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PLD8000 User Manual-V2.0

This document is the user's manual for the PLD8000 High Frequency Digital Diagnostic X-Ray System. It provides safety and operating instructions, technical specifications, and environmental requirements for the system. Key details include that the system has class I type B electric shock protection and is for continuous operation with intermittent loading. The manual instructs users to read all safety precautions carefully before operation and provides labeling symbols used on the equipment.
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© © All Rights Reserved
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0% found this document useful (0 votes)
330 views128 pages

PLD8000 User Manual-V2.0

This document is the user's manual for the PLD8000 High Frequency Digital Diagnostic X-Ray System. It provides safety and operating instructions, technical specifications, and environmental requirements for the system. Key details include that the system has class I type B electric shock protection and is for continuous operation with intermittent loading. The manual instructs users to read all safety precautions carefully before operation and provides labeling symbols used on the equipment.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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PLD8000 User’s Manual

JS-8000-13 V ER2.0

PLD8000 High Frequency Digital


Diagnostic X-Ray System

User’s Manual

Nanjing Perlove Medical Equipment Co., Ltd.


PLD8000User’s Manual

JS-8000-13 V ER2.0

Medical Device Manufacturing Enterprise License No.: GDFDA20061257

Medical Device registration No.: SFDA(Z) 20142300495

Product standard No.: YZB/S 0113-2014

Electrical equipment security type: This product is a kind of permanently mounted common
equipment with Class I Type B electric shock protection.
The working system is continuous operation with intermittent loading.

The manufacturer will be liable for security, reliability and performance of the equipment
under the following circumstances:
 Assembling, adjustment, operation and maintenance are carry out by authorized
personnel;
 Electric utilities in the room are complying with related provisions;
 The equipment is operated in accordance with user’s manual.

Packaging, storage and transportation requirements:


The product shall be packaged, stored and transported as per the provisions of YY/T
1099-2007 Packaging, Transportation and Storage for Medical X-ray Equipment.
The packaged products shall be adapted to transportation by air, rail, ship and tertiary
highways.
The products shall be stored in:
1) Temperature: -20℃~65℃
2) Relative humidity: ≤93%
3) Atmospheric pressure: 50kPa~106kPa
4) Indoor environment with no corrosive gas
5) Articles exceeding 30kg shall not be stacked on the packing case.

Perlong Medical: Nanjing Perlove Medical Equipment Co.,Ltd.


Add: No. 8877 Zhuhai Avenue, Pingsha Town, Jinwan District, Zhuhai City ,China
Tel: 0756-6235908
Fax: 0756-6235958
Postcode:519090
PLD8000User’s Manual

JS-8000-13 V ER2.0

E-mail: [email protected]
Dear customer:

Firstly, we would express our gratitude to you and your company to select our products!

Before operating the equipment, please make sure to carefully read the Product Manual,

especially the following safety precautions, for you to operate this equipment correctly.

● Please carefully read the following precautions for correct operation of the equipments.

● Before using the equipment, please make sure to get fully known about the performance

and operation of it.

● Pay attention to the following matters for setup and storage place of the equipment:

 No using or storing in place with inflammables and explosives;

 No using or storing in place temperature, humidity and pressure exceeding permitted

ranges;

 No using or storing in place easy to be dampened;

 Avoid tilt, shake and shock (including transportation);

 Pay attention to power supply frequency and voltage as well as allowable current;

 Keep ventilation and avoid direct sunlight.

● Pay attention to the following matters before using the equipment:

 Electromagnetic emission and electromagnetic immunity of the equipment shall meet

requirements specified in YY0505-2012(idt IEC 60601).The equipment may be

operated under typical health care environment specified in YY0505-2012(idt IEC

60601);

 Confirm power supply connection with the equipment and check if the equipment

operates normally;

 Confirm well grounding of the equipment;

 Reconfirm the power supply voltage.


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 In case of equipment failure, instead of disassembling, please paste a note written with

“Break down!” on the equipment, and the Company will assign authorized personnel

for trouble removal.

● No refitting the equipment.

● Maintenance and inspection:

 Regular inspection the equipment and components;

 Before reusing the equipment after a long time out of service, please make sure to

confirm if the equipment can operate normally and safely.

The following advisory symbols will be used throughout this manual. Their application and

meaning are described below.

