 12 months Inspect and replace any damaged cables or
connectors.
Check grounding.
JEDI PREVENTIVE
MAINTENANCE
Replace Nonvolatile RAM Every 8 Years 1. Upload database
on the kV Control board 2. Battery replacement
3. Download database
COLLIMATOR
Check the collimator 12 months PM012 1. Check the flange.
mounting screws 2. If the collimator mounting screws are loose,
apply LOCTITE onto the screws.
X-RAY TUBE CABLES
CHECK
Check the fixing and 12 months PM013 1. Check the fixing and intactness of Anode
intactness of Anode Rotation cable and Thermal Protection
Rotation cable and Thermal cable.
Protection cable 2. Check the stator cable strain relief.

8-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
SECTION 2
PREVENTIVE MAINTENANCE JOB CARDS
The following pages list the preventive maintenance Job Card detailed activities.

PROTEUS XR/a 1/1 PM 001

subassembly: General Cleaning and Painting

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

Cleaning Liquids and compounds.

Touch-up paint.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1)Remove power from the system.

2)Carefully clean all surfaces of the system. Note any paint damage as you clean the system.
3)Apply touch-up paint to any paint-damage areas.
4)Reapply power to the system.

8-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 PM 002

subassembly: Visual Inspection

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1)Remove power from the system.

2)Visually check around the moving part of the system for any debris, wear or damage. This includes the table
top, table base, and wall stand if present.
3)If any debris, wear of damage is observed, replace or repair the affected areas.
4)Reapply power to the system.

8-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 PM 003

subassembly: Functional Checks

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 50 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

No specific precautions.

PREREQUISITES

None.

PROCEDURE

Follow the functional checks specified in Chapter 5 of this Service Manual.

8-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 PM 004

subassembly: Table Base Maintenance

purpose: Maintenance Procedure version no. 3
date: 10/10/06
NF No. Production date Serial No. Personnel:1
from / / from Time: 45 min
to / / to

SUPPLIES

Lubricant.

TOOLS

Measure tape, Oil-proofed gloves.

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

During the maintenances, before removing the motor from under the table, or untie the
CAUTION motor chain, to avoid the injury by the potential dropping table, put the blocks kit
(5137108) over the rod.

1)Control Pedals and Movement Inhibition Buttons.

a) Confirm the control pedals can move up/down when double press and hold the corresponding pedal.
Adjust the locks as required if there is inappropriate table motion.
b) Confirm the table top control pedal unlocks the table top when depressed and locks the table top when
released. Adjust the locks as required if there is inappropriate table motion.
c) Confirm the inhibition button locks table motion when depressed and unlocks when released. Check the
circuit if there is inappropriate motion.

2)Emergency buttons
a) Confirm emergency button removes table power when depressed and applies table power when
released.

3)Electrical cables.
a) Remove power from system.
b) Check condition of all cables including cable sheathing, connectors and overall condition; if any cable
damage is noted, replace or repair affected cable.
c) Confirm that the cable is correctly routed.
8-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 PM 004

4)Power and ground cables.

a) Check that power is removed from system.
b) Check condition of all power and ground cables including cable sheathing, connectors and overall
condition; if any cable damage is noted, replace or repair affected cable.
c) Confirm that the cable is correctly routed.

5)Connector panel and cable connectors.

a) Check that power is removed from system.
b) Check condition of all power and ground cables including cable sheathing, connectors and overall
condition; if any cable damage is noted, replace or repair affected cable.
c) Confirm that the cable is correctly routed.
d) Reapply power when complete.

6)Table height limitation check.

a) Power on the table base.
b) Double step and hold the DOWN pedal until the table motion stop automatically and confirm the table
height is 500mm.
c) Double step and hold the UP pedal until the table motion stop automatically and confirm the table height
is 800mm.

7)Replace lubricant box.

a) Raise the table base to its highest position.
b) Remove the table base cover.
c) Demount the two lubricant boxes.
d) Take off the blocks from new lubricant boxes.
e) Put two new lubricant boxes on.

Note: Lubricant box contains grease lubricant (Part No.

096-0020) inside, pls wear oil-proofed gloves
during replacement, Refer to Materal Safty Data
Sheet (MSDS) file attached for grease lubricant
info.

8)Check bearing and shaft.

a) Use a soft cloth to clean the lubricant oil on the surface of the shaft.
b) Use a soft cloth to clean the lubricant oil on the groove of bearing assembly and bushing.

9)Check lateral lock.

a) Power up the system.
b) Raise the table to its highest position.
c) Power off the system.
d) Remove the carbon fiber plate of the table top.
e) Remove the two screws fastening rod end support.

8-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 PM 004

f) Remove the rod end support.

Note: Do one side at a time.

g) Pull out the supporting rod.

A. Hold the brake plates at release position with ty-raps.
B. FE, on the opposite side, pulls the corner of the table frame which has been removed rod end
support.

C. When the rod is pulled out of rod end support, take out the rod.

8-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
PROTEUS XR/a 4/4 PM 004

h) Remove the old brake plates and replace them with new ones (renewal part number is 612-3440).

i) Use a soft cloth to clean the lubricant oil on the surface of a new rod (renewal part number is 613-3003)
j) Use a soft cloth to clean the lubricant oil in the groove of the two bearings on each side.
k) Insert the new rod.

l) Adjust the screws to make sure the plate travel distance is between 3-5mm, and lock it with locking nut.

m) Repeat the similar steps from e to l as above, to replace the rod and couple of brake plates on the other
end of the table.

8-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 PM 005

subassembly: Patient Support Maintenance

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 45 min
to / / to

SUPPLIES

Grease.
Light Machine Oil.

TOOLS

None.

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

8-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 PM 005

PROCEDURE

1)Surface finish
Remove the dust from the table top and table topside rails.

2)Longitudinal bearings
Remove the dust.

3)Longitudinal bearing tracks and rails

Remove the dust from the bearing tracks and rails. Add the light machine oil on the tracks and rails.

4)Transversal rods and bearings

Remove the dust.

5)Rubber bumper end stops (longitudinal and transversal)

Verify the bumper stops have no cracks and one fixed tightly.

8-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/2 PM 006

subassembly: Cassette Tray and Carriage Maintenance

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 45 min
to / / to

SUPPLIES

Grease.
Light Machine Oil.

TOOLS

None.

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

8-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 PM 006

PROCEDURE

1)Electrical connector and cable

Confirm properly connected.

2)Cassette handle assembly, push button and hand holder

Check the push button function. Check the movement with the handle functions.

3)Bearings and tracks(front and rear)

Remove the dust and add grease or light machine oil.

4)Rubber bumper and stops

Confirm the bumper and stops have no cracks and one fixed tightly.

5)Rubber bumper end stops (longitudinal and transversal)

Verify the bumper stops have no cracks and one fixed tightly.

6)Tray
Confirm the pull-in and pull-out movement is smooth.

7)Cassette size marker and locking assembly

Check the cassette size marker is firmly set and the cassette locking assembly is functional.

8-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 PM 007

subassembly: Accessories Maintenance

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None.

SAFETY PRECAUTIONS

None specific precautions.

PREREQUISITES

None.

PROCEDURE

1)Compression band
Mount and remove the compression band on the table top.

2)Hand grip
Mount and remove the hand grip on the table top.

8-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 PM 008

subassembly: Generator Functional Checks

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 60 min
to / / to

SUPPLIES

Film.
Error–code recording form.
X–ray counter recording form.

TOOLS
Laptop.

SAFETY PRECAUTIONS
No specific precautions.

PREREQUISITES

8-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 PM 008

ÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁ
ÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁ

PROCEDURE

1.1 Test exposure

Technique factors (mA, mAs and ms) are displayed after exposure on the console.

1.2 mA accuracy
Run the exposures in table below and check if the mA value on console after exposure is between the min
and max value.
If not , run the same exposure 10 times with exposure time set to 12.5s and then check again.

1.3 AEC functionality check (if existing)

Put 15cm of Plexiglas or a plastic bucket with 15 cm of water on the table top
Select Two point mode (mAs)
Set kV to 80 kV and mAs to 600
Run the exposure
Develop the film
Check that the density is 1 +/–10%.If not redo AEC calibration. (See Job card in chapter 3)

8-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 PM 008

ÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁÁ

2. Record last error codes

Go to calibration mode by using keys “ALT and S”
Go to MENU 2 with arrow keys
Press (F3) to select LIST
Press (F5) to select the first error code
Fill the chart below with the error code number
Then use F5 key for following error code.
Simplified Error Generator Error Class Data associated with the Number of oc- Date and
Error Code Code Phase Error Code currences Time
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
Refer to diagnostic section (Chapter 7) for fix error (if necessary).
Clear the Error Log after checking. (Use CTRL and H keys, then confirm with W key).

8-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 PM 008

3. Record results on counters

Go to calibration mode by using keys “ALT and S”
Go to MENU 2 with arrow keys
Press (F5) to select NEXP(Number of EXPosures)
Press (F5) to select the first counter
Fill the chart below with the counter number

4. Check technique factors

Run the Accuracy checks in “Functional Check procedure” in Chapter 4.
Make a copy of illustrations 3, 4, 5, and 6 and fill it with the results you get.
5. Tighten terminals and remove dust
– Tighten the inputs connections on generator , located near the labels on AC/DC module (refer to
illustration in disassembly / reassembly section).
– Tighten the DC bus connections on generator located on the upper side of the generator (refer to
illustration in disassembly / reassembly section).
– Verify if all connectors are correctly plugged in.
– Remove dust by using a vacuum-cleaner.

8-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
PROTEUS XR/a 1/2 PM JEDI 15-2

subassembly: Replace Generator Non Volatile Parameters RAM

purpose: Maintenance Procedure version no. 0
date: 21/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 45 min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that the power is off.
To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

Upload the database that is stored in the RAM before starting the replacement procedure (refer to Job Card CAL
JEDI 8-6 ”Backup & Restore Database Setup Parameters”).

8-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/2 PM JEDI 15-2

5 PROCEDURE

5-1 Remove and Replace the RAM

On the kV Control board, note the direction that the RAM faces. Insert the tip of a small screw driver underneath
left side of U32 and lever gently, then grasp it between your thumb and forefinger and pull it directly away from its
support on the board.
Insert the new Nonvolatile Parameters RAM in its place. Be careful to insert it facing in the same direction.

Refer to Central Listing section for more details.

This NV RAM contains a LITHIUM CARBON MonoFlouride (LiCFx) battery, used to

CAUTION provide the battery backup for the static RAM and the time keeper device. Electrical
Characteristics: 3 V - 49 mAh type BR 1225.Resend the former component to your local
GEMS representative for recycling.

5-2 Download Database

Reapply power.
Download the database (refer to Job Card CAL JEDI 8-6 ”Backup & Restore Database Setup Parameters” in
Chapter 4).

8-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
PROTEUS XR/a 1/1 PM 009

subassembly: Wall Stand

purpose: Maintenance Procedure version no. 0
date: 05/04/01
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1) Remove power from the system.

2) Inspect steel cables; replace if worn out.
3) Clean carriage roller bearings and tracks.
4) Clean and inspect the vertical lock.

8-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
PROTEUS XR/a 1/1 PM 010

subassembly: SG100 Wall Stand

purpose: Maintenance Procedure version no. 0
date: 05/04/01
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1) Remove power from the system.

2) Inspect steel cables; replace if worn out.
3) Clean carriage roller bearings and tracks.
4) Clean and inspect the vertical lock.
5) Counter Weight Chain Maintenance.
6) Inspect Angulation Components (lock &cable).
7) Check Bucky Rotation Lock.
8) Electrical Checks.

Note: The procedures in this Job Card are concerted with the revision 6 of SG 100 Wall Stand Service
Manual (GPCP Number 2150297-100). For the reason of the update and change in that manual, it is
recommended to see also the latest Service Manual of SG 100 Wall Stand for reference.

8-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
PROTEUS XR/a 1/1 PM 011

subassembly: SG120 Wall Stand

purpose: Maintenance Procedure version no. 0
date: 30/09/04
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1) Remove power from the system.

2) Clean carriage roller bearings and tracks.
3) Clean and inspect the vertical lock.
4) Counter Weight Chain Maintenance.
5) Electrical Checks.

8-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 PM 012

subassembly: Collimator
purpose: Maintenance Procedure version no. 0
date: 27/09/01
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

Allen Key
Calliper

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

Eclipse
PREREQUISITES Proteus
Collimator
None. Flange

PROCEDURE

1) Remove power from the system.

2) Turn the tube over, and then demount the
collimator. Proteus
XR/a
For MX100 X-ray tube, skip without performing Collimator
step 3)
Flange
3) Check the mounting flange. If wear on the
flange is found (the thickness of the flange
edge is below 1.5mm), the flange should
be replaced with a new one. Ordering
information please refer to Chapter 9.

For Proteus XR/a Collimator, follow 4) and 5).

For Eclipse Proteus Collimator, skip to 6) directly.

4) Check the collimator mounting screws. If

they are loose, please follow the Job Card
IST015 or IST017 for MX100 X-ray tube in
Chapter 2 to apply LOCTITE onto the
screws.
5) Follow the Job Card IST015 or IST017 for
MX100 X-ray tube in Chapter 2 to securely
mount the collimator.

8-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/1 PM 013

subassembly: X-ray tube cables

purpose: Maintenance Procedure version no. 1
date: 12/12/05
NF No. Production date Serial No. Personnel:1
from / / from Time: 15 min
to / / to

SUPPLIES

None.

TOOLS

None

SAFETY PRECAUTIONS

Remove power from the system before beginning work.

Check that power is off.

PREREQUISITES

None.

PROCEDURE

1) Remove power from the system.

2) Check the fixing and intactness of Anode Rotation cable and Thermal Protection cable.
3) Check the stator cable strain relief marked in the illustration for RAD 14,21 X-ray tube.
4) Check the intactness of heat shrink tube, check the fastness of cable clamp and copper strap for RAD 14,
21 tube.
Note: Step 3) is only for RAD 14, 21 X-ray tube, not for MX100 X-ray tube.

Figure 1: RAD 14 X-ray Tube Figure 2: RAD 21 X-ray Tube

Cable strap 3x M4
Cable Clamp screws.

1xM4 screw,
2xM4 flat washers.
Thermal cable Apply Loctite
242(46-170686P1)

clamp
mounting
block
Stator cable
Attach P-clamp
Copper strap
using M4 hex. nut

8-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 9 RENEWAL PARTS

SECTION 1
PROTEUS XR/a SYSTEM RENEWAL PARTS LIST (Not include Jedi Generator)
FOR CONTINUED PROTECTION AGAINST RISK OF FIRE, REPLACE ONLY WITH
WARNING THE SAME TYPE AND RATING OF FUSE.

Item # FRU GPCP NO. Description Quan.

Level
Table
1 2 2259298-14 Table top longitudinal move wheel 2
2 1 2226325-34 Table top bearing 4
3 2 612-3100 Table Top Frame Assy 1
4 1 2259298-31 Table top bearing 4
5 1 2259298-5 EM lock 4
6 1 2259298-23 Micro-movement anti-collision switch 4
7 1 2259298-30 Table top bearing 6
8 1 2259298-6 EM lock 4
9 1 2259298-9 Table elevating motor chain 1
11 1 2338145 (Localized) Cassette Tray-Size Sensing 1
12 2 46-286129p22 Fixed grid (12:1 100cm 60l/cm) 1
13 2 46-286129p1 Bucky grid (12:1 100cm 36l/cm) 1
14 2 2259298-15 Bucky movement bearing 4
15 1 2252611-3 Ion chamber 1
16 1 2259298-71 Table bucky handle 1
17 1 2259298-22 Bucky-lock button 1
18 2 2288705 Bucky handle 1
19 2 2288706 Bucky handle button 1
20 1 2259298-19 Safety button 2
21 1 2259298-27 Table height measure potentiometer 1
22 1 2259298-24 Pedal I/F board assy 1
23 1 2259298-25 Limit I/F board assy 1
24 1 2259298-18 Switch power supply 24VDC 6.5A 1
25 1 2259298-17 AC contactor 240VAC, 2.5kW 1
26 1 2259298-16 Transformer 220AC/30VDC 50W 1
27 1 2259298-26 Table logic control board assy 1
28 1 2259298-7 Table elevating motor 1
29 2 2364950 Table top 1
30 2 2259298-70 Table side cover 2
31 1 2259298-74 Back side foot pedal (set) 1
32 2 2259298-69 Table front & back cover 2

9-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
33 2 5189687 Table end cap assembly with screw (pair) 1
34 1 2259298-67 Bucky EM lock 1
35 1 2259298-68 Bucky power fuse 250V 160mA 2
36 2 2259298-10 Table up/down spring 6
37 1 2348721 Lubricant box 1
38 1 2189553 Table Bucky (LH) 1
39 1 2362889 Bucky Bar Assembly 1
40 1 2259298-4 Front side foot pedal (set) 1
42 2 2259298-11 Table spring 2
43 1 2259298-12 Table top bumper 2
44 1 2259298-20 Inhibition button 2
45 2 2260192 Hand grip (pair) 1
46 1 612-3440 Lateral table lock plate assembly 4
47 2 611-3610 Table bottom front & back cover 2
48 2 611-3601 Table bottom side cover 2
49 1 2259298-21 Emergency stop switch 2
50 1 610-3100 Emergence OFF Switch Assy 2
51 1 2357655 Long sliding ribbon 2
52 1 2357656 Short sliding ribbon 2
53 1 2336280 Spring leaf 2
54 1 2399762 Paint Kit 1
55 1 612-3408 Brake Vane 1
56 1 613-3400 Camera Bracket Assembly 1
57 1 613-3003 Linear bearing shaft 1
58 1 2284482 Condor table relay assembly 1
59 1 5137108 Table Brake Block 1
60 1 5159516-1 Reciprocating Bucky L/H 1
61 1 5159516-2 Reciprocating Bucky R/H 1
62 1 5166100 Step Motor 1
63 1 5166198 Circuit Board L/H 1
64 1 5166059 Circuit Board R/H 1
65 1 5166209 Rail Kit 1
66 1 5166188 250VAC, 315mA Fuse 1
67 1 5166307 250VAC, 160mA Fuse 1
68 1 5167409 AID Ion Chamber 1
69 1 5167409-2 AID Ion Chamber with 24 meter cable 1
70 1 5166578-1 Rubber stopper (6) 1
71 1 5166578 Table end cap (pair) 1
72 1 5160837-1 Table top warning label 2

9-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

*1: Item 68 will replace item15. These two kinds of Ion-chamber have same installation procedures and
functions.

Note: If JEDI’s model number on it’s label (see the figure) is 2268970, you should follow the table
Cabinet 1. If the number is 2244165-2, you should follow the table Cabinet 2.

Item # FRU GPCP NO. Description Quan.

Level
Cabinet 1
1 1 2375230 System I/F Board (replace System I/F Board 1
2259298-45 and CAN I/F Board 2259298-46)
CAUTION
The System I/F board 2375230
can be used together with Rev2.14 of the
System Console Software (2286799-16,
Item #3 of Console).
2 1 5164678 No Fuse Breaker 690V 100A 1
3 2 2259298-113 Contactor S-N95 150A/690V AC100V 1
4 1 2259298-114 Spark Killer CR-50500 1
5 1 2259298-115 Fuse RS414-061 10A/500V 1
6 1 2259298-116 Fuse RS414-055 5A/500V 1
7 1 2259298-117 Fuse Holder FZRRAZ N091483 32A/690V 2
8 1 2259298-41 Fuse Holder 7
9 1 2259298-121 Fuse 61NM 6.3A/250V 1
10 1 2226325-9 Fuse 61NM 2.5A/250V 3
11 1 2226325-10 Fuse 61NM 5A/250V 1
12 1 2226325-11 Fuse 61NM 8A/250V 2
13 2 2259298-118 Fuse Holder SI 000 DIN 80 3
14 1 2259298-119 Fuse 6.6gRB 000 DO8V/125 3
15 1 2259298-123 Noise Filter 2
16 2 2259298-124 Terminal block SAK 2.5 EN Assy
17 1 2259298-122 Mov Board Assy 1
18 1 2226325-8 Spark Killer 150VAC 0.3μF 150Ω 1
19 2 2259298-120 Contactor S-N10 20A/690V AC100V 1

9-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
20 1 2259298-127 Relay LY2 110VAC 1
21 1 2259298-128 Relay LY1 12VDC 1
22 1 2226325-6 Relay LY2 12VDC 1
23 2 2259298-39 Relay Socket 3
24 1 2259298-34 SW power supply 12V, 5A 1
25 1 2259298-35 SW power supply +5V, ±12V, 25W 1
26 1 2259298-126 Noise Filter ZGB2202-01U 250V/2A 2
27 1 2259298-44 DC Power Board 1
28 2 2259298-32 Transformer 1.9kW Input:360/480V 1
Output:24/240V
29 2 2259298-112 Transformer 400VA Input:360V/480V 1
Output:100V
30 2 91651653 Bucky Connector 1
31 1 2281982 Tomo I/F PCB 1
32 1 2226325-9 Fuse (for MX100 X-ray tube fan and SG100 2
Wall Stand)
33 1 2372633 Power filter 1
34 2 221-2742 L side panel assy. 1
35 2 221-2744 R side panel assy. 1
36 2 221-2746 Back side panel assy. 1
37 2 221-2748 Front side panel assy. 1
39 2 2259973-1 Proteus System Cabinet (32KW) 1
40 2 2259973-2 Proteus System Cabinet (50KW) 1
41 2 2259973-3 Proteus System Cabinet (65KW) 1
42 2 2259973-4 Proteus System Cabinet (80KW) 1
43 2 2215674 Rotor Capacitor Set 1

Item # FRU GPCP NO. Description Quan.

Level
Cabinet 2
1 1 2226325-4 No fuse breaker 480V 50A 1
2 1 2226325-8 Spark killer 150VAC 0.3μF 150Ω 1
3 1 2226325-3 Contactor S-N50 600V 50A 1
4 2 2259298-41 Fuse holder 7
5 1 2226325-11 Fuse 8A/250V 1
6 1 2226325-10 Fuse 5A/250V 2
7 1 2226325-9 Fuse 2.5A250V 4
8 2 2259298-40 Fuse holder 2
9 1 2259298-33 Fuse 10A500V 1
10 1 2226325-12 Fuse 2A/500V 1
11 2 2259298-43 Fuse holder 1
12 1 2259298-42 Fuse 125A/1000V 3
15 1 2226325-7 Noise filter 2
16 1 2226325-6 Relay 220VAC 10A and 24VDC 10A 2
17 2 2259298-39 Relay socket 2
18 1 2259298-35 SW power supply +5V, ±12V, 25W 1
19 1 2259298-34 SW power supply 12V, 5A 1
20 1 2259298-44 DC power board 1

9-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
21 2 2259298-32 Transformer 1.9kW Input:360-480V Output:24- 1
240V
22 2 2226325 Transformer 250VA Input:360/480V 1
Output:100V
23 1 2281982 Tomo I/F PCB 1

Item # FRU GPCP NO. Description Quan.

Level
Wall
Stand
1 1 2259298-47 EM locks ( pair ) 1
2 1 2259298-51 Hand grip switch 2
3 (1) 1 2189553-2 Bucky(RH) 1
3 (2) 1 2189553 Bucky(LH) is same as Table Bucky (LH) 1
4 1 2259298-30 Bearing 8
5 1 2259298-92 Steel Cable 2
6 2 2259298-93 Rail Bearings ( pair ) 1
7 2 2259298-96 Fixed grid (10:1 180cm 60l/cm) 1
8 2 2259298-49 Bucky grid (10:1 180cm 43l/cm) 1
9 2 080-1008-22 Grid 1
10 2 080-1009-22 Grid 1
11 1 603-3220 Steel Cable (for the wall stand with a knee 1
spacer)
12 1 021-0291 Bearing (for the wall stand with a knee spacer) 1
13 1 021-0293 Bearing (for the wall stand with a knee spacer) 1
14 2 602-3339 Hand Rest Assy (for the wall stand with a knee 1
spacer)
15 2 096-0036 Plunger(for the wall stand with a knee spacer) 1
16 1 601-3600 Power-off Protection Lock 1
17 2 604-3010 Wall Stand Bucky Cover 1
18 2 220-2125 Wall Stand Pedestal Cover 4
19 2 600-0027 Chin Rest 1
20 1 2338145 (Localized) Cassette Tray-Size Sensing 1
21 1 5159516-1 Reciprocating Bucky L/H 1
22 1 5159516-2 Reciprocating Bucky R/H 1
23 1 5166100 Step Motor 1
24 1 5166198 Circuit Board L/H 1
25 1 5166059 Circuit Board R/H 1
26 1 5166209 Rail Kit 1

9-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
27 1 5166188 250VAC, 315mA Fuse 1
28 1 5166307 250VAC, 160mA Fuse 1
29 1 5167409 AID Ion Chamber 1
30 1 5167409-2 AID Ion Chamber with 24 meter cable 1

Note: For SG100 Wall Stand (GPCP No. 2225849) FRU, refer to SG100 Service Manual (2150297-100).
Note: For SG120 Wall Stand (GPCP No. 2402562) FRU, refer to SG120 Service Manual (Supplier Part No.
S0012532).

Item # FRU GPCP NO. Description Quan.

Level
OTS
1 2 2273436 Anode cover assy. 1
2 2 2273439-2 Cathode cover assy. 1
3 2 2273442 Top cover assy. 1
4 1 2259298-54 Auto collimator 1
5 2 2273450 Trunion scale assy. 1
6 1 2320993 OCS console 1
7 2 2273439 Cathode cover assy. 1
8 2 2278757 Top cover assy. 1
9 1 2271727 Collimator Bulb (For Auto and Manual 1
Collimator)
10 1 2271728 Fuse (1.6A 250V) 2
11 1 2271729 Tape Measure. 1
12 1 2271730 Bulb Fan 1
13 1 2307338 PCB D1 1
14 1 2307340 PCB D2 1
15(1) 1 2259981 X-ray Tube, Rad14 1
15(2) 1 2271627 X-ray Tube, Rad21 1
15(3) 1 2226680 X-ray Tube, Rad12 1
15(4) 1 D2301R (46- X-ray Tube, MX100 1
155400G281)
16 2 610-3150 Trunion used for 65, 80 kW (for Rad21) 1
17 2 2259298-95 Trunion used for 32, 50 kW 1
18 1 2259989 Manual collimator 1
19 1 241-0267 Auto collimator Terminator 1
20 1 2257211 OTS SW Power Supply 1
21(1) 2 610-3099 Mounting Plate for Collimator for Rad 12 or 14 1
21(2) 2 610-3099-02 Mounting Plate for Collimator for Rad 21 1
22 2 610-3650 Tube- Connector 2
23 2 2272214-3 Tube Cover Kit (for 65, 80kW) (for Rad21) 1
24 2 2272214-2 Tube Cover Kit (for 32,50 kW) 1

9-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
25 2 610-3173 Tube cooling fan kit for FC 2 1
26 1 610-3175 Resistor Assembly For FC2 Tube Fan 1
27 2 610-3181 Fan Set 1
28 2 2301864 R21 Tube Fan Installation Manual 1
29 1 2318537 OCS Console Button Kit 1
30 2 221-2995 APR Back-up Floppy Disk (set) 1
31 2 241-2703 AEC Fast Calibration Floppy Disk 1
32 2 2303649 Jedi 80 R1T/Rad21 with Fan SW Disk 1
33 2 008-8002 M5X12 Socket Set Screw From Bossard 4
34 1 2325424 Collimator Plastic Front Cover 1
35 1 2345789 Collimator display 1
36 1 2348513 Thermal Switch For Tube Rad 12,14&21 1
37 2 2273368 Condor/F.C. bottom tube Cover 1
38 2 2273371 Condor top tube cover ASM 1
39 2 2273365 Condor anode end bracket 2
40 2 2273366 Condor cathode end bracket 2
41 2 2365447 Cable bracket 1
42 2 2364939 Spacer of tube mount 1
43 2 2352540 Extended Tomo-link Yoke 1
44 1 2372800 Cone Assembly with lable 1
45 1 2379458 Lead cup Assy. for MX100 X-ray tube N
46 1 2375334 Condor UIF to Tube (MX100) Mounting Bracket 1
47 1 2375342 Collimator Mount Ring for Condor (for MX100 1
tube)
48 1 2375344 Ring to Retain Collimator Mount Ring (for 1
MX100 tube)
49 1 2375341 Collimator Mount Retainer Condor (for MX100 4
tube)
50 1 2375320 Spacer for Condor UIF Bracket (for MX100 1
tube)
51 N 2364938 Condor User Interface Condor BRKT (for 1
MX100 tube)
52 2 2278999 FC2 Connecting Bracket 2
53 2 46-208765P36 Tube Cover clamp 1
54 2 2269030-10 GE logo 1
55 N 2383309 Aluminium Plate 1
56 1 2271734 Manual Collimator D7 Electronic Board 1
57 1 2399471 Auto Collimator AL-07F Detent Handle 1
58 1 2278999 Tube Cover Adapter Bracket 1
59 1 2379827 Eclipse Proteus Collimator 1
60 1 2383312 Eclipse Proteus Collimator Control Board 1
61 1 2383313 Eclipse Proteus Collimator User Interface Board 1

9-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
62 1 2377082 Eclipse Proteus Collimator Lamp 1
63 1 2383804 Eclipse Proteus Collimator Bucky Centering 1
Laser
64 1 2385357 Eclipse Proteus Collimator LCD Display 1
65 1 2383805 Eclipse Proteus Collimator Tape 1
66 1 5126798 APR backup floppy disk for 65kW and 80kW 1
67 1 610-3170 Tube ground clamp 1

Note: If the site needs to install the tube fan kit, Please use S3918LZ to order item #25,
item #28 and item #32 together.

Item # FRU GPCP NO. Description Quan.

Level
Console
1 1 2259976 System console 1
2 2 2260190 Console printer kit 1
3 1 2286799-16 System Console Software Disk V2.14 1
Note: Please order new System
Console Software Disk no matter
what part number on the original
disk is, and then, replace the
original version with Rev 2.14.

CAUTION The Rev 2.14 of the System

Console Software 2286799-
16 can be used together with either the
System I/F board 2375230 (Item #1 of
Cabinet 1) or the System I/F Board
2259298-45 and CAN I/F Board 2259298-
46.
4 2 098-0031 System console exposure hand switch 1
5 1 5178302 System console warning label 1
6 1 2382506 FC Spanish label kit 1

Item # FRU GPCP NO. Description Quan.

Level
Cables
1 1 2259298-56 Table height cable SID cable 1
2 1 2259298-57 Table power cable 1
3 1 2259298-58 Cassette size sensing cable 1
4 1 2259298-60 System console cable kit 1
5 1 2259298-63 Bucky control cable 1
6 1 2259298-65 Wall stand power cable 1
7 1 2259298-73 Grounding Wire 2
8 2 221-2734 Tomo CAN & RTL Cable 1
9 2 221-2996 Tomo Interface Cable 1
10 2 221-2997 Table/Tomo Interface Cable 1

9-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Item # FRU GPCP NO. Description Quan.