DANGERS ADVISE OF CONDITIONS OR SITUATIONS THAT IF NOT HEEDED

WILL CAUSE DEATH OR SERIOUS PERSONAL INJURY, AND COULD CAUSE

PART OR ALL OF DAMAGE OF THE EQUIPMENT.

ADVISE OF CONDITIONS OR SITUATIONS THAT IF NOT HEEDED COULD

CAUSE PERSONAL INJURY, OR DAMAGE OF EQUIPMENT OR DATA.

Advise of conditions or situations that if not heeded could


cause misoperation and error action.

The following Security identity symbols will be used the equipment. Their meaning are

described below.

Note, refer to random file

Ionizing radiation
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Type-B equipment

Dangerous voltage

GND

The symbol of electrical equipment and electronic equipment

waste cannot be like without the classification of urban wastes

disposal, shall be handled respectively. Please with the agency

authorized by the manufacturer or authorized waste

management company, access to relevant information about

disposal equipment.

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TABLE OF CONTENTS
CHAPTER1 OVERVIEW....................................................................................................... 1

1.1 Use of the equipment.................................................................................................... 1

1.2 Main structure and feature of the equipment................................................................ 1

1.3 Standards and specifications......................................................................................... 3

1.4 Quality Assurance......................................................................................................... 4

1.4.1 Responsibilities of manufacturer....................................................................... 4

1.4.2 Three guarantees................................................................................................ 5

1.5 Attentions for Safe Operation....................................................................................... 5

1.5.1 General rules...................................................................................................... 5

1.5.2 Electric safety.....................................................................................................6

1.5.3 X-ray safety protection...................................................................................... 6

1.5.4 The effective occupation.................................................................................... 7

1.5.5 Environmental risks and treatment.................................................................... 8

1.5.6 Retirement of equipment....................................................................................8

1.6 Use logo identity........................................................................................................... 8

1.6.1 External label..................................................................................................... 9

1.6.2 Equipment nameplate location.........................................................................12

1.7 ENVIRONMENTAL SPECIFICATIONS.................................................................. 13

1.7.1 The room requirements and Layouts............................................................ 13

1.7.2 Electrical requirements.................................................................................... 14

1.7.3 Environmental conditions................................................................................ 15

CHAPTER2 TECHNICAL PARAMETERS.........................................................................16

2.1 X-ray high voltage generator...................................................................................... 16

2.2 X-ray tube assembly................................................................................................... 16


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2.3 Collimator................................................................................................................... 21

2.4 Radiographic table...................................................................................................... 22

2.5 Flat-panel detector...................................................................................................... 22

2.6 Loading Factor Combination...................................................................................... 22

2.7 Earth leakage current.................................................................................................. 25

CHAPTER3 SYMBOLS DESCRIPTION ON EQUIPMENT..............................................26

3.1 Symbols description on X-ray Generator operation panel..........................................26

3.1.1 Power and exposure control.............................................................................26

3.1.2 X-ray radiography control and display............................................................ 28

3.1.3 Field Select Buttons and Indicators (for AEC only)........................................ 29

3.1.4 Density / ms / mAs up / down buttons and display..........................................31

3.1.5 Setting AEC backup ms or mAs (applies to non CM-thickness mode only)...33

3.1.6 Anatomical programming controls and display............................................... 36

3.2 Symbols description on operation panel of remote console....................................... 39

3.3 Symbols description on local control operation panel of table...................................41

CHAPTER4 INSTALLATION OF THE EQUIPMENT....................................................... 42

4.1 Overview.....................................................................................................................42

4.2 Installation of radiographic table............................................................................. 42

4.2.1 Positioning of the fixed bed base..................................................................... 42

4.2.2 Column components installed..........................................................................43

4.2.3 Tube - limit the installation of beam combination...........................................44

4.2.4 Flat-panel detector, ionization chamber, the installation of filter wire grid.... 46

4.2.5 After the decorative shell installation (the machine debugging)..................... 48

4.3 Equipment cable connection.................................................................................... 48

4.3.1 Power cable and the protection of ground wire............................................... 48

4.3.2 High voltage generator cable connection.........................................................50

4.3.3 Photography bed cable connection.................................................................. 55

4.3.4 Image system cable connection....................................................................... 57


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4.4 Final validation........................................................................................................... 58