Level
11 2 221-2999 Tomo-link Power Cable 1
12 2 241-0266 Manual Collimator Cable 1
13 2 221-2736 WS Lock Power Cable 1
14 2 46-173995P11 Cable 1
15 2 46-173995P12 Cable 1
16 2 421-0001-02 Fan Cable 1
17 2 421-0001-03 Fan Earth Cable 1
18 2 221-3011 Table Inter SID Cable 1
19 2 221-3020 Table Inter Power Cable 1
20 2 221-3008 Lim_BD I/F Cable 1
21 2 221-3004 Front Peda1 I/F Cable 1
22 2 221-3005 Back Peda1 I/F Cable 1
23 2 221-3016 2nd Safety SW Cable 1
24 2 221-3018 Logic_BD Power Cable 1
25 2 221-3012 Table Control Cable (1) 1
26 2 221-3017 Table Control Cable (2) 1
27 2 221-3013 Table Locks Cable (1) 1
28 2 221-3014 Table Locks Cable (2) 1
29 2 221-3015 Dis_SW Cable 1
30 2 221-3025 Emerg. SW Cable 1
31 1 600-3033 Wall Stand Power OFF Lock Power Cable 1
32 N 2365706 MX100 tube fan power cable 1
33 1 2259298-66 Table grounding cable 1
34 1 2267582 Cable Conceal Assembly (Long) 1
35 1 2267582-2 Cable Conceal Assembly (Short) 1
36 1 221-2892 Cabinet grounding cable (4) 1
37 1 5166224 Cassette Size Sensing cable 1
38 1 5166260 Power cable 1
39 1 5166654 24m Interconnecting cable for AID Ion 1
Chamber

9-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-1
Table Illustrated Parts (1)

Item# 1

Item# 7

Item# 9
Item#48,49

Item# 8 Item# 2 Item# 4

Item# 6 Item# 5

Item# 53 (the
spring leaf under
the button)

Item# 11

Item# 52

Item# 51

Item# 12

Item# 13

9-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-2
Table Illustrated Parts (2)

Item# 15
Item# 14

Item# 17 Item# 18 & 19 Item# 20

Item# 16

Item# 22

Item# 21

Item# 23

9-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-3
Table Illustrated Parts (3)

Item# 24 Item# 25 Item# 26

Item# 27
Item# 28

9-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-4
Table Illustrated Parts (4)

Item# 29
Item# 33
Item# 3

Item# 32 Item# 30
Item# 48
Item# 47

Item# 31

Item# 34

Item# 35

Item# 38

Item# 36

Item# 71

Item#37

Item# 70
9-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-5
Table Illustrated Parts (5)

Item# 40
Item# 39

Item# 42

Item# 41

Item# 44

Item# 43

Item# 72 Item # 58

9-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-6
Table Illustrated Parts (6)

Item# 45

Item# 46

Item # 56

Item # 68
Item # 55

Item # 59

Item # 69

Item # 57

9-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Item # 65
Illustration 1-7
Table Illustrated Parts (7)

Item # 62

Item # 60 Item # 61

Item # 66/67

Item # 63

Item # 66/67

Item # 64

9-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-8
Cabinet 1 Illustrated Parts (1)

Item# 1

Item# 6 Item# 5

Item#4

Item#7
Item# 2
Item# 3
Item# 13

Item# 8

Item# 14
Item #32
Item# 10 Item# 12

Item# 9 Item# 11

9-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-9
Cabinet 1 Illustrated Parts (2)
Item# 16

Item# 15 Item# 30

Item# 17
Item# 18

Item# 19

Item# 20
Item# 24

Item# 23

Item# 25

Item# 26

Item# 21 Item# 22
Item# 27

Item#31

Item#28
Item#29
Item# 33

9-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-10
Cabinet 2 Illustrated Parts (1)

Item# 2

Item# 1

Item# 3

Item# 5 Item# 6 Item# 7 Item# 9 Item# 10

Item# 11

Item# 12

Item# 4 Item# 8

9-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-11
Cabinet 2 Illustrated Parts (2)

Item# 15

Item# 18
Item# 19
Item# 16

Item# 20
Item# 17 Item# 22

Item# 23

Item# 21
9-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-12
Wall Stand Illustrated Parts (1)

Item # 3
Item# 1 Item # 2

Item # 12 Item # 13

Item# 4 Item# 5, 11 Item # 6

Item # 7, 8, 9, 10 Item # 15
Item # 14
Item # 19

Item# 19
Item # 16 Item # 20

Item # 18 Item # 17

9-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-13 Item # 26

Wall Stand Illustrated Parts (2) Item # 29

Item # 23

Item # 30

Item # 21 Item # 22

Item # 27/28

Item # 24

Item # 27/28

Item # 25

9-22
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-14
OTS Illustrated Parts (1)

Item# 1

Item# 2

Item# 3

Item# 5

Item# 54

Item#7

Item# 4 Item# 6

Item# 53

Item# 8

Item# 52

Item# 9

9-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-15
OTS Illustrated Parts (2)

13
10
14
10

11

Item#19

Item# 60
Item# 61
12

Item# 63

Item# 59

Item# 15 Item# 16 & 17

Item# 64 Item# 65

9-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-16
OTS Illustrated Parts (3)

Item 20
Item 33
Item# 21

Item# 22
Item# 24

Item# 23

Item# 34
Item# 29 Item# 55
Item# 35

9-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-17
OTS Illustrated Parts (4)

Item #27

Item #25
Item #67
Item #26

Item #38

Item #39

Item #40

Item #37

9-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-18
OTS Illustrated Parts (5)

Item #41 Item #42

Item #43
Item #44

Item #45
Item #48

Item #47
Item #51
Item #49
Item #46

Item #50

9-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration 1-19
OTS Illustrated Parts (6)

Item #58

Item #57

Illustration 1-20
Console Illustrated Parts

Item #6

Item #1
Item #2

Item #4

9-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 2
JEDI GENERATOR RENEWAL PARTS

2-1 Introduction
This section provides information for the identification of Renewal Parts for the
Jedi 50Plus R1T generator
BEFORE ORDERING A SPARE PART, BE SURE TO KNOW THE JEDI
WARNING
GENERATOR YOU HAVE ON SITE.
The model number of the Jedi generator is localized on rating plate on Auxiliary
module (see page 10-24 Jedi Generator Illustration: labelling)
If the model number is 2244165 you have a JEDI 50plus R 1T.
If the model number is 2268970 you have a JEDI 80 R 1T
Order the spare part according to the JEDI generator you have.
If only one part number is written order this one, otherwise order the spare part
according to your generator
When replacing the Jedi Generator, pay attention to check the GPCP No. of the Rotation
CAUTION
Capacitor Set of the Auxiliary Module of Jedi Generator (refer to Job Card D/R JEDI 1, D/R
JEDI 17-38) and ensure its correct match with the X-ray tube type. Pay attention to
download and upgrade the Jedi software (Refer to Job Card SW JEDI 7-2 in Chapter 4.).

For Rad 14,21 X-ray tube, the GPCP No. should be 2250002.

For MX100 X-ray tube, the GPCP No. should be 2215674.

Replace the Rotation Capacitor Set when necessary.

2-2 FRU Information

Information shown for each FRU (Field Replaceable Unit) is explained below.

9-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Wherever possible, the FRU or its position is illustrated for easy indentification.

2-3 Renewal Parts

The System I/F board 2375230 can be used together with Rev2.14 of the System Console
CAUTION Software (2286799-16, Item #3 of Console).

The Rev 2.14 of the System Console Software 2286799-16 can be used together with
either the System I/F board 2375230 (Item #1 of Cabinet 1) or the System I/F Board
2259298-45 and CAN I/F Board 2259298-46.

9-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration – JEDI 50Plus R 1T and JEDI 80R 1T Generator Location of Main Assemble FRU2: 2244165.
Miscellaneous Items:
First aid spares: (FRU: 1) GPCP No. 2217057 Services tools (FRU: 2)
1 PLASTIC ZIP LOCK BAG 160X220 10 TY-WRAPS D22/L99X2.5 Service software
10 SCREW HEX FLANGE HEAD M4X8 1 SHORT CIRCUIT CABLE 9-wire serial cable, No. 2207478
SCREW HEX FLANGE HEAD 4MM 8MM 1 CONNECTORS KIT FOR FC2 For JEDI 50Plus R 1T: 2244165-2
SCREW HEX FLANGE HEAD 5 MM 12 2 PLASTIC ZIP LOCK BAGS For JEDI 80R 1T: 2268970
MM 40X60
1 FUS FF 14X51 15A 700VDC C 50KA 3 PLASTIC ZIP LOCK BAGS
ULR 80X120
1 FUS FF 14X51 2A 700VDC C 50KA 1 RECT CONNEC 9C FEM
ULR AWG14 SCREW
1 SLOW BLOW FUSE HCP 6X32 10A 10 SCREW HEX FLANGE
250V UL HEAD 5 MM 12 MM
1 PADDED BAG W/ ADH CLOSURE
260X370

9-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration – JEDI 50Plus R 1T and JEDI 80R 1T AC/DC Unit, Interface Unit & Auxiliary Unit

Jedi 50plus R 1 T:2214995

Jedi 80R 1T: 2269396
FRU: 1
Jedi 50plus R 1 T:2209840 Job Card D/R JEDI 17-40
Jedi 80R 1T: 2209840-2
FRU: 1
Job Card D/R JEDI 17-39

Bucky Connector
91651653 FRU: 2
AEC Board V2
2226456-3 2222253-3
FRU: 1 FRU: 1
Job Card D/R JEDI 17-47 Job Card D/R JEDI 17-46

Rotor Capacitor
2250002 (2215674 for MX
100 X-ray tube)
FRU: 2
Job Card D/R JEDI 17-38

9-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2265276

-2

Illustration – JEDI 50Plus R 1T and JEDI 80R 1T Power Unit

9-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

2-4 Cables

1 CAN cable 5 Inter Modules cable

2249990 2249998 for JEDI 50Plus R 1T 2244165
2249998-2 for JEDI 80R 1T 2268970
FRU: 2 FRU: 2
2 Heater/AUX. Module AC-DC/Inverter DC bus cable
2215839 2249988
FRU: 2 FRU: 2
3 K VPS-Heater strap Supply Y/EMC Board cable
2215227 2221733
FRU: 2 FRU: 2
4 ROT/LVPS/Heater cable L VPS-Rotation strap
2215903 2215228
FRU: 2 FRU: 2

9-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1 CAN cable 5 KV Measure – Gate Comd 9 AC/DC – bus cable

cable
2249990 2198185 2249988
FRU: 2 FRU: 2 FRU: 2
2 KV Control – I/F RAD cable 6 Quad Snub / Gate Comd cable Inverter module cable
2202418 2249993 2249998 for JEDI 50Plus R 1T
2244165
2249998-2 for JEDI 80R 1T 2268970
FRU: 2 FRU: 2 FRU: 2
3 AEC cable Assy 7 KV Meas. – Inv Filament cable I/F – AEC cable (option)
2208000 2249992 2202419
FRU: 2 FRU: 2 FRU: 2
4 KV Meas. – KV Control cable 8 Inverter DC bus cable TAV cables
2250036 2249994 2207478
FRU: 2 FRU: 2 FRU: 2

9-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

This page intentionally left blank.

9-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SECTION 3
JEDI GENERATOR DISASSEMBLY/REASSEMBLY

3-1 Introduction

This section provides information to dismount and remount FRU (Field

Replaceable Unit).

3-2 TOOLS

Serviceability of Jedi Generator requires the following tools:

K
Digital multimeter (A)
Philips screwdriver (B)
Allen key (C) J
Screwdriver with interchangeable socket head (D)
Long extension for ratchet wrench (E) I
F
Short extension for ratchet wrench (F)
Cutting pliers (G)
High Voltage wrench (H)
Ratchet wrench (I) C
Socket wrench (J) E
A
Hexagonal head socket set (K).

D G
B H

9-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/5 D/R JEDI 1

subassembly: JEDI Modules Disassembly/Reassembly

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:
from / / from Time:
to / / to

1 INTRODUCTION
Jedi Generator are consist of four modules. Each module can be disassembled from the system.

AC/DC Auxiliary
Unit Unit

Power Interface
Unit Unit

9-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/5 D/R JEDI 1

2 REMOVE THE AUXILIARY MODULE

1. Disconnect all cables on the system interface

board, then demount system interface board.

2. Disconnect the connectors and ground cables

on top of the Auxiliary module.

3. Disconnect the flat ribbon cable from Jedi kV

Control Board.
Flat Cable

Left Side Right Side

4. Remove the three fastening screws on both side

of the Interface Module.

5. Take out the Auxiliary module from the front side.

6. Reassemble the Auxiliary Module.

9-39
Screws
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/5 D/R JEDI 1

3 REMOVE THE AC/DC MODULE

1. Remove the Auxiliary Module firstly.

2. Disconnect the connectors on top of the AC/DC

module.

3. Disconnect the power cables and ground cables.

4. Disconnect the DC-Bus cable on Inverter

Module.
Power and
Ground

5. Remove the 4 fastening screws on both side of

the AC/DC module.

6. Pull out the AC/DC. DC-Bus

7. Reassemble the Auxiliary and AC/DC Modules.

Screws

9-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/5 D/R JEDI 1

3 REMOVE THE INTERFACE MODULE

1. Disconnect the connectors on left side. (AEC,
Bucky, Generator communication and Door light)

2. Remove the five screws from the left side of the

Interface module.

Screw

3. Disconnect the Power Cable and Communication

Cable from Jedi Interface Board.
Power Cable
Disconnect Jedi kV Control Board flat cable.

Communication KV Control
Cable Cable

4. Remove the four screws from the top of the Interface

module.

5. Remove the five screws from the right side of the

Interface module.

6. Pull the Interface module forwards to take out the

Interface module. Pull Forwards
Screws
7. Reassemble the Interface Module.

9-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/5 D/R JEDI 1

4 REMOVE THE INVERTER MODULE

1. Disconnect all cables on the Interface module.
(AEC, Bucky, Generator communication and
Door light)

2. Disconnect DC power cable and ground cable

on left side of the Inverter module.

3. Unplug the HV Cables from the socket.

4. Remove the two screws from the bracket.

5. Remove the two screws from the bracket.

6. Remove the two screws from the front side of

main bracket.
7. Push Interface and Inverter modules forwards
and take out the unit.
8. Demount the screws fastening Interface module
with the Inverter module. (see 4/5)
9. Reassemble the Interface module and Inverter
module.

9-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/8 D/R JEDI 17-37

subassembly: HV Tank or Inverter Power Supply

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 2h 00min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 mm Allen wrench.
13 mm socket with ratchet.
C–clamp for HV connections.
Multimeter.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

Check with the Multimeter in DC mode that the voltage is below 10 V between “+” and “-”
CAUTION terminals on the Power Unit (see below). IF NOT, WAIT UNTIL VOLTAGE BECOME O V
BEFORE REMOVING CABLES.

To protect the circuit boards, do not forget to wear the antistatic bracelet.

9-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/8 D/R JEDI 17-37

4 PREREQUISITES

THE WHOLE INVERTER UNIT WEIGHTS 30 KILOGRAMS (66 POUNDS). TWO PEOPLE
WARNING
ARE REQUIRED TO CARRY IT.

5 DISASSEMBLY

5-1 Remove the Inverter Unit

THE POWER UNIT WEIGHTS 30

WARNING KILOGRAMS (66 POUNDS). DO NOT
TRY TO LIFT IT WITHOUT
ASSISTANCE

1. Disconnect the HV cables, console, AEC and buckies

cables.

2. Disconnect the flat wide ribbon cable 1 from J1 on the Inverter

Unit
Auxiliary Unit.

3. Disconnect “+” and “-” cables 2 .

4. Disconnect the cable from J3A 3 and the cable from

J3 QUAD SNUB 4 .

5. Unscrew the 5.5 mm screw holding the Ground cable

5 .

6. Remove the Inverter Unit from the cabinet.

5 4

1
3
9-44
INVERTER UNIT
TOP VIEW
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/8 D/R JEDI 17-37

5-2 Remove the Interface Unit box

1. Unscrew twelve 5.5 mm screws that retain the cover

panel and remove this one 1 .
1

2. Disconnect the flat wide ribbon cable 3 from J1 of the 2

KV Control Board 4 .

3. Unscrew twelve 5.5 mm screws 2 securing the

Interface Unit box to the Power box.

4. Remove the Interface Unit box.

3 J1 4

5-3 Remove the HV tank or the Inverter Power Supply

1. Unscrew the 5.5 mm screws securing the two EMC

cover panels 1 at the HV connections side and
remove them.

Take great care not to let screws fall into 1

NOTICE
the HV connector receptacles. Cover
them with plastic caps.

9-45
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/8 D/R JEDI 17-37

2. Disconnect the cable 2 connected to J3 on the KV

Measure Board.

3. Disconnect the ribbon cable 3 connecting J2 on the

KV Control Board (Inverter Assembly) to J2 on the KV
Measure Board (HV Tank).

4. Disconnect the ribbon cable 4 connecting J3 on the 5 3

Gate Command Board to J1 on the KV Measure Board
(HV Tank).

5. Using a 13 mm socket wrench, remove the four nuts

5 holding the Primary coil flat cables.
4

6. Disengage the end of Primaries coil flat cables from

their screw and re-enter them towards the interior.

7. Remove the 5.5 mm screws: three at the front side 6

(two at right, one at left) and three at the right side 7 .

8. At the rear side, remove the eight 3 mm Allen screws

8 which secure the heat sink of the Inverter Power 6
Assembly to the HV Tank.

9. Remove carefully upwards the Power Unit. 8

7

9-46
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/8 D/R JEDI 17-37

10. Take off the assembly constituted by: EMC covers, Coils Inverter Assy, Capa Inverter Assy, and KV Control
Board. The HV Tank 9 and the Inverter Power Assembly 10 are now free .

10

In case of change the Inverter Power Assembly, you must recover the KV control Board
NOTICE 11 and mount it in the new Inverter Power Assembly.

- Disconnect the Flat ribbon cable 12 J2.

- Remove the seven 5.5 mm screws 13 and recover the KV Control Board.

12
13

11

9-47
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 6/8 D/R JEDI 17-37

6 REASSEMBLY

Reverse the disassembly procedure to reassemble and replace the unit.

1. Reassemble the HV Tank with the other elements of the Power Unit (refer to section 5–3 9 , 10 ).

2. Mount the flat cable J1 on the KV Measure Board of the HV Tank (refer to section 5–3 4 ).

3. Mount the eight 3 mm Allen screws to secure the heat sink of the Inverter Power Assembly to the HV Tank.
(refer to section 5–3 8 ).
Tighten to torque 8 N.m (80 kg.cm).

4. Put back the 3 front 5.5 mm hex head screws (refer to section 5–3 6 ), one at the left side, two at the right
side.
Tighten to torque between 1.5 to 2 N.m (15 to 20 kg.cm).

5. Reconnect the ribbon cable from J1 on the KV Measure Board to J3 on the Gate Command Board (refer to
section 5–3 4 ).

6. Using the 13 mm socket wrench, connect the primary coil flat cables to the four capacitors 1 .

Respect the position of the two flat cables with white bands on them (refer to illustration
CAUTION above).
Make sure the presence of the IGBT Middle point 2 .

White
BAND

White
BAND

9-48
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 7/8 D/R JEDI 17-37

7. Reconnect the cable to J3 on the KV Measure Board (refer to section 5–3 2 ).

Tighten the nuts to torque 8 N.m (80 kg.cm).

8. Reconnect the wider short ribbon cable from J2 on the KV Control Board to J2 on the kV Measure Board
(refer to section 5–3 3 ).

9. Mount the 5.5 hex head screws securing the two EMC covers to the HV Tank on the HV outlet side (refer to
section 5–3 1 ) and the three screws on the other side (refer to section 5–3 7 ).
Tighten the screws to torque between 1.5 to 2 N.m (15 to 20 kg.cm).

10. If Inverter Power Assembly has been changed, reverse the disassembly procedure to reinstall the KV Control
Board (refer to section 5–3 11 ).
Tighten 5.5 mm screws to torque between 1.5 to 2 N.m (15 to 20 kg.cm).

THE POWER UNIT WEIGHTS 30 KG (66 POUNDS).

WARNING

11. Remount the Interface Unit following the inverse procedure indicated in section 5–2.
12. Remount the Module in the Cabinet following the inverse procedure indicated in section 5–1.

Be sure to place the Flat ribbon cable 3 J3 KV Control Board at the right position, see
NOTICE
illustration below.

9-49
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 8/8 D/R JEDI 17-37

CAUTION Be sure to place the “+” and “-” DC BUS in the right connector.

13. Put 5 cl of oil into the HV receptacles. Reconnect Console, buckies and AEC cables.

7 VERIFY
Connect the service laptop (refer to page 4-26 ”Service Software User Guide” JOB CARD) and proceed to ”HV no
load diagnostics” to ensure correct operation.
Skip steps ”Gate Command and Inverter in Short Circuit” diagnostics.

9-50
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 D/R JEDI 17-38

subassembly: Rotation Capacitors Set 23/56 (Rotation Capacitor Set 23/23 for MX100 X-ray tube)
purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

Note: When installing the system, do not use the capacitors in accessories crate #4 (refer to form “Crate
dimensions & weight” on page 2-5 in Chapter 2) for installation. Pay attention to pick out and
dispose the capacitors in accessories crate #4. Ensure the eco-friendly disposal of the capacitors.

1 SUPPLIES

None.

2 TOOLS

5.5 mm hex nut driver or socket wrench with ratchet.

Cutting pliers.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

The Rotation Capacitors are in the Jedi Generator Auxiliary Unit (10 kg).
On the Auxiliary Unit, disconnect internal CAN cable, DC BUS, heater cable, and Tube cable.

9-51
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 D/R JEDI 17-38

5 PROCEDURE

5-1 Remove the Auxiliary Unit Cover

The removing of the Rotation

NOTICE
Capacitors can be done without
removing the Auxiliary Unit from the
Auxiliary
Cabinet. Unit

Unscrew the sixteen 5.5 mm hex head screws and remove

the cover on the Auxiliary Unit.

5-2 Remove the Rotation Capacitors

Rotation
Capacitors 2
1. Cut the tie-wraps 1 1

1
2. Disconnect both capacitors 2 2

3. Remove the two Rotor Capacitors.

9-52
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 D/R JEDI 17-38

6 REASSEMBLY

Reverse the disassembly procedures to reinstall the Rotor Capacitors.

Use the tie–wraps from the Accessory Spares Set to reattach the capacitors.

1 2

Ensure that the capacitors are correctly connected :

For Rad14,21 tube:
1
- connect the left capacitor 20 µF to the board with cable 2259373
connect the two cable terminals marked “C20 UF” to the below pins of the left capacitor 20 µF
connect the two cable terminals marked “CF 9” and “CF 10” to CF9 and CF10 on the board, respectively.

2
- connect the right capacitor 6.4 µF to the board with cable 2259372
connect the two cable terminals marked “C6.4 UF” to the upper pins of the right capacitor 6.4 µF
connect the two cable terminals marked “CF 11” and “CF 12” to CF11 and CF12 on the board,
respectively.
For MX 100 tube:
1
- connect the left capacitor 12.6 µF to the board with cable 2215658
connect the two cable terminals marked “C12.6 UF” to the below pins of the left capacitor 12.6 µF
connect the two cable terminals marked “CF 9” and “CF 10” to CF9 and CF10 on the board, respectively.

2
- connect the right capacitor 10.5 µF to the board with cable 2215659
connect the two cable terminals marked “C10.5 UF” to the upper pins of the right capacitor 10.5 µF
connect the two cable terminals marked “CF 11” and “CF 12” to CF11 and CF12 on the board, respectively.

9-53
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 D/R JEDI 17-38

CAUTION Pay attention to check the GPCP No. of the Rotation Capacitor Set and ensure its correct
match with the different X-ray tube type.

For Rad 14,21 X-ray tube, the GPCP No. should be 2250002.

For MX100 X-ray tube, the GPCP No. should be 2215674.

Replace the Rotation Capacitor Set when necessary.

7 VERIFY

Verify that the system functions correctly.

Remount the cover. Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).

9-54
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 D/R JEDI 17-47

subassembly: I/F Board RAD

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

THE WHOLE INVERTER UNIT WEIGHTS 30 KILOGRAMS (66 POUNDS). TWO PEOPLE
WARNING
ARE REQUIRED TO CARRY IT.

9-55
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 D/R JEDI 17-47

5 DISASSEMBLY

The I/F Board Rad is situated in the Interface Unit.

The removing of the I/F Board Rad can

NOTICE
be done without removing the
Interface Unit from the Cabinet.

Interface
Unit

1. Unscrew twelve 5.5 mm screws that retain the cover

panel and remove this one 1 .

2. Disconnect the flat ribbon cable 2 and the two cables

3 , if existing, coming from the AEC Board (option).
3

3. Disconnect the flat wide ribbon cable J10 coming from

the KV Control Board 4 .
4

9-56
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 D/R JEDI 17-47

4. Remove the four screws of connectors J8 and J9 5 .

5. Remove the ten 5.5 mm screws 6 securing the

Interface Board Rad; remove the board. 5

6 REASSEMBLY

1. Reverse the disassembly procedure to reassemble the unit. Tighten screws to torque between 1.5 and 2 N.m
(15 to 20 kg.cm).

2. Power the system on and verify that the system functions properly.

9-57
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/5 D/R JEDI 17-48

subassembly: KV Control Board

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 45min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

10 mm Allen wrench.
13 mm socket with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

THE WHOLE INVERTER UNIT WEIGHTS 30 KILOGRAMS (66 POUNDS). TWO PEOPLE
WARNING
ARE REQUIRED TO CARRY IT.

The KV Control board contains a saved memory Database with essentially the following parameters:
- Tube configuration parameters, AEC calibration parameters, and Room configuration (workstation, AEC,
screen film pairs).
- Filament aging variable
- Error Log
- Recorded parameter data
If it is possible, backup database first. Else, the diagram hereafter helps you to determine the action to take for
your situation.

9-58
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/5 D/R JEDI 17-48

First

Configura* Calibration Save Non KV Control

tion Volatile RAM Out of Order
Database

DB Is
Upload Yes Upload No original DB No
Database Possible? saved?
(*)
Yes

Replace Replace Replace

KV Control KV Control KV Control

SW No Download Yes SW Yes SW

OK? Software OK? OK?

Yes No No

Download Download
Software Software

Download Configura-
Download Original
Database tion if appli-
Database cable
(*)

Calibrate if
applicable

Reset
Database:
* Date
* Time
*Clear Error
log

Operational
Checks

Save Non
Volatile RAM
Database

(*) or most recent END

9-59
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/5 D/R JEDI 17-48

5 DISASSEMBLY

The KV Control Board spare is pre-loaded with NP/NP+ software.

NOTICE
It will be required to download the software that is on site.
DATABASE RESTORE IS MANDATORY.

The installation of the KV Control

NOTICE
Board can be done without removing
the Inverter Unit from the Cabinet.

Interface
Unit

9-60
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/5 D/R JEDI 17-48

5-1 Remove the Interface Unit box

1. Unscrew twelve 5.5 mm screws that retain the cover

panel and remove this one 1 .
1

2. Disconnect the flat wide ribbon cable 3 from J1 of the 2

KV Control Board 4 .

3. Unscrew twelve 5.5 mm screws 2 securing the

Interface Unit box to the Power box.

4. Remove the Interface Unit box.

3 J1 4

5-2 Remove the kV Control Board

1. Disconnect the cables from J2 and J3 on the kV

Control Board 1 .

1
2. Remove the seven 5.5 mm hex head screws 2 which
secure the kV Control Board; remove the board .
2

9-61
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 5/5 D/R JEDI 17-48

6 REASSEMBLY

Reverse the disassembly procedure to reinstall the KV Control board and the Interface Unit.
Tighten 5.5 mm screws to torque between 1.5 and 2 N.m (15 to 20 kg.cm).

7 VERIFY

1. Connect the Service Laptop (refer to page 4-32 ”Service Software User Guide” JOB CARD)

2. Reapply power and verify that the 8 LEDs on KV Control board are scrolling.

3. Verify software version (service floppy, menu 5)

- If it corresponds to the software version on the floppy delivered with the equipment (or upgraded by FMI),
proceed to Database Restore (refer to page 4-86 ”Backup & Restore Database Setup Parameters”
Calibration Job Card).
- If not, download the software and proceed to ”Software Download / Upgrade” Job Card.

4. Restore Database (refer to page 4-86”Backup & Restore Database Setup Parameters” Calibration Job Card)
- Up-to-date database if available
- Most recent or originally saved Data Base if available
- Default one from the floppy delivered with the equipment in the Service Tool set.

Alternately, you may try to swap the NVRAM chip (U32) from the former to the new KV Control board to keep all
the parameters. Refer to page 8-18”Replace Non Volatile Parameters RAM” Job Card. If this chip is not involved
in the failure or the cause for replacement, it will allow to keep up-to-date data.

5. Calibrate:
- Perform several exposures on both focus in several workstation, with exposure time longer than 12.5 ms
If default database was restored, it is necessary to resume room set up (refer to page 4-52”Workstation
parameter” Calibration Job Card) and AEC calibration (if present) (refer to page 4-60” Automated AEC
Calibration” Job Card”). Then perform the checksum (refer to page 4-83”Checksum Validation” Job Card).

6. Save Database on the service floppy delivered with the equipment (refer to page 4-80”Backup & Restore
Database Setup Parameters” Job Card).

9-62
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 D/R JEDI 17-39

subassembly: EMC Board 3 Phases

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 45min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

None.

9-63
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 D/R JEDI 17-39

5 DISASSEMBLY

5-1 Remove AC/DC and Auxiliary Units Assy

1. Disconnect the flat wide ribbon cable 1 from J1 on the

Auxiliary Unit.
AC/DC and
Auxiliary Unit
2. Disconnect the cable 2 from J2 AUX.

3. Disconnect the cable 3 from J2 AC/DC.

4. Disconnect “+” and “-” cables from the Inverter Unit 5 .

5
5. Unscrew the 5.5 mm screw holding the Ground cable
4 .

6. Remove the AC/DC and Auxiliary Units assembly from

the Cabinet.

3
4

1 2

AC/DC and Auxiliary Units

ASSY
TOP VIEW

9-64
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 D/R JEDI 17-39

5-2 Remove the AC/DC Unit

1. On the top of the AC/DC Unit, disconnect the cable 2

4
from J3R 1 and J1 AC/DC 2 .

2. Remove two 5.5 mm hex head screws at the right side

and two at the left side 3 . The AC/DC Unit 4 and
the Auxiliary Unit 5 are now free.
3 3

5 1

AC/DC and Auxiliary Units

ASSY
TOP VIEW

5-3 Remove the EMC Board on AC/DC Unit

1. Remove twelve 5.5 mm hex head screws which retain

the cover. Remove that one.
1
2. Remove the three nuts 1 securing the phase cables
and three screws 2 retaining the EMC board to the
rectifier block.

3. Unscrew nine 5.5 mm hex head screws 3 , Standoff

4 and remove the EMC Board 5 .
3

5 4
2

9-65
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 D/R JEDI 17-39

6 REASSEMBLY

Reverse the disassembly procedure to reinstall the EMC board.

Tighten 5.5 mm screws to torque between 1.5 and 2 N.m (15 to 20 kg.cm).

Ensure that U1 Standoff is tighten to the torque between 1.5 and 2 N.m (15 to 20 kg.cm).
CAUTION
Refer to section 5–3 4 .
Remount the AC/DC and Auxiliary Units Assembly inside the Cabinet.

CAUTION Be sure to place the “+” and “-” DC BUS in the right connector.

7 VERIFY

Reapply power and verify the presence of 3 phases.

Verify that the system functions correctly.

9-66
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/4 D/R JEDI 17-40

subassembly: AC/DC 3 PH Power Assembly

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 45min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm socket, with ratchet if possible (to remove cover and board)
10 mm socket with ratchet (to remove DC and rectifier cables)
Large Philips screw driver (to remove cables from the rectifier block).

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
1. Insure that the neon (orange) indicator light on the board has gone out.
2. Be careful touching components on this board; some become very hot.
3. To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

None.

9-67
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/4 D/R JEDI 17-40

5 DISASSEMBLY

Note: The AC/DC 3 Phases Power Assembly is made up of two main elements: AC/DC BOARD 3
Phases and RECTIFIER BLOCK 3 Phases.

5-1 Remove AC/DC and Auxiliary Units Assy

1. Disconnect the flat wide ribbon cable 1 from J1 on the

Auxiliary Unit.
2. Disconnect the cable 2 from J2 AUX. AC/DC and
Auxiliary
Units
3. Disconnect the cable 3 from J2 AC/DC.

4. Disconnect “+” and “-” cables from the Inverter Unit 5 .

5. Unscrew the 5.5 mm screw holding the Ground cable

4 . 5

6. Remove the AC/DC and Auxiliary Units assembly from

the Cabinet.

3
4

1 2

AC/DC and Auxiliary Units

ASSY
TOP VIEW

9-68
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/4 D/R JEDI 17-40

5-2 Remove the AC/DC Unit

1. On the top of the AC/DC Unit, disconnect the cable 1

4
from J3R 1 and J1 AC/DC 2 .

2. Remove two 5.5 mm hex head screws at the right side

and two at the left side 3 . The AC/DC Unit 4 and the
Auxiliary Unit 5 are now free.
3
3

5 2

AC/DC and Auxiliary Units

ASSY
5-3 Remove the AC/DC Board on AC/DC Unit TOP VIEW

1. Remove twelve 5.5 mm hex head screws which retain - + 1

the cover. Remove that one.
2. Remove the two DC cables fastened with 10 mm nuts
1
on the board .
3. Remove two screws retaining the AC/DC board
2
to the rectifier block .
4. Remove seven 5.5 mm hex head screws 3 and lift out
the AC/DC Board 4 .
2

9-69
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 4/4 D/R JEDI 17-40

5-4 Remove the Rectifier Block

1. The Rectifier Block 1 appears after removing the EMC

Board (refer to ”EMC Board 3 Phases”
Disassembly/Reassembly Job Card sections 5–3-2 to
5–3-3) and the AC/DC Board 2 1
1. With the Allen key 3 mm, unscrew the 2 screws 2
holding the rectifier to the chassis and remove the
block.