CHAPTER5 OPERATION OF THE EQUIPMENT............................................................. 60

5.1 Photography debugging of the bed............................................................................. 60

5.1.1 Photography bed up debugging....................................................................... 61

5.1.2 Ball tube pillar longitudinal motion debugging............................................... 63

5.1.3 Debug the bed surface of lateral movement.................................................... 64

5.1.4 Ball tube mast swing debugging...................................................................... 65

5.1.5 The tube in a sport debugging..........................................................................67

5.2 Use of the equipment—General radioscopy/spot film mode......................................68

5.2.1 General radiography.........................................................................................68

5.2.2 General spot film........................................................................................... 68

5.2.3 Pensile filer radiography.................................................................................. 70

5.2.4 Operation Instruction of Workstation........................................................... 70

CHAPTER6 MAINTENANCE........................................................................................... 106

6.1 Maintenance the operator can carry out and clean....................................................106

6.2 Maintenance that can be carried out and cleaned by the Authorised Technician..... 108

6.4 Fault Code and Failure Removal.............................................................................. 110

CHAPTER7 ATTACHMENT................................................................................................. 116

7.1 Spare parts list........................................................................................................... 116

7.2 Safety Performance Inspection Report..................................................................... 117

7.3 Packing list................................................................................................................ 118

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CHAPTER1 OVERVIEW

1.1 Use of the equipment

This unit can be used for X-ray routine inspections such as X-ray stomach and intestines

spot film photography, remote control compartment fluoroscopy and other traumatic

photography in medical teaching, scientific research and medical treatment units: It can

conduct digestive tract radiography, biliary tract radiography, urinary tract radiography and

lower limb venae radiography, etc.; it can carry out fluoroscopy inspection and spot film

photography on esophagus, chest, stomach and intestines, abdomen and four limbs; it also

can implement fracture recovery and getting foreign matters under fluoroscopy, etc.

1.2 Main structure and feature of the equipment

This equipment mainly consists of diagnostic table, high-frequency and high-voltage

generator, operating console , X-ray tube assembly, motorize collimator, high-frequency

diagnostic table control cabinet, see Figure 1-1.

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1– X-ray tube assembly 2 – Collimator 3– Detecting device 4– Diagnostic table


5 – Console 6 –DR acquisition, diagnostic workstation 7– High-frequency and high-voltage generator
Figure 1-1

Main features:

1. Radiographic table
● Visual display man-machine interface and touch screen control makes man-machine
dialogue more direct-viewing, convenient and easy to understand.
● Programmable control device technology with high control precision, good stability and
excellent anti-interference performance.
● Frequency converter control technology, the table operates with soft startup and soft
shutdown, which is smooth without noise and the positioning is more accurate.
● Reliable angular displacement sensor technology with excellent precision, little
dynamic noise and long mechanical service life.
● High-resolution rotary encoder with automatic slicing accuracy, which is safe and
stable.
● Rotational range: 90° ~ 0° ~ -25°, it can carry out conventional examinations about
alimentary organs, and it also can be used for a variety of special examinations.
● Humanized design of diagnostic table side switch, which is more convenient for
positioning when operating near the console.
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● Toshiba high-quality image enhancement device, which further improves image clarity
and contrast ratio, and makes it much easier and clearer to identify the nidus.
● The moving range of spot-film device is wide, so we adopt the operating mode with
machine moving but people unmoving, which thus simplifies the implementation of a
series of inspections from the throat and esophagus to the lower abdomen.
● Spot film device load automatically, and the operation process is safe and reliable.
2. Generator
● Generator with X-ray radiography and fluoroscopy functions and its maximum output
power is 80kW.
● Output voltage is 150kV.
● Smaller and lighter block design
● During exposure, you can adjust kV and mA buttons to achieve constant ray output.
● Large screen LCD flat panel display, which is used to display APR conditions and
practical conventional items.
● User-friendly operating system configuration.
● The operator can modify APR technology items.
● APR/ray bulb tube data download function.
● A variety of diagnostic procedures with prompt information for the operator.
● Equipped with serial RS232 communication interface.
● You can carry out operation programming for APR alone or choose programs for APR
and manual technology items.
● Programmable settings, calibration and implementation of APR routine operation (by
connecting it with an external computer).
● It is allowable to select four kV and mA curves for ABS (automatic brightness
stabilization) circuit.

1.3 Standards and specifications

GB/T 191—2008 Packing, storage flag icon

GB 9706.1—2007 Medical electrical equipment Part 1: General requirements for

safety

GB 9706.3—2000 Medical electrical equipment Part II: high voltage generator

requirements for safety devices diagnostic X-rays occur.

GB 9706.11—1997 Medical electrical equipment Part II: Medical diagnostic X-ray

source assemblies and X-ray tube assembly requirements for the


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safety

GB 9706.12—1997 Medical electrical equipment Part I: General requirements for

safety - Collateral standard radiation protection in diagnostic X-ray

equipment General requirements

GB 9706.14—1997 Medical electrical equipment Part II: Safety ancillary equipment

requirements for X-ray equipment

GB 9706.15—2008 Medical electrical equipment Part I: General Requirements for

Safety 1, Collateral standard: Safety requirements for medical

electrical systems

GB 9969.1 Industrial Product Manual General

GB/T 19042.1—2003 Evaluation of medical imaging departments and routine testing -

Part 3-1: X-ray imaging and fluoroscopy imaging systems using

X-ray equipment performance acceptance tests

YY 0076—1992 Coating classifications for metal product Technical conditions

YY 0466—2003 Medical devices -- Symbols to be used with medical device labels,

labeling and information to be supplied

YY/T 0106—2008 General specifications for medical diagnostic X-ray equipment

YY/T 0291—2007 Environmental requirements and test methods for medical x-ray

equipment

YY/T 1099—2007 Medical X-ray equipment -- Designation, packaging,

transportation and storage

Medical equipment specification 、Labels and packaging labeling regulations (The state

food and drug administration 2007.7.8 no.10)

1.4 Quality Assurance

1.4.1 Responsibilities of manufacturer

The manufacturer will be liable for quality of the equipment in aspects of safety, reliability
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and performance under the following conditions:
1. Installation, adjustment, modification and maintenance are conducted by personnel of our
company or personnel authorized by our company;
2. All electric utilities of the equipment comply with requirements of the Manual;
3. Operators of the equipment are well trained and skilled technical personnel and operate
strictly in accordance with the Manual.

1.4.2 Three guarantees

1. Under the precondition that the user complies with above provisions, within one year

after delivery, for any quality problem or failure in normal using of the equipment, the

company will repair or change parts for the user free of charge or even accept return.

2. For equipment damage due to non-compliance of the user to above provisions or

equipment exceeding 1 year after delivery, the company may repair or replace parts for

the users, but maintenance fee will be charged.

3. The company provides ordinary maintenance service for equipment within 8 years of

service life under correct using condition.

1.5 Attentions for Safe Operation

1.5.1 General rules

This Manual is for the purpose of guiding certified radiographer on safe operation. As

radioactive equipment, this equipment will be operated strictly according to provisions of

the Manual and cannot be used for other purpose except medical radiography. This

equipment can only be used by trained personnel with needed radiation knowledge. Special

attention will be paid on the following matters during using:

1. The equipment with any electric or mechanical fault will not be used.
2. It is not allowed to remove protective circuit or protective device to make the
equipment work under power.
3. It does not allow using the equipment under moist, inflammable and explosive
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environment.
4. Consent of our Company or maintenance personnel authorized by the Company shall
be obtained from any modification to the equipment.
5. It shall be ensured that replacing components of the equipment will not endanger any
patient or operator; where necessary, maintenance personnel of our company may be
contacted.

Improper operation may result in damage to the equipment; hence regular inspection and
maintenance are necessary.

The company will be liable for any personal and property losses caused by the equipment,
excluding that due to non-compliance to the Manual or modifying the system without
authorization.

1.5.2 Electric safety

1. Ensure network voltage and current meet requirements of the equipment on power.
2. The equipment shall be put in well-ventilated room without flammable and combustible
gas leakage.
3. Cleaning, disinfection and sterilization shall be conducted when the complete machine
is power off.
4. If the floor where the high voltage generator locates is not made of wood, the generator
shall be put on wood base.
5. Shut off the machine and switch off the power after using.