6 REASSEMBLY

1. Reverse the disassembly procedure to reinstall the AC/DC 3 PH Mid Power Assembly and the EMC Board.
2. Tighten the 10 mm cable retaining nuts to 3 N.m (30 kg.cm), and the 5.5 mm hex head screws to 1.5 to 2 N.m
(15 to 20 kg.cm).

CAUTION Ensure cables terminals are repositioned as noticed before.

Verify that the + and - DC Bus cables are not reversed to prevent damage to the Inverter
CAUTION 1
(Refer to section 5–3 ).
The Rectifier Block has to be placed with the two poles in regard of the AC/DC Board
CAUTION 1
(Refer to section 5–4 ).

Be careful to preserve the special grease that is spread between the Rectifier Block and
CAUTION the chassis. This grease, called: Conductive Surface Compound, provides both thermal
and electrical conductivity that is important in reducing failure of the rectifier.

Be sure to place the “+” and “-” DC BUS in

CAUTION
the right connector.

3. Remount the AC/DC and Auxiliary Units Assy inside the Cabinet.

7 VERIFY
Reapply power and verify that the system functions correctly.

9-70
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 D/R JEDI 17-43

subassembly: :LV Power Supply 3 Phase Board

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm hex nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

1. Insure that the Neon N1 (orange) indicator light on the LVPS Board has gone out.

2. Be careful touching components on the LVPS Board. Some become very hot.

To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

None.

9-71
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 D/R JEDI 17-43

5 DISASSEMBLY

The removing of the LV Power Supply

NOTICE
3-Phase Board can be done without
removing the Auxiliary Unit from the
Cabinet.
Auxiliary
Unit
Unscrew the sixteen 5.5 mm hex head screws and remove
the cover on the Auxiliary Unit.

5-1 Remove the LV Power Supply Board

1 2 3
1. Disconnect the 3 cables , ,
1 from the LV Power Supply 3 Phases
4
board .

4
2. Unscrew the six 5.5 mm hex head
screws and remove the LV Power
4
Supply 3 Phase Board .

3 2 9-72
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 D/R JEDI 17-43

6 REASSEMBLY

Reverse the disassembly procedures to reinstall the LV Power Supply 3 Phases Board.

Verify that the following cables are not reversed before power ON (refer to section 5–1):
CAUTION
2
1. Cables CF2 (+DC BUS) and CF1 (- DC BUS) .
3
2. Cables CF4 (160 V) and CF3 (0 V) .

Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).
Remount the cover. Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).

7 VERIFY

Verify that the system functions correctly.

9-73
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 D/R JEDI 17-44

subassembly: :Filament Board 1 INV

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm hex nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

1. Insure that the Neon DS3 (green) indicator light on the Filament Board has gone out.

2. Be careful touching components on the Filament Board . Some become very hot.

To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

None.

9-74
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 D/R JEDI 17-44

5 DISASSEMBLY

5-1 Remove LV Power Supply Cover

The removing of the Rotation

NOTICE
Capacitors can be done without
removing the Auxiliary Unit from the Auxiliary
Cabinet. Unit

Unscrew the sixteen 5.5 mm hex head screws and remove

the cover on the Auxiliary Unit.

5-2 Remove the Filament Board

1
1. Disconnect the ribbon cable
4
1 between the Filament Board and
5 2
the LVPS Board . Disconnect
3
and the connector J2 .
5

4 2. Unscrew the six 5.5 mm hex head

screws and remove the Filament
4
Board 1 INV .

2 3
9-75
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 D/R JEDI 17-44

6 REASSEMBLY

Reverse the disassembly procedures to reinstall the Filament Board 1 INV.

2
Verify that cables CF4 (160 V) and CF3 (0 V) are not reversed before power ON (refer
CAUTION to section 5–2).

Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).
Remount the cover. Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).

7 VERIFY

Verify that the system functions correctly.

Run Heater Function Diagnostics.

9-76
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 D/R JEDI 17-45

subassembly: :Rotor Board High Speed

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 15min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm hex nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.

1. Insure that the Neon DS7 (orange) indicator light on the Rotor Board has gone out.

2. Be careful touching components on the Rotor Board. Some become very hot.

To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

None.

9-77
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 D/R JEDI 17-45

5 DISASSEMBLY

5-1 Remove Auxiliary Unit Cover

The removing of the Rotation

NOTICE
Capacitors can be done without
removing the Auxiliary Unit from the Auxiliary
Unit
Cabinet.

Unscrew the sixteen 5.5 mm hex head screws and remove

the cover on the Auxiliary Unit.

9-78
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 D/R JEDI 17-45

5-2 Remove the Rotor Board

1. The Auxiliary Unit being free, unscrew ten 5.5 hex head
screws and remove its cover.
1
2. Disconnect the ribbon cable between the Rotor
4 5
Board High Speed and the LVPS Board .
2
3
Disconnect cables CF1 and CF2 .
3. Disconnect Capacitor cables CF9, CF10, CF11, CF12
6 4
.
1
4. Unscrew two 5.5 mm hex head screws that are in holes
3
below the surface of the board and that secure an
IGBT.
5. Unscrew the eight 5.5 mm hex head screws and
4 5
remove the Rotor Board High Speed .

Be careful to preserve the special grease

CAUTION
that is spread between the IGBT and a
heat sink under the Rotation Board. This
grease, called ”Conductive Surface
Compound”, provides both thermal and
electrical conductivity that are important 2 6
in reducing failure of the IGBT.

6 REASSEMBLY

Reverse the disassembly procedure to reinstall the Rotor Board High Speed.
Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).

CAUTION Ensure that cables are correctly connected. Ensure that marks on the cables match the
marks on the board.

Remount the cover. Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).

7 VERIFY

Verify that the system functions correctly.

Run Heater Function Diagnostics.

9-79
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 1/3 D/R JEDI 17-46

subassembly: :AEC Board (Option)

purpose: version no. 0
date: 20/12/99
NF No. Production date Serial No. Personnel:1
from / / from Time: 0h 10min
to / / to

1 SUPPLIES

None.

2 TOOLS

5.5 mm nut driver or socket wrench with ratchet.

3 SAFETY PRECAUTIONS

BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF. APPLY
DANGER
LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN MANIPULATING
INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, do not forget to wear the antistatic bracelet.

4 PREREQUISITES

THE WHOLE INVERTER UNIT WEIGHTS 30 KILOGRAMS (66 POUNDS). TWO PEOPLE
WARNING ARE REQUIRED TO CARRY IT.

9-80
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 2/3 D/R JEDI 17-46

5 DISASSEMBLY

The installation of the AEC Board can

NOTICE
be done without removing the
Interface Unit from the Cabinet.

Interface
Unit

5-1 Remove the AEC Board

1. Unscrew twelve 5.5 mm screws that retain the cover

1
panel and remove this one . 1

9-81
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

PROTEUS XR/a 3/3 D/R JEDI 17-46

4
2. Disconnect the flat ribbon cable from J5 between
2 3
the I/F Board RAD and the AEC Board . 4
2
3
6 7
3. Disconnect the connectors J2 and J1 , and Test
5 5
Points TP1 and TP2 on the AEC Board.

4. Remove the six 5.5 mm screws securing the AEC 6

Board 3 .
7

6 REASSEMBLY

Reverse the disassembly procedure. Tighten screws to torque between 1.5 and 2 N.m (15 to 20 kg.cm).

7 VERIFY

Reapply power.
Proceed to ”AEC diagnostics” to ensure correct operation.

9-82
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

CHAPTER 10 SCHEMATICS
SECTION 1 PROTEUS XR/a SYSTEM MIS MAP
1-1 System Schematics (1) (For systems with Wall Stand 2260354)

(For MX100 :2378475)

(For MX100 :2378473)
For MX100 tube: 2380062(rotor)/2380063(thermal)/2269002(HV Cables)/2378816(tube fan)

10-1
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
System Schematics (2) (For systems with SG100 Wall Stand 2225849)

(For MX100 :2378475)

(For MX100 :2378473)
For MX100 tube: 2380062(rotor)/2380063(thermal)/2269002(HV Cables)/2378816(tube fan)

X-ray

2365706

10-2
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
1-2 PDU Schematics

10-3
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
1-3 Wall stand Schematics

10-4
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-4 SG100 Wall stand Schematics (sheet 1 of 2)

10-5
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
SG100 Wall stand Schematics (sheet 2 of 2)

10-6
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-5 SG120 Wall Stand Schematics (sheet 1 of 3)

5 4 3 2 1

2140362-* (MIS 27300-301-302) S0004981 S0005407 S0004979 S0005409 S0005410

CARRO BRAZO SOPORTE TILT. SOPORTE BUCKY. BUCKY.

S0005408
BRAZO - PCB
D D
L1 VERT. BRAKE 1
S4 3
2 B. UPPER
INTERFACE BOARD

GND[1..1]
1
CONTROL BOARD L2 VERT. BRAKE 2

S0005058 S5 3
J6[1..4] 2
1
2410108-* (MIS 27225) S0008838 S0007675 B. LOWER
J1 VAC[1..3] J3 [1..16] J11 [1..16] J7[1..4]

SW1 3
2
1 VERT. MOV.
S0008837
J8[1..2]

SW2-1 3
J13 [1..2]
2
1

SW2-2 3 TILT. MOV.

C 2 C
1
S0004970
J9 [1..4]

L3 TILT. BRAKE 3 S1 3
2
S0004982 1 TILT. VERT.
J12[1..2]
S3 3
2
1
S0007674 TILT. HOR.
J10[1..6]

S0004978
S2-1 3
J14 [1..6]
2
S0007602 1

S2-2 3
2 BUCKY ROT.
1
B B

S0007651 S0007652
JP13 J13 D1 INDIC. ALIMENTACION
J13 [1..2]
1 1
2 2

BUCKY ASSY.
2145641-* (MIS 27221) S0007648
J42 [1..26] J42 [1..26] J4 BUCKY[1..6]

2145644-* (MIS 27223)

J41 [1..15]
2145656-* (MIS 27224)
J45 [1..9] J6 [1..16] J5 SESING[1..14]

A A
2145642-* (MIS 27222)
J40 [1..14] S0007026
J40 [1..14] PL1 ION CH.[1..14]

S0005193 BUCKY
Title
CABLEADO W.S. SG 120
OPCION: J12 ALIMENTACION EN VDC.
Size Document Number Rev
* SEGÚN LONGITUD DE CABLE A3 S0009143SCH
1
Date: Monday, August 02, 2004 Sheet 1 of 1
5 4 3 2 1

10-7
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SG120 Wall Stand Schematics (sheet 2 of 3)

5 4 3 2 1

J6
VERT. BRAKE COIL
1
2
+24V1 3
D 4 D
AMP280371-2

J7
BUCKY UPPER SW.
1
BUCKY LOWER SW. 2
3
4
AMP280371-2
J11
J8
1 VERT. MOVE SW.
2 1
3 0V1 2
4 AMP280370-2
5
6
7
C C
8
9
J9
10 TILT MOVE SW.
11 1
12 +24V1 2
13 3
14 4
15 +24V1
0V1 AMP280371-2
16

AMP280385-2 J12
TILT BRAKE COIL 1
+24V1 2

J13 AMP280370-2

1 +24V1 J10
2 0V1
BUCKY VERT. SW.
1
B B
AMP280370-2 BUCKY HOR. SW. 2
3
4
5
6
AMP280372-2

J14
BUCKY ROT. SW.
1
2
H1 24VDC EXT. 3
4
1 5
H2 6
1 AMP280372-2
H3
A 1 A
H4 SUINSA
1 Title
PWA INTERCONEXIÓN COLORADO
Size Document Number R ev

A4 S0007602SCH 1
Date: Wednesday, May 26, 2004 Sheet 1 of 1
5 4 3 2 1

10-8
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SG120 Wall Stand Schematics (sheet 3 of 3)

5 4 3 2 1

J2 FOR 115Vac F3 MF-R400 J12

----------- J2 FOR 230Vac +24V1
* J2 PARA
115Vca
1 2 3 4 1 2 3 4
-----------
J2 PARA * 1
2

J2 * 230Vca 0V1
3

AMP350210-1 J3

BUCKY UPPER 1

1
2
3
4
AMP350430-1
BUCKY LOW ER 2
VERT. MOVE 3
D1
TILT MOVE 4
D BUCKY VERT. D
FB1002L 5
F2 BUCKY HORIZ. 6
1 T1 5 +24V1 BUCKY ROTATED
BLUE/AZUL BLACK/NEGRO 7
J1 24VDC EXT. 8

1
0,5 A SB C6
VERT. BRAKE 9
470pF 400Vac RV3 F1 MF-R400
L GRAY/GRIS TILT. BRAKE 10
T
V130L10 2 6 RED/ROJO 11
N
DS1 4 8 4 - + 2 D3 + C3 + C4
12
LAMP NEON C8 VIOLET ORANGE/NARANJA
+24V1

2
47nF 250Vca 13
IEC 320 RV2 R5 SMCJ30A 2200uF 50V 2200uF 50V 14
BROWN/MARRON 3 15
V130L10 7 YELLOW/AMARILLO 0V1

3
230Vac +/- 10% 470 ohm 10W 16
R15 C7
50/60 Hz 0V1
270K 470pF 400Vac TRAFO TOROID 50VA AMP280385-2
R6
0 OHM

R7 2K2
J13
+24V1
1 1
2 2 0V1

AMP280370-2
J6
C 1 C
2 +24V1 TILT. BRAKE
3
4 R1
5 PUENTE R2 R3 R4
6 CR2
7 100 ohm 10W
8 S1J
9 C2 100uF 50V
10

+
11

4
Q3 Q1
12 MTD20N06HDL MTD20N06HDL
13 D2 C1 100uF 50V
14

+
15 TILT MOVE 1 1
16 R14 10K R9

3
C9 BAS85 R12 R13 4K7
AMP280385-2 JP1 100nF 2K2 D4 4K7
B BAS85
3 0V1
2
1 A
J41
PUENTE
8 R8 10K
15
7
14 24VDC EXT.
6
13 BUCKY LOW ER
B B
5
12 BUCKY UPPER
4
11 BUCKY ROTATED
3
10 BUCKY HORIZ.
2 +24V1
9 C5
BUCKY VERT.
1 1uF 250v
VERT. BRAKE
AMP 747845-3
CR1

R11 S1J
10K

4
RV1
J45 V130L10
5 Q2
9 1 FQD9N25
VERT. MOVE
4
8 R10

3
3 C10
7 100nF 4K7
2 0V1
6
1
A 21 A
11
AMP 747840-4 1 1
31 41
1 1
51 61
1 1 Title

PWA W. S. CONTROL COLORADO

Size Document Number Rev
A3
S0005193SCH 3
Date: Monday, May 17, 2004 Sheet 1 of 1
5 4 3 2 1

10-9
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-6 SystemI/F Board (1)

1 2 3 4

D D

GAIN = 25MV/CM (TABLE, OCS, SID)

RA11
J110 120 TP1
DB9
+12
5 1-2
9
4
R20
TABLE ELECTRIC

8 TAB_SID_REF_RTN SW-1
R1 L7D 7.5K
3
10K LF444
7 TAB_SID 12 1-1 +12
2 14
6 TAB_SID_REF R5 13
C28

4
1 100K R15
10u 25V P5
10K L7A
+12 5K R18 3 LF444
RA10 1 R7 AI1
C 4.7K C
7.5K PA1 TP2 2 10K
5K R17
R16
10K
10K

11
+12
RA12 L7C
R10
10 LF444
120 PA3 C36 100K
8 -12
0.1u 50V
2K 9 2-1
SW-2
OCS_SID_REF
R3
10K
OCS_SID +12
2-2
OCS_SID_REF_RTN R8
C29
100K R4
10u 25V R85
120
TP3 3-2
0
+12
RA13
SW-3
B 120 L8B B

4
P4 L8A
5 3-1
7 100K R12 3
6 1 R19 AI0
R11 4.7K
2 10K
10K R14
10K

11
R13
C35 10K
-12
0.1u 50V

A A

Date 2004-10-29
Revision 3
Number 1/6

1 2 3 4

10-10
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SystemI/F Board (2)