1.5.3 X-ray safety protection

Every time before exposure, it shall be ensured to adopt measures to prevent X-ray and keep

in mind the following matters:

1. Wear protective clothes and goggles for bedside work;

2. Operate in compartment to the greatest extent to be far away from X-ray source;

3. Low dose exposure to the greatest extent under permitted projection condition.

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1.5.4 The effective occupation

The effective occupation is as shown in Figure 2 and Figure3.

Figure 1-2 Effective occupation of radiographic table in horizontal position

Figure 1-3 Effective occupation of radiographic table in 90°position

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1.5.5 Environmental risks and treatment

When the equipment is retired, the X-ray tube assembly and transformer oil in high voltage

generator shall be reclaimed by specialized industrial waste and waster oil collection station;

while other steel and cooper materials shall be reclaimed by corresponding department.In

particular, the equipment contains the following materials and/or components:

● “Reducers”: lubricating oil, steel, aluminium

● Motor: iron, copper, hard plastic material casings

● Electric cabinet: iron, aluminium, copper, non-biodegradable plastics, vetronite for

printed circuits.

1.5.6 Retirement of equipment

Service life of the equipment under correct using condition is 8 years; wherein, normal

service life of key component X-ray tube is 10,000 times; damaged X-ray tube may be sent

to our company for replacement. If the equipment is damaged after correct using for 8 years

and is beyond repair, such equipment shall be retired.

1.6 Use logo identity

Symbol description:

Radiography Dangerous Ionizing

voltage radiation
Small Focal Type-B Protective

spot symbol equipment grounding


Large focal “Speaking” “Listening”

spot symbol device device


Talkback Emergency
Fluoroscopy
conversion stop

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1.6.1 External label

1. Equipment nameplate (see Figure 4)

Figure 1-6

2. High-voltage generator nameplate (see Figure 5)

Figure 1-5
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3. Console nameplate (see Figure 6)

Figure 1-6

4. Radiographic table Control Cabinet nameplate ( see Figure 7)

Figure 1-7

5. Radiographic table nameplate (see Figure 8)

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Figure 1-8

6. Electric Collimator nameplate (see Figure 9)

Figure 1-9

7. X ray tube assembly nameplate(see Figure10)

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Figure 1-10

1.6.2 Equipment nameplate location

The equipment nameplate location is as shown in Figure11.

Figure 1-11

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1.7 ENVIRONMENTAL SPECIFICATIONS

1.7.1 The room requirements and Layouts

The room requirements of diagnostic table:

1. Machine room area: no less than 5000×4000mm.

2. Control room area: 5000×2500mm; the control room shall be opening on to the

machine

room, and the observation window shall be equipped with lead glass.

3. Machine room height: at least 2800mm.

4. Machine room door: Width: 1500mm; height: 2300mm.

5. The diagnostic table shall be directly fixed on ground base which shall be horizontal

and can bear 1500kg of load.

Attention: The foundation shall adopt cement with grade no less

than 400" and casting thickness no less than 200mm.

6. Cable duct shall be set with cover plate parallel to the ground.

7. The machine room shall be equipped with special ground wire with ground resistance

not exceeding 4Ω.

8. Protection capability of the machine room to X-ray shall meet requirements of related

national regulations.

The layout of machine room is as shown in Figure12.

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Figure 1-12 Layout of machine room

1.7.2 Electrical requirements

1. Power conditions:

● Three-phase four-wire a.c.380V±38V, 50Hz±1Hz;

● Internal resistance of power source shall not exceed 0.13Ω;

● Power capacity shall be no less than 85kVA.

2. The power distribution box shall be equipped with three-phase main switch with rated
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voltage of 500V and rated current of 130A as the switch to break power supply network;

the power distribution box must be firmly fixed on the wall with no less than 1.5m of

height from the indoor floor. Besides, power supply with capacity no less than 85KVA

and independent ground wire (no more than 4 ohm) shall be provided.

1.7.3 Environmental conditions

OPERATING

● Ambient temperature: 10℃ ~ 40℃

● relative humidity: 30% ~ 85%

● atmospheric pressure: 70kPa ~ 106kPa

TRANSPORT AND STORAGE

● Ambient temperature range: -20 to 70 °C.

● Relative humidity: 10 to 95%, including condensation.

● Atmospheric pressure range: 500 to 1060 hPa (375 to 795 mm Hg).