1 2 3 4

D D

J111 +5
DB25
13
25 +12
12 SID_A
24 SID_B

4
6
8
11 SID_C

(J101)
23 SID_D
10 SID_E
22 DETENT VALID VERT_DETENT_IN D9 RLY
9 DS2E-M
1N4148
21 VERT_DETENT_1
8

2
3
4
5
6
7
8
20 VERT_DETENT_2

16

13
11
9
7 RES5
OCS CONTROL BOARD

19 ORDO_LOCK_RELEASE
C C
6
18 P21V R36 4.7K T1
5 7*10K
17 XT_OK_FOR_TOMO 2N708

1
4
16 OCS_SID_REF_RTN C25
3 10u 25V
15 OCS_SID
2
14 OCS_SID_REF
1
+5

EMI1
104Z
1 3
Vin Vout

GND
RA1 CTA1 CTA2
B B
10M/0.5W 470u/25v 470u/25v

2
+12
D101N4148

J114 VR11
6PIN KA7809A +12
1 3 +9V
Vin +9V
PDU (TM2)

6 CTA4 C37 CTA5

GND

C38
5 C26 100u/25V 0.1u/50V 100u/25V
DC0V 0.1u/50V
4 C27 C10
+12V
3 10u/25V 0.1u 50V
2 0.33u 50V
2

-12V
1
+5V

A A
-12

Date 2004-10-29
Revision 3
Number 2/6

1 2 3 4

10-11
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SystemI/F Board (3)

1 2 3 4 5 6 7 8

D GAIN = 100mV/CM(FILM SIZE) TP7 D

RES6-2 10K L5C
TABLE_CASS_IN +12 +12
LF444 R65
10 AI3 TP8
10K
J112 +5 8

4
DB9 9 L5D
L3A L5A R66
5 TABLE_LAT_SIZE RES7-2 12 LF444
TABLE CASSETTE TRAY
R37 10K LF444 R39 LF444 R57 P10 10K
9 510 3 3 14 AI2
10K 10K 100K
4 1 1 13
8 TABLE_LONG_SIZE 2 2 P11
C13
3 100K
10u 25V R41
7 T_C R61
10K
2 TABLE_VOLT_REF 2K

11

11
R94 100K L3C
6
LF444 R44 L5B
1 TP5 10
-12 +12 10K LF444
-12 -12 8 5
R42
L3B 9 7
P6 R38 10K 10K
5 LF444 6
R32 R40 10K R93
VR9 R31 100K 7 C15 R62 R58
120 100K
9.1V C14 6 2K 10K
120 0.1u 50V 10u 25V TP6
R46
L3D 10K
VR7 VR6 R43 10K LF444 R45
9.1V 12
9.1V 10K
C P7 14 C
R33 100K 13
120 C16
0.1u 50V
TP11
L6C
+12
-12 LF444 R67
+12 10 AI5 TP12
10K
8

4
J113 +5 9 L6D
R68

4
DB9 L6A 12 LF444
R47 L4A R59 10K
WALL CASSETTE TRAY

5 WALL_LAT_SIZE 3 LF444 P12 14 AI4

10K LF444 R49 10K
9 3 1 100K 13
10K
4 1 2
(PROTEUS)

C17 P13
8 WALL_LONG_SIZE 2
10u 25V R51 100K
3
10K
7 R91 R63

11
L4C
2 WALL_VOLT_REF 100k 2K
11
LF444 R54 L6B
6 10
10K LF444
1 TP9 -12 8 5
+12 R52
-12 9 7
R48 10K
L4B 6
10K R50 R60
P8 5 LF444 R92 R64
R34 10K C19 10K
100K 7 100K 2K
120
B C18 6 TP10 B
10u 25V R56
0.1u 50V
J124 L4D 10K
R53 10K LF444 R55
E N 12
P9 10K
R VR8 14
D A 9.1V 100K C20 13
P 0.1u 50V
C M
L
B K
H
F
BUCKY_VERT BUCKY_HORIZ BUCKY_ROTATE BUCKY_UPPER BUCKY_LOWER WALL_CASS_IN

B_V B_H B_R B_U B_L W_C

WALL CASSETTE TRAY
(SG100)
RES6-4 RES6-5 RES6-6 RES6-7 RES6-8 RES6-3
RES7-4 RES7-5 RES7-6 RES7-7 RES7-8 RES7-3
10K 510 10K 510 10K 510 10K 510 10K 510 10K 510

A A

Date 2004-10-29
Revision 3
Number 3/6

1 2 3 4 5 6 7 8

10-12
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SystemI/F Board (4)

1 2 3 4

D D

J115
DB25
CAN_H 1 J118
CAN_L 14 DB9
2 CAN_H 1
15 CAN_L 6
3 2
TOMO_STROKE_START 16 7

JEDI(J9)
4 3
ORDER_RX 17 PREP_SW 8
5 EXP_SW 4
ORDER_RX_RTN 18 9
6 5
P12V 19

TOMO
7
XT_OK_FOR_TOMO 20
C 8 C
ORDO_LOCK_RELEASE 21
9 J119
P21V 22 CAN_H 1
10 CAN_L 9
23 2
11 10
24 J120 PSW 3
12 1 PREP_SW 11
25 2 EXP_SW 4
13 PSW 3 12
DC12V 4 5
5 DC12V 13
6 6
J116
DC12V 14
DB9
6PIN 7
CAN_H 1
DC12V 15
CAN_L 6
8
2
CC2 CC1 7
B 3 DB15 B
22p 50V 22p 50V
8
XT

+9V 4
9
5

J123
DB9 ORDER_RX_RTN
1 ORDER_RX
6 P12V
CAN_L 2
CAN_H 7 TOMO_STROKE_START
3
8
OPTION

4
26
25
24
23
22
21
20
19
18
17
16
15
14
13
12
11
10
9
8
7
6
5
4
3
2
1
9
5
J117
A A
26PIN
JEDI(J1)

Date 2004-10-29
Revision 3
Number 4/6

1 2 3 4

10-13
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SystemI/F Board (5)

1 2 3 4

D D

+5V U1 80C592 U2 74LS373 U3 27256

AD0 3 2 A0 10 11 AD0
D0 Q0 A0 D0
ADC0 1 36 A8 AD1 4 5 A1 9 12 AD1
ADC0 P20 D1 Q1 A1 D1
R79 3 37 A9 AD2 7 6 A2 8 13 AD2
STADC P21 D2 Q2 A2 D2
10K STT 4 38 A10 AD3 8 9 A3 7 15 AD3
PWM0 P22 D3 Q3 A3 D3
5 39 A11 AD4 13 12 A4 6 16 AD4
PWM1 P23 D4 Q4 A4 D4
EW 6 40 A12 AD5 14 15 A5 5 17 AD5
EW P24 D5 Q5 A5 D5
P40 7 41 A13 AD6 17 16 A6 4 18 AD6
P40 P25 D6 Q6 A6 D6
R83 P41 8 42 A14 AD7 18 19 A7 3 19 AD7
P41 P26 D7 Q7 A7 D7
0 P42 9 43 A8 25
P42 P27 A8
P43 10 44 PSEN 1 A9 24
P43 PSEN OE A9
P44 11 45 ALE 11 A10 21
P44 ALE LE A10
P45 12 46 A11 23
P45 EA A11
C P46 13 47 AD7 A12 2 C
P46 P07 A12
P47 14 48 AD6 A13 26
P47 P06 A13
RST 15 49 AD5 +5V A14 27
RST P05 A14
DETENT P10 16 50 AD4
P10CT0 P04
P11 17 51 AD3 PSEN 22
P11CT1 P03 OE
RES3-8 P12 18 52 AD2 20
P12CT2 P02 CE
P13 19 53 AD1 1
P13CT3 P01 VPP
P14 20 54 AD0
P14/T2 P00
P15 21 55 REF
P15RT2 REF
22 56 CRX1
CVSS CRX1
CTX0 23 57 CRX0 C31
CTX0 CRX0
P17 24 58
CTX1 AVREF- 0.1u U5 DS1232
P30 25 59 AVRF
P30RDX AVREF+ ALE 7 1
P31 26 60 +5V ST PBRST
P31TXD AVSS
P32 27 61 +5V
INT0 AVDD 6 2
P33 28 62 RST- TD
INT1 ADC7
P34 29 63 R82
P34/T0 ADC6 RST 5 3
P35 30 64 ADC5 RST+ TOL
P35/T1 ADC5 10K
P36 31 65 ADC4
P36/WR ADC4
P37 32 66 ADC3
P37/RD ADC3 ST
X2 33 67 ADC2
XTAL2 ADC2
B X1 34 68 ADC1 B
M XTAL1 ADC1 STT
C32 20p
16M
U12A TX
CTX0 2 RES4
+5V
C33 20p 3 510*4
1 +5V
U6 82C250 2
3 74LS32 3
VCC CAN_L 1
CTX0 1 4
TXD U12B RX
7 CAN_H 5
CANH 5
CRX1 5
VREF 6
6
CANL CRX0 4
CRX0 4
RXD
2 R80 74LS32
RS

U4 AD584 +12V GND PWR

AVRF R84 2K 1 8 120
V10 VCC
8

2 7
C5 V5 CAP
0.1u 3 6 C34
V2.5 VBG R86
0.1u
A 4 5 0 A
COM STRB

Date 2004-10-29
Revision 3
Number 5/6

1 2 3 4

10-14
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

SystemI/F Board (6)

1 2 3 4

+5V

D D

E5 C8 C9 C23 C12 C11 C21 C22 C24 +5V

22u 0.1u 0.1u 0.1u 0.1u 0.1u 0.1u 0.1u 0.1u

1
RES3
+5V +5V

510*7

D1 D3
+5 RES3-8

2
3
4
5
6
7
8
R74 2K R73 2K

1
AI0 ADC0 AI1 ADC1

SID_A
RES1
U20 TLP521-4 D2 D4
R75 1K E1 C2 E6
SID_A 1 16 C1

SID_B
0.1u
2 15 1K*7 0.1u 10u/25V 10u/25V
SID_B R76 1K 3 14 U21

SID_E
SID_C
4 13 74LS373

2
3
4
5
6
7
8
C SID_C R77 1K 5 12 3 2 P40 C

P21V
SID_D
D0 Q0
6 11 4 5 P41
R78 1K D1 Q1
SID_D 7 10 7 6 P42 +5V +5V
D2 Q2
8 9 8 9 P43
D3 Q3
13 12 P44
D4 Q4
14 15 P45
D5 Q5 D16 D5
U19 TLP521-4 17 16 P46
R30 1K D6 Q6
SID_E 1 16 18 19 P47
D7 Q7 R72 2K R70 2K
2 15 AI4 ADC4 AI2 ADC2
TABLE_CASS_IN R21 1K 3 14 1
OE
4 13 11 D15 D6
R22 1K +5 LE E2 C4 E3
WALL_CASS_IN 5 12 C3
0.1u
6 11 0.1u 10u/25V 10u/25V
P21V R23 2K 7 10
XT_OK_FOR_TOMO 8 9

+5
+5V +5V

1
B B
RES2
U18 TLP521-4 D14 D7
BUCKY_VERT R24 1K 1 16 1K*7
2 15 R71 2K R69 2K
R25 1K AI5 ADC5 AI3 ADC3
BUCKY_HORIZ 3 14 U16
2
3
4
5
6
7
8
4 13 +5 74LS373
D13 D8
5 12 3 2 P10 C6 E7 C7 E8
D0 Q0
P12 6 11 VERT_DETENT_IN 4 5 P11 0.1u 0.1u
R26 1K D1 Q1 10u/25V 10u/25V
BUCKY_ROTATE 7 10 7 6 P13
D2 Q2
8 9 8 9 P14
D3 Q3
13 12 P15
D4 Q4
14 15
D5 Q5
U17 TLP521-4 17 16
R27 1K D6 Q6
BUCKY_UPPER 1 16 18 19
D7 Q7
2 15
R28 1K
BUCKY_LOWER 3 14 1
OE
4 13 11
R29 1K +5 LE
5 12 P21V
+5V
P17 6 11 DETENT_VALID
A A
7 10
8 9

Date 2004-10-29
Revision 3
Number 6/6

1 2 3 4

10-15
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

1-7 Table Schematics

10-16
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Table Logic Control Board (1)

10-17
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Table Logic Control Board (221-3010 for Rev0)

10-18
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Table Logic Control Board (221-3010 for Rev1 & Rev2)

10-19
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
1-8 Pedal I/F Board

10-20
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
1-9 Tomo-link System Schematics
a Cables Illustration

221-3010

10-21
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
b Interconnection.

System Console
TOMO-LINK SYSTEM INTERCONNECTION ILLUSTRATION

REA00057 TOWER
Tomo-Link I/F Board Tomo-Link Main
P1 J105
CAN

VCC TOMO COM J1

8 8
8DEG
21 21 8 DEG J103 CAN BUS inter-

CAN BUS Controller

20DEG 9 20 DEG face Connector

& I/F Circuitry

9 J101

I/O PORTS
40DEG
22 22 40 DEG J2
J104
Sys. I/F

CAN BUS* REA00056

Board

FAST FAST
1,2,14 10 10 J102
SLOW SLOW
*CAN-bus message content: 23 23 OPERATORS

Port 4
• Sweep angle:8,20,40degree; TOMO ON PANEL
•Sweep speed: fast, slow; 2 2
•Tomo ON 3 TOMO RDY
VCC (+5V) 3
•Tomo ready,Tomo start ; +24 TOMO
•Prep. 80C592 6 6 DRIVE UNIT

Isolated
CPU

DC-DC
+24 TOMO
with CAN 7 7
TOMO ON RTN
J102
on chip
15 15
J11 P2 TOMO RDY RTN
J100 J101
1,2,14 I/F Circuitry 16 16
5
Generator

TOMO STROKE PREP

3 19 19
JEDI

3 I/
+12V 6 6 STROKESTART STROKE START
14 14
ORDO RX
4 4 ORDERRX RX EXP
11 11
ORDO RX RTN 5 5 ORDERRXR RX COM
24 24
ORDO LOCKR TOMO LOCK REL Bucky Lock
J101 25 25
Suspensio

12 P21V +21V(XT) Release

12 12 J107 J6
XT

11 XTOK TOMO XT OK FOR TOMO

Table Controller
13 13 1 4
16 +24V SEL TOMO
Sys. I/F 20 20 2 5
Board J3
MOTOR+ 1 1
MOTOR- P3
3 2
10-22 Disable table movement
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
1-10 Tomo I/F Board (1)

10-23
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Tomo I/F Board (2)

10-24
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
SECTION 2
JEDI GENERATOR ILLUSTRATIONS
2-1 JEDI 50PLUS R 1T CABLING
Illustration - Jedi 50Plus R 1T Cabling (1/2)

10-25
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration - Jedi 50Plus R 1T Cabling (2/2)

10-26
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
2-2 JEDI LABELING PLAN

Illustration - Jedi 50 R 1T labeling plan

1 6

2 7
2244165

10-27
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

Illustration - Jedi 80 R 1T labeling plan

10-28
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration - I/F Board RAD V2 Electrical Schematics, Sheet 1

10-15

10-29
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration - I/F Board RAD V2 Electrical Schematics, Sheet 2

10-30
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration - I/F Board RAD V2 Electrical Schematics, Sheet 3

10-31
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration - I/F Board RAD V2 Electrical Schematics, Sheet 4

10-18

10-32
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 1

10-33
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 2

10-34
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 3

10-35
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 4

10-36
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 5

10-37
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 6

10-38
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 7

10-39
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 8

10-40
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet 9

10-41
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet10

10-42
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet11

10-43
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet12

10-44
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet13

10-45
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet14

10-46
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet15

10-47
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet16

10-48
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
Illustration- KV control board _V2C Sheet17

10-49
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
SECTION 3
JEDI GENERATOR CENTRAL LISTING

3-1 kV MEASURE BOARD

CAUTION This board forms part of the oil seal of the High Voltage Tank. It can only be removed at
the factory. The Field Replaceable Unit (FRU) is the complete HV Tank.

LF

C
SF

Illustration - kV Measure Board

10-50
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-2 FILAMENT BOARD 1 INV.

HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR DS3 GOES OUT.
DANGER
DC
160v LF Common
SF

DS3 - Green - +160v

DC present

160v DS4 - Yellow - Inverter

DC Output Running
0

SF_LF - Yellow - Small ON - Yellow - Inverter

Focus / Large Focus Command ON
Relay Feedback
RST - Red - Board being
reset or powered up

DS2 - Yellow - Status

LED

DS1 - Yellow - Status

LED

Illustration - Filament Board 1 Inv.

10-51
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-3 ROTATION BOARD HIGH SPEED

HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR DS6 AND DS7
DANGER
(NEON-ORANGE) GO OUT.

Auxiliary

DC bus Common
Main

DS6

DC bus

Illustration - Rotation Board High Speed

10-52
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-3-1 Indicators

INDICATOR COLOR INDICATES:

RESET Red BOARD BEING RESET OR POWERED UP
INV_ON Yellow THE INVERTER IS RUNNING
DS1 Green PRESENCE OF +15 V SUPPLY
DS2 Green PRESENCE OF -15 V SUPPLY
DS3 Green PRESENCE OF +5 V SUPPLY
DS4-DS5 Yellow BOARD STATUS
DS6 Neon (orange) FAN VAC POWER SUPPLY PRESENT
DS7 Neon (orange) DC BUS PRESENT

3-3-2 J2 Wiring

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16

115V
sense
Fan, 115V AC
Line input
Fan*, 115V AC
Line X-ray tube
Thermal safety

* used in application with fan cooling

10-53
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-4 LV POWER SUPPLY 3 PH BOARD

DANGER
HIGH VOLTAGE AND HOT SURFACE: DO NOT TOUCH BOARD UNTIL INDICATOR NE1
(NEON - ORANGE) GOES OUT.

NE1 - Orange - indicates presence of DC Bus

+ 400

s
- 400

160V
DC
0

DS2 - Green - 160 VDC

DS1 - Red - Mains Drop

Illustration 4 - LV Power Supply 3 Ph Board

10-54
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-5 GATE COMMAND BOARD

DANGER
HIGH VOLTAGE: DO NOT TOUCH BOARD UNTIL DS300 ON THIS BOARD AND DS1 ON
DUAL SNUB BOARD ARE OUT.

CAUTION Hot surface on transformer T300 and heat sink.

D
S3
00

DC bus DS300 - Neon (Orange) -

Presence of voltage on DC
bus for Flyback Converter to
create power supplies for
both Gate Commands

DS200 - Yellow - High

IGBT* (Q200) Gate D
S2
Command running 00

DS202 - Green - Pres ence

DS201 - Green - Presence of -10 V Supply on high
of +20 V Supply on high D D IGBT* Gate Command
IGBT* Gate Command S2 S2
01 02

Inverter ILP
current
feedback
ILR

DS100 -Yellow-Low IGBT*

D
(Q100) Gate Command running S1
00
DS102 - Green - Presence
D
DS101 - Green - Presence of D S1 of -10 V Supply on low
S1 02
+20 V Supply on low IGBT* 01 IGBT* Gate Command
Gate Command

* Insulated Gate
Bipolar Transistor

Illustration - Gate Command Board

10-55
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

6 kV CONTROL BOARD

Illustration - kV Control Board

10-56
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-6-1 Switches and Jumpers

SWITCH OR FUNCTION
JUMPER
RST RESET PUSH BUTTON

3-6-2 Indicators

INDICATOR COLOR INDICATES:

CONF Red FIELD PROGRAMMABLE GATE ARRAY
(FPGA) CONFIGURATION NOT
ACCOMPLISHED
OK Yellow INVERTER GATE POWER SUPPLY OK
TX_TAV Yellow TRANSMIT TO SERVICE LAPTOP
RX_TAV Yellow RECEIVE FROM SERVICE LAPTOP
TX_CONS Yellow TRANSMIT TO CONSOLE (IF EXISTING)
RX_CONS Yellow RECEIVE FROM CONSOLE (IF EXISTING)
T_CAN_X Yellow SYSTEM CAN BUS TRANSMIT
R_CAN_X Yellow SYSTEM CAN BUS RECEIVE
HALT Red MICROPROCESSOR HALTED
RESET Red BOARD BEING RESET
S0 TO S7 Yellow STATUS LED
IN APPLICATION MODE THESE LEDS
FLASH IN SEQUENCE CONTINUOUSLY
DS1 Green -15V SUPPLY
DS2 Green +15V SUPPLY

3-6-3 Non Volatile RAM

REFERENCE DESIGNATION
U32 NON VOLATILE PARAMETERS RAM (BATTERY
INCLUDED)

10-57
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100

3-7 AC/DC 3 PHASE BOARD

DANGER
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL DS1 (NEON - ORANGE) GOES
OUT.

CAUTION Some components on this board can become very hot.

DC Bus to DC Bus out

F1 - Fuse -
DS1 - Neon Protects (on DC Bus):
(Orange) - Indi LV Power Supply 3 Phase Board
cates presence Rotor Board High Speed
of voltage on the Gate Command Board
DC Bus. Type: 15 A, 600 VDC

Illustration - AC/DC 3 Phase Board

10-58
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-8 I/F BOARD RAD V2

ON & VAC N1 - Orange (neon) -

Indicates presence of
Pin 9 100 VAC for the Bucky

Table Bucky

Pin 1
Pin 9
Wall Bucky

Pin 1

To AEC board
Pin 9
Room Door & Light

Pin 1
DS4:CAN TRANSMIT
(yellow)

Service Laptop
DS5:EXT.CAN
TRANSMIT (yellow)
DS6: Receive Data
from console (yellow)

Console
OPTIONAL

DS7: DATA being sent to

console (TRANSMIT) No strap (engineering
(yellow) use)

Presence of strap -
TUBE 1

DS3:Reset led (red)

DS1, DS2: Status micro

processor (yellow)

Illustration - I/F Board RAD V2

10-59
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-9 AEC BOARD V2

AEC4 AEC3 AEC1 AEC2 N1 - Orange (neon) -

Presence of 230 VDC

Illustration - AEC Board V2

3-9-1 Test Points

TESTPOINT MEASUREMENT
SIGNAL RANGE
TP1 230 VDC 230 VDC _5%
TP2 230 VDC 230 VDC _5%
TP3 230 VDC 230 VDC _5%
TP4 230 VDC 230 VDC _5%
TP5 AEC assignment reference 0 to 10 V
TP6 10 VDC (reference) 10 VDC _1%
TP7 AEC return voltage
TP8 AEC1 return voltage
TP9 AEC2 return voltage
TP10 AEC3 return voltage
TP11 AEC4 return voltage

10-60
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
3-10 QUAD SNUB BOARD

DANGER
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR DS1 (NEON -
ORANGE) GOES OUT.

DS1 / DS2 - LED (green) - Indicates presence of voltage on DC Bus

Illustration - Quad Snub Board

10-61
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
SECTION 4 OTS CONSOLE ILLUSTRATIONS
4-1 Release Handle Schematics

SW1
2
1.3
ALL_IN 4

8
5.7
6

SW DPDT

SW2
2
1.3 ALL_OUT
4

8
5.7
ALL_VERT_IN 6
ALL_VERT_OUT
SW DPDT

J6
ALL_IN 1
ALL_VERT_IN 2
ALL_OUT 3
ALL_VERT_OUT 4
CONN_4

Title
ALL LOCK/RELEASE HANDLE
Size Document Number Rev
A
WDS-105-C-001
Date: Saturday, May 27, 2000 Sheet 1 of 1

10-62
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 VCC
DIRECTION 2273022-100
4-2 OTS Console Processor Board -1 R88
10K1%0.1W

U7
1 8
2 NC.1 CATHODE VCC VCC VCC VCC VCC VCC VCC VCC
VCC 3 NC.2
4 NC.3 C34 R132
5 NC.4
6 NC.5 SPARE_rc0805
R149 7 NC.6 4 R61 R60 R59 R58 R57 R56 R55 R46
NC.7 ANODE
10K1%0.1W 0.1uF50V SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805
U1D LM285-2.5
R5 R22 100 1%0.1W
9 8
SWITCH16
100K1%0.1W C1 VCC
74HC14

R150
0.1uF50V 10K1%0.1W

U1C R35
R19
VCC 5 6
SWITCH17
R49 R48 R47 R52 R51 R50 R54 R53
100K1%0.1W
R151 1001%0.1W SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805
74HC14
10K1%0.1W C4
0.1uF50V
U1A
R14 R34
1 2
SWITCH18 these pulldowns should not exceed 8k
100K1%0.1W 100 1%0.1W
74HC14 VCC
C9
0.1uF50V
R152
10K1%0.1W

U1B R23 VCC VCC VCC

R20
VCC 3 4
SWITCH19
100K1%0.1W R168 R169
R153 74HC14 100 1%0.1W 1K150.1W 1K1%0.1W
10K1%0.1W C10
0.1uF50V
U3D U8
R15 R31 R189 R183 3 1
+5V PWM PWM_INC
9 8
SWITCH20
7 6
RX TXEN TXEN_INC
100K1%0.1W 100 1%0.1W VCC
74HC14 VCC 2
C5 SPARE-RC0805 100 1%0.1W C37 5 NC-2
0.1uF50V 0.1uF50V NC-5 8
R154 4 TX
GND
10K1%0.1W (7,21,40,53,61) VDD
SG104001 VCC

U3E R182
R6 R32
11 10 U6
SWITCH21
VCC 40 R165
100K150.1W 100 1%0.1W VDD 8 100 1%0.1W 10K150.1W
VAREF 1 P3.4/T3EUD 9
74HC14 LED_I U3F
R155 C6 28 Varef P3.6/T3IN 10
VPP VPP/_EA P3.6/T3IN _ENABLE_LED R28 R11
10K150.1W 0.1uF50V 11
P3.9/MTSR P3.9
MUX_SIG0 37 12 KEYSW_DB 12 13
POH.0/AD8 P3.10/TXD0 TXD KEYSW
U3B R24 MUX_SIG1 38 13
POH.1/AD9 P3.11/RXD0 RXD
R8 MUX_SIG2 39 14 100K1%0.1W
POH.2/AD10 P3.12/_BHE/_WRH P3.12
3 4 MUX_SIG3 42 15 100 150.1W
SWITCH23 POH.3/AD11 P3.13/SCLK P3.13
MUX_SIG4 43 16 74HC14 C26
POH.4/AD12 P3.15/CLKOUT P3.15 0.1uF50V
100K1%0.1W 100 1%0.1W MUX_SIG5 44 VCC VCC
45 POH.5/AD13 17 VCC
74HC14 MUX_SIG6 P4.0
C11 VCC 46 POH.6/AD14 P4.0/A16_CS3 18 R42
DE10_DB MUX_SIG7 POH.7/AD15 P4.1/A17/_CS2 P4.1 CAN_RXD
0.1uF50V 19 SPARE
SW9_DB P4.2/A18/_CS1 P4.2 CAN_TXD
SW8_DB MUS_SELECT0 29 22 R39 FB2 R166 R97
POL.0/AD0 P4.3/A19/_CS0 P4.3 4.99K150.1W 4.99K1%0.1W
R156 SW22_DB MUS_SELECT1 30 23 U4 C19
10K150.1W 31 POL.1/AD1 P4.5/A20/CAN_RXD 24 1 3 0.1uF50V
SW23_DB MUS_SELECT2 POL.2/AD2 P4.6/A21/CAN_TXD TXD VCC CAN+
SW21_DB MUS_SELECT3 32 _NMI VPP
33 POL.3/AD3 76 100 1%0.1W 8 7 BLM21A601S
U3C R33 SW20_DB P0L.4 V5REF
VCC R17 34 POL.4/AD4 P5.0/AN0 77 RS CANH L1
SW19_DB P0L.5 POL.5/AD5 P5.1/AN1 V21REF FB1
5 6 SW18_DB P0L.6 35 78 R41 4 6
SWITCH22 POL.6/AD6 P5.2/AN2 P5.2 RXD CANL PLM3216K281SJ2
SW17_DB P0L.7 36 79 475150.1W
POL.7/AD7 P5.3/AN3 P5.3 _ST CAN-
R157 100K150.1W 100 1%0.1W 2 2 5 VCC
SW16_DB P5.4/AN4/T2EUD P5.4 _RSTIN GND VREF
10K1%0.1W 74HC14 59 3 BLM21A601S
P1H.0/_CC6POS0/EX0IN P5.5/AN5/T4EUD P5.5
C12 62 4 PCA82C250
0.1uF50V P1H.1/_CC6POS1/EX1IN P5.6/AN6/T2IN P5.6
63 5 R40 R44
P1H.2/_CC6POS2/EX2IN P5.7/AN7/T4IN P5.7
U2C R25 64 R184 SPARE
R7 65 P1H.3/EX3IN/T7IN 72
5 6 66 P1H.4/CC24IO P8.0/CC16IO 73
SWITCH8 P1H.5/CC25IO P8.1/CC17IO LED_ELASH
67 74 100 1%0.1W 100 150.1W C50 C29 C31 C28 C30 +21V
P1H.6/CC26IO P8.2/CC18IO PWM_INC 0.01uF50V 0.01uF50V
100K150.1W 100 1%0.1W 68 75 0.01uF50V 0.01uF50V 0.01uf50V VCC
P1H.7/CC27IO P8.3/CC19IO TXEN_INC
74HC14 VCC DN1
C3 47 71 BAT54S
0.1uF50V P1L.0/CC60 _NMI _NMI
48 69
R158 49 P1L.1/COUT60 _RSTIN 70 R91 1
P1L.2/CC61 _RSTOUT _RSTOUT
10K1%0.1W 50 25 VCC 100K1%0.1W R90
P1L.3/COUT61 _RD _RD ? 10K1%0.1W
51 26 U5
P1L.4/CC62 _WR_WRL _WR
U2D R29 52 27 _PBRST 2 15
P1L.5/COUT62 ALE ALE _RESET VCC
R16 57 13
VCC 9 8 58 P1L.6/COUT63 VCC 6 _ST 11 D7
SWITCH9 P1L.7/_CTRAP TOL _RST V21REF V5REF
SW15_DB 55 VCC 4 9 C25 R89
XTAL1 XTAL1 TD RST RST_WD 0.1uF50V UTP5 5V
100K150.1W 100 1%0.1W SW14_DB VSS (6,20,41,56,60) 80 10K1%0.1W
R159 VAGND R4 VCC 16 R98 C36
74HC14 SW13_DB
10K1%0.1W C2 60 54 R173 1 NC-16 14 C35 4.99K150.1W 0.1uF50V
SW12_DB VSS XTAL2 NC-1 NC-14
0.1uF50V R43 3 12 0.1uF50V
SW11_DB 1K1%0.1W NC-3 NC-12
U2B 1.00Meg1% SPARE 5 10
R13 R30 R45 7 NC-5 NC-10
C164CI SPARE NC-7
3 4 8
SWITCH10 U9 GND
Y1
100K1%0.1W 100 150.1W R1 10 MHz DS1232
74HC14 VCC XTAL2 3 1
C8 VCC OSC EN R171
0.1uF50V 0 1K1%0.1W
10 MHz R170
R160 C32 C33 1K150.1W
10K150.1W + C27 C51 C52 C53 C54 18pf50V 10pf50V
47uF16V 0.01uF50V 0.01uF50V 0.01uF50V 0.01uF50V
U2A R26
R21 VCC
VCC 1 2
SWITCH11
100K150.1W 100 1%0.1W place caps near microcontroller
R161 74HC14
10K1%0.1W C7
0.1uF50V R77 R175 R79 R66 R67 R68 R69 R70 R71 R176 R177 R82 R83 R72 R73 R74 R75 R178 R179 R180
U2E R36
R18 10K1%0.1W SPARE_rc0805 10K150.1W 10K1%0.1W 10K150.1W 10K150.1W 10K150.1W 10K150.1W 10K150.1W SPARE_rc0805 SPARE_rc0805 10K1%0.1W 10K1%0.1W 10K1%0.1W 10K1%0.1W 10K1%0.1W 10K1%0.1W SPARE_rc0805 SPARE_rc0805 SPARE_rc0805
11 10
SWITCH12
100K1%0.1W 100 150.1W P3.15
P3.8
74HC14
C17 VCC P3.9
0.1uF50V P3.12
P3.13
R162 P4.0
10K1%0.1W P4.1
P4.2
P4.3
U2F
R10 R27 P5.0
13 12 P5.1
SWITCH13 P5.2
VCC
100K1%0.1W 100 150.1W P5.3
P5.4
74HC14
R163 C18 P5.5
10K1%0.1W 0.1uF50V P5.6
P5.7
P8.1
U1E R37
R9 P8.2
11 10 P8.3
SWITCH14
100K1%0.1W R112 R113 R114 R115 R116 R117 R118 R119 R120 R121 R122 R123 R124 R125 R126 R127 R128 R129 R130 R131
74HC14 100 1%0.1W
C23 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805
0.1uF50V VCC