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CHAPTER2 TECHNICAL PARAMETERS

2.1 X-ray high voltage generator

1. Maximum power: 50kW

2. kV range: 40 ~ 150kV

3. mA range: radiography: 10 ~ 630mA

4. mAs range: 0. 1 ~ 630mAs

5. Time range: radiography: 1.0 ~ 6300ms

2.2 X-ray tube assembly

Attention:

● X-ray tube assembly equipped to this equipment (hereinafter referred to as

assembly) only applies to medical Radiographic.

Pay attention to that load exceeding the stipulated condition is not allowed,

because overload operation may result in damage to tube sleeve and X-ray tube.

The assembly is equipped with normally-closed temperature switch, which will

start when wall temperature of the assembly reaches 75°C.

● The assembly will generate X-ray while working under high voltage; therefore

attention shall be paid to protect it during operation and adjustment.

● Using the assembly in the environment with inflammable or poisonous gas is not

allowed.

The operation environment temperature is 10 ℃ ~ 40 ℃ , relative humidity is

30%~85% and the atmospheric pressure is (70~106)kPa.

As for transportation and storage environment conditions, the temperature range

is -20℃~70℃, the relative humidity is 20%~90% and the atmospheric pressure is


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(50~106)kPa.

● Inside the assembly, there’s glass X-ray tube mounted, hence it shall be handled

gently during transportation and installation to avoid damage to X-ray tube.

● As per the national regulations, installation, adjustment and using of the assembly

shall be carry out by personnel with professional qualification certificates.


● 1.Model of X-ray tube assembly: E7252X
● 2.Grade of X-ray tube assembly: Grade Ⅰ Type B
● 3. Manufacturer of X-ray tube assembly: Toshiba Electron Tubes and Devices Co., Ltd.
● 4. Parameters of X-ray tube:
● X-ray tube model: E7252
● Target material: Molybdenum base rhenium – tungsten composite target
● Basic shaft involved in target angle and focal spot of X-ray tube: the straight line perpendicular to shaft axis
of X-ray tube and passing through window mark point.
● Anode target face angle of X-ray tube: 12º
● Nominal focal spot value: Large focal spot: 1.2mm; small focal spot: 0.6mm
● Tolerance of focal spot center of X-ray tube to basic shaft: <1.5mm
● Maximum operation tube voltage: Fluoroscopy: 125kV Max; exposure: 150kV Max
● Maximum anode input power: Large focal spot: 75kW; small focal spot: 27kW
● Maximum anode thermal capacity: 210KJ
● Filament volt-ampere characteristics of X-ray tube:
● Large focal spot (5.5A): AC 12.7 ~ 17.1V
● Small focal spot (5.2A): AC 7.0 ~ 9.4V
● Filament frequency limit of X-ray tube: 0~25 kHz
● Inherent filtration of X-ray tube: 0.9 mmAl/75kV
● Anode rotate speed of X-ray tube: 50Hz: 2700rpm; 150Hz: 8100rpm
● Maximum anode heating power of X-ray tube: 475W (667HU/s)

● 5. Stator parameters
Item Starting Running
Power frequency (Hz) 50 50
Voltage (V) 240 58
Min acceleration time (S) 0.6 —
Phase-splitting electric 24 24
capacity(μF)
● 6. Insulation resistance of stator between outgoing line and tube case: 2MΩ (Min)

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● 7. Total filtration of assembly: ≥1.9 mmAl (75kV)


● 8.Radiation protection of the assembly shall meet GB9706.12 III. General Requirements on
Radiation Protection of X-ray Diagnosis Equipment of Part I: General Safety Requirements
of Medical Electric Device (idt IEC601-1-3), i.e. 150kV 3.4mA.
● 9. Radiation field of assembly: when SID 835mm, 354mm×354mm
● 10.Assembly weight (approximate): 18kg
● 11.High voltage cable interface of the assembly shall comply with IEC 60526.
● 12.Cooling medium: transformer oil with temperature ≤75℃
● 13. Cooling method of assembly: natural cooling
● 14.Thermal capacity of assembly: 900kJ (1250kHU)
● 15. Max. cooling velocity of assembly (natural cooling): 200W(16HU/min)
● 16. Refer to Figure2- 1 for emission characteristics of X-ray tube.