R164
10K150.1W
VCC VCC VCC VCC VCC VCC VCC VCC
U1F R38
R12
13 12
SWITCH15
100K1%0.1W 100 150.1W R137 R136 R135 R134 R133 R148 R147 R138
C24 74HC14
0.1uF50V SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805

MUX_SELECT0
MUX_SELECT1
MUX_SELECT2
MUX_SELECT3
POL.4
VCC POL.5
U3A POL.6
R172 POL.7
1 2
TP17
R141 R140 R139 R144 R143 R142 R146 R145
1K1%0.1W C20 C21 C22
0.1uF50V 0.1uF50V 0.1uF50V SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 SPARE_rc0805 Title
74HC14

spare GE MEDICAL
Size Document Number Rev
D 1.0
place caps near schmitt triggers OCS CONSOLE PROCRSSOR BOARD
these pulldowns should not exceed 8k Date: Tuesday, February 06, 2001 Sheet 1 of 2

10-63
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
4-3 OTS Console Processor Board -2 VCC

C45
VCC 0.1uF50V

+21V
ALL LOCK/RELEASE LONG TRANS
J4 FB3 FB4
SW3 SW4 SW5
SWIICH8 1 2
3 4 SWIICH9 ALL_INH LONG_SIG TRANS_SIG
SWIICH10 ALL_OUTH
5 6 SWIICH11 ALL_OUTH
SWIICH12 BLM21A601S
7 8 SWIICH13 VERT_SIG
SWIICH14 VCC VCC VCC BLM21A601S
9 10 SWIICH15
SWIICH16
11 12 SWIICH17
SWIICH18
13 14 SWIICH19
SWIICH20
15 16 SWIICH21
SWIICH23
17 18 SWIICH22
SW DPDT SW DPDT SW DPDT
19 20
CONN_20
R101 R102 R104
474 1% 0.1W 475 1% 0.1W 475 15 0.1W
VCC J2
LONG_SIG
R93 R95 TRANS_SIG 1
C38 C39 100K 1% 0.1W C41 100K 1% 0.1W DET_SIG 2
C44 VCC 0.1uF50V 0.1uF50V 0.1uF50V V_SIG 3
0.1uF50V D1 D2 D4 ANGLE_SIG 4
5
HLMP-15-1540 HLMP_1540 HLMP_1540 TP1 6
TP8 7
J5
TP9 8
RST_WD 1 2 TP10 9
MUX_SELECT0 3 4 _ENABLE_LED TP11 10
MUX_SELECT2 5 6 MUX_SELECT1 TP12 11
7 8 MUX_SELECT3 12
MUX_SIG0
MUX_SIG2 9 10 MUX_SIG1 THESE COMPONENTS WILL BE 13
MUX_SIG4 11
13
12
14
MUX_SIG3
MUX_SIG5
LOCATED ON A SEPARATE PCB 14
15
MUX_SIG6
LED_FLASA 15 16 MUX_SIG7 IN THE CONSOLE"S HANDLE" 16
17 18 LED_I 17
19 20 18
TP2 19
CONN_20
TP3 20
SW1
TP4 21
+21V TP5 22
TP6 23
24
25
C47 CONN_25
ALL_OUT R181
0.1uF50V
ALL_IN SW DPDT

SW2 VCC L2 SPARE_RC0805 +5V

FB8

4.7uH HI18127800R

+ C55 C49 C48

100uF 16V 0.1uF50V 0.1uF50V
ALL_VERT_IN
ALL_VERT_OUT
SW DPDT

J6 R174
ALL_IN 1
ALL_VERT_IN 2
ALL_OUT 3 SPARE_RC0805
ALL_VERT_OUT 4
J1
CONN_4 CAN+
CAN- 1
2
TP7 3
U6-2
VAREF TP13 4
P5.5 1 2 P5.4 TP14 5
3 4 P5.6 R167 6
P5.7
VDD 5 6 VSS 7
LED_I 7 8 KEYSW_DB 0_OHM 8
P3.9 9 10 _ENABLE_LED 9
RXD 11 12 TXD 10
P3.13 13 14 P3.12 TP15 11
P4.0 15 16 P3.15 TP16 12
P4.2 17 18 P4.1 13
19 20 VSS 14
15
CONN_20
PD5 CONN_15
PD7
PD6
U6-3 PD9
VDD
CAN_RXD 1 2 P4.3 +21V
VERT +21V
DETENT +21V
ANGLE PD8
PD2
3 4 CAN_TXD VERT_SIG
RD PD1 +21V
ALE 5 6 WR PD4
SW6 SW7 SW8
MUX_SELECI0 7 8 VPP PD3
9 10 MUX_SELECI1 FB5 FB6 FB7
MUX_SELECI2
POL.4 11 12 MUX_SELECI3
13 14 POL.5 V_SIG DET_SIG ANGLE_SIG
POL.6 VCC VCC VCC C46
MUX_SIG0 15 16 POL.7 0.1uF50V
MUX-SIG2 17 18 MUX_SIG1 BLM21A601S BLM21A601S BLM21A601S
19 20 VDD
CONN_20 J3
SW DPDT SW DPDT SW DPDT ALL_INH
1
ALL_OUTH 2
R103 R106 R105 VERT_SIG 3
U6-4
VSS 475 1% 0.1W 475 1% 0.1W 475 1% 0.1W 4
MUX_SIG4 1 2 MUX_SIG3
CONN_4
MUX_SUG6 3 4 MUX_SIG5
SW8_DB 5 6 MUX_SIG7 R92 R94 R96
SW10_DB 7 8 SW9_DB C40 100K 1% 0.1W C43 100K 1% 0.1W C42 100K 1% 0.1W
SW12_DB 9 10 SW11_DB 0.1uF50V 0.1uF50V 0.1uF50V
VDD 11 12 SW13_DB D3 D6 D5
XTAL1 13 14 XTAL2
J7
SW14_DB 15 16 VSS HLMP-1540 HLMP-1540 HLMP-1540 _PBRST
SW16_DB 17 18 SW15_DB 1
19 20 VSS 2
CONN_20 CONN_2

JU6-5
VDD
SW18_DB 1 2 SW17_DB
J8
SW20_DB 3 4 SW19_DB KEYSW
SW23_DB 5 6 SW21_DB 1
_RSTIN 7 8 SW22_DB 2
_NMI 9 10 _RSTOUT
CONN_2
LED_FLASH 11 12 _ST
TXEN_INC 13 14 PWM_INC
V2IREF 15 16 V5REF
P5.3 17 18 P5.2
19 20 VSS
CONN_20

Title
GE MEDICAL
Size Document Number Rev
C OCS CONSOLE PROCESSOR BOARD 1.0

Date: Tuesday, February 06, 2001 Sheet 2 of 2

10-64
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
4-4 OTS Console Display Board -1
VCC
VCC VCC VCC VCC
VCC

VCC VCC VCC VCC

R37 R41 R45 R49 C1
100K1%0.1W 100K1%0.1W 100K1%0.1W 100K1%0.1W R131 0.1uF50V

R7 R11 R15 R19 1K1%0.1W

Q24 C10 Q25 C9 Q26 C14 Q28 C12 U9D U9C U9B
FDV304P 0.1uF50V FDV304P 0.1uF50V FDV304P 0.1uF50V FDV304P 0.1uF50V U1 24 12 8 5
R6 100 1%0.1W R10 100 1%0.1W R14 100 1%0.1W R18 100 1%0.1W 2 11 11 10 4
MUX0 D1 S0 KV_LS TP4 TP3 TP2
Q5 Q7 Q9 Q11 3 9 13 9 6
MUX_SIG6 FDV303N MUX_SIG4 FDV303N MUX_SIG2 FDV303N MUX_SIG0 FDV303N MUX1 D2 S1 KV_MID
21 10
MUX2 D3 S2 KV_MS
100 1%0.1W 100 1%0.1W 100 1%0.1W 100 1%0.1W 22 8 14081 14081 14081
MUX3 D4 S3 MA_LS
7 VCC
S4 MA_MID
R38 R42 R46 R50 1 6
ST S5 MA_MS
100K1%0.1W 100K1%0.1W 100K1%0.1W 100K1%0.1W 23 5 R139 R138 R137 R136 R135 R134
INH S6 SID_LS 1K1%0.1W 1K1%0.1W 1K1%0.1W 1K1%0.1W 1K1%0.1W 1K1%0.1W
4
S7 SID_MID
R132 18
S8 SID_MS
17 C23
1K1%0.1W S9 ANGLE_LS 0.1uF50V
20
S10 ANGLE_MID
19
S11 ANGLE_OVER
14
S12 LED_GROUP1
VCC VCC VCC VCC 13
12 S13 LED_GROUP2
S14
16
LED_GROUP3 place Near AND gates
15
S15 TP1
VCC VCC VCC VCC
R35 R39 R43 R47 74HC4514
100K1%0.1W 100K1%0.1W 100K1%0.1W 100K1%0.1W

R5 R9 R13 R17
Q31 C11 Q30 C16 Q27 C15 Q29 C13
FDV304P 0.1uF50V FDV304P 0.1uF50V FDV304P 0.1uF50V FDV304P 0.1uF50V
R4 100 1%0.1W R8 100 1%0.1W R12 100 1%0.1W R16 100 1%0.1W
Q4 Q6 Q8 Q10
MUX_SIG7 FDV303N MUX_SIG5 FDV303N MUX_SIG3 FDV303N MUX_SIG1 FDV303N R63 R64 R65 R66 R67 R68 R69 R70
100 1%0.1W 100 1%0.1W 100 1%0.1W 100 1%0.1W 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1%

R36 R40 R44 R48

100K1%0.1W 100K1%0.1W 100K1%0.1W 100K1%0.1W

D36 D35 D34 D33 D11 D10 D9 D8

VCC
HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540

+ C3 + C2 + C4 + C5 + C6
100uF16V 100uF16V 100uF16V 100uF16V 100uF16V
R1
Q1
LED_GROUP1 FDV303N
100
R32

100K
PROT

R91 R90 R89 R88 R87 R86 R85 R84 R107 R106 R105 R104 R103 R102 R101 R100
20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% KV DISPLAY 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% U2B
U4 ANGLE DISPLAY
11 12 11 13
7 A CATHODE_1 9 10 A CATHODE
4 B CATHOED_2 8 8 B
2 C CATHODE_3 R20 R21 R22 6 C
1 D Q12 Q13 Q14 5 D
E KV_LS FDV303N KV_MID FDV303N KV_MS FDV303N E
10 12
5 F 100 100 100 7 F
G R51 R52 R53 G
3 100K 9
DP 100K 100K DP R71 R72 R73 R74 R75 R76 R77 R78
LTC-571G LTD-6440G 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1%
PROT PROT PROT

R24
Q16
ANGLE_LS FDV303N D39 D40 D38 D37 D15 D14 D13 D12
100
R55 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540

100K
PROT
R99 R98 R97 R96 R95 R94 R93 R92 R115 R114 R113 R112 R111 R110 R109 R108
20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% mAs DISPLAY 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% U2A
U5 ANGLE DISPLAY
11 12 16 14 R2
7 A CATHODE_1 9 15 A CATHODE
4 B CATHOED_2 8 3 B Q2
C CATHODE_3 R23 C LED_GROUP2
2 R27 R26 2 FDV303N
1 D Q18 Q19 Q15 1 D 100
E MA_LS FDV303N MA_MID FDV303N MA_MS FDV303N E
10 18 R34
5 F 100 100 17 F 100K
G R57 R58 100 R54 G
3 100K 100K 4
DP 100K DP PROT
U9A R143
LTC-571G LTD-6440G 1
PROT PROT PROT LED_GROUP2
3 Q34
2 FDV303N
LED_FLASH
R25 100
14081 R148
Q17 100K
ANGLE_MID FDV303N
PROT
100 R56

R123 R122 R121 R120 R119 R118 R117 R116 R128 R127 R126 R125 R124 100K
20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% 20 1% SID DISPLAY 20 1% 20 1% 20 1% 20 1% 20 1%
PROT
U6 U3
11 12 6 4
7 A CATHODE_1 9 3 B CAT_B/C/DP 7
4 B CATHOED_2 8 9 C CAT_B/C/DP
2 C CATHODE_3 R28 R29 R30 1 +
D -
1
E SID_LS
Q20
SID_MID
Q21
SID_MS
Q22
CAT_+/-
2 ANGLE DISPLAY
10 FDV303N FDV303N FDV303N 5 8
5 F 100 100 100 DP CAT_+/- R79 R81 R83 R82 R80
G R59 R60 R61 20 1% 20 1% 20 1% 20 1% 20 1%
LTS-6495G
3 100K 100K 100K
DP
LTC-571G R31
PROT PROT PROT
Q23
ANGLE_OVER FDV303N D18 D19 D20 D17 D16
100
R62 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540 HLMP-1540
100K

PROT
VCC VCC VCC

R146 100K
PROT R3
R149 R145 Q3
VCC LED_GROUP3 FDV303N
100K 100K VCC 100
R140 R33

R144 Q35-1 Q35-2 C7 100K

IRF7301 IRF7301 0.1uF50V U7A
100K U7B PROT
4

R130 R129 LMC6482A

4

R142 R141 100 2 -

6 - R133 1K 1%0.1W 1
Q33 Q32 7 3 LED_I
ENABLE_LED
+
FDV303N RST_WD FDV303N 1K 1K 5 +
100 LMC6482A
100 R150
8

C24 VCC
8

0.5 1% 0.5W 0.1uF50V

FET_OFF
R151 R147
10K 1%0.1W
U8 100K
1 8
2 NC.1 CATHODE
3 NC.2 Title
NC.3
4
5 NC.4 C8
R152
GE MEDICAL
6 NC.5 0.1uF50V SPARE Size Document Number Rev
NC.6
7
NC.7 ANODE
4 D
OCS CONSOLE DISPLAY BOARD 1.0

LM285-2.5 Date: Thursday, June 08, 2000 Sheet 1 of 2

10-65
 PROTEUS XR/a
GE MEDICAL SYSTEMS Service Manual
REV 19 DIRECTION 2273022-100
4-5 OTS Console Display Board –2
VCC

C17
0.1uF50V

VCC

SW8 SW16 J4
1 2
SWITCH8 3 4 SWITCH9
KSIOM410 VCC KSIOM410
SWITCH10 5 6 SWITCH11
SWITCH12 7 8 SWITCH13
SWITCH14 9 10 SWITCH15
SWITCH16 11 12 SWITCH17
SWITCH8 SWITCH16 SWITCH18 13 14 SWITCH19
C19
0.1uF50V SWITCH20 15 16 SWITCH21
SWITCH23 17 18 SWITCH22
19 20
SW9 SW17 CONN_20

KSIOM410 KSIOM410

SWITCH9 SWITCH17
VCC

SW10 SW18 VCC

C18
KSIOM410 VCC KSIOM410 0.1uF50V

SWITCH10 SWITCH18 J5
C20
0.1uF50V 1 2
RST_WD 3 4 ENABLE_LED
MUX0 5 6 MUX1
MUX2 7 8 MUX3
SW11 SW19
MUX_SIG0 9 10 MUX_SIG1
MUX_SIG2 11 12 MUX_SIG3
MUX_SIG4 13 14 MUX_SIG5
KSIOM410 KSIOM410 MUX_SIG6 15 16 MUX_SIG7
LED_FLASH 17 18 LED_I
19 20

SWITCH11 SWITCH19 CONN_20

SW12 SW20

VCC
KSIOM410 KSIOM410

C21 J3
SWITCH12 0.1uF50V SWITCH20
1
FET_OFF 1
2
2
SW13 SW21 CONN2

KSIOM410 KSIOM410

SWITCH13 SWITCH21

SW14 SW23

KSIOM410 KSIOM410
VCC

SWITCH14 SWITCH23
C22
0.1uF50V

SW15 SW22

KSIOM410 KSIOM410

Title
SWITCH15 SWITCH22
GE MEDICAL
Size Document Number Rev
C
OCS CONSOLE DISPLAY BOARD 1.0

Date: Thursday, June 08, 2000 Sheet 2 of 2

10-66