Figure 2-1 Filament emission characteristics of X-ray tube


● 17 .Refer to Figure2- 2 for load characteristics of X-ray tube.

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Figure2-2 Load characteristics curve (three-phase 50Hz)


● 18. Refer to Figure 2-3 for anode thermal characteristics of X-ray tube.

Figure 2-3 Anode thermal characteristics of X-ray tube

● 19. Refer to Figure 2-4 for cooling characteristics of assembly.

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Figure 2-4 Thermal characteristics of X-ray tube assembly

● 20. Refer to Figure 2-5 for anode plate wiring of assembly.

NC: No connection
ET: Grounding terminal
M: Main terminal of stator
A: Auxiliary terminal of stator

Figure 2-5 Anode terminal wiring diagram

● 21. Refer to Figure 2-6 for overall dimensions of assembly.

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Figure 2-6 Outline drawings

2.3 Collimator

1. Radiation field:

● Shape of radiation field: rectangle

● Minimum radiation field: when SID is 100 cm, the limit of the Collimator should be not

more than 5 cm x 5 cm

● Maximum radiation field: 345 ㎜×345 ㎜ (source image distance: 835mm)

2. Illumination of visible light:

Central average illumination: >100Lux

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Lighting ratio: >4

3. Lamp: halogen lamp, 24V, 100W


4. irradiation time: 5-45s, can be set
5. Filtration:

Inherent filtration: 1.5mmAl

6. Lead equivalent of shielding blade: 3mmpb (intermediate blade: 2mmpb)

7. Drive mode of blade:

Remote button operation and Local operating button: motor-driven

8. Overall dimensions: 225mm×262mm×210mm (length × width × height)

9. Weight: about 9.0kg

10. Power: DC24V

2.4 Radiographic table

1. Table rotation: +90° ~ 0° ~ -15°

2. Lateral movement of the table: 250mm

3. Table panel load bearing: 500kg

4. Table panel equivalent filtration: not more than 1.2mmAl


5. Pillar longitudinal movement range: 970mm
6. Distance between the focal spot and the film of X-ray bulb tube: 1000 ~ 1800 mm

adjust it by the electric adjustment

2.5 Flat-panel detector

1、Plate type: FDX4343R

2、Tablet manufacturers: Toshiba

3、Tablet parameters:

Effective area: 430(H)×439(V)

Phase element matrix: 3008(H)×3072(V)

Phase element spacing: 143 μm

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Cycle time: Less than 6S

Limit of resolution: 3.5 lp/mm typ

A / D conversion: 14 bit

Energy range: 40 - 150 kVp

Biggest entrance dose (low gain): 4 mR / frame

Data output: 16-bit digital output Ethernet(1000BASE - T)

Command control: Ethernet(1000BASE - T)

Synchronization control: external

Power input: DC 24V 2A

4、Components and characteristics

Sensor protection board: Carbon fiber sheet

Cooling: Natural air cooling

Input: DC 24V

Power consumption: Biggest 20W

Overall dimensions: 512 x 495 x 43 mm (W(H) x D (V) x H )

Weight: 17 kg

5、Environmental conditions

Temperature: 10℃ ~ 35 ℃

Relative humidity: 30 % ~ 85 %

Atmospheric pressure: 70 kPa ~ 106 kPa

6、Storage conditions

Temperature: -15 ℃ ~ 55 ℃

Relative humidity: 10% ~ 90 %

Atmospheric pressure: 50 kPa ~ 106 kPa

2.6 Loading Factor Combination

focus mA kV S
Small focus 10、12.5、16、20、25、32 150 6.3

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150 5.0
40
145 6.3
150 3.2
50
116 6.3
150 2.5
63
92 6.3
150 1.0
80
72 6.3
150 0.32
100
58 6.3
150 0.125
125
51 5.0
138 0.01
160
48 3.2
110 0.0125
200
42 2.5

88 0.0125
250
50 0.63

10、12.5、16、20、25、32、40、
150 6.3
50、63

150 5.0
80
137 6.3
150 3.2
100
110 6.3
Large focus
150 2.0
125
98 5
150 1.0
160
96 3.2
150 0.5
200
86 2.5

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150 0.25
250
69 2.5
150 0.125
320
64 1.6
125 0.1
400
56 1.25
100 0.1
500
45 1.25
79 0.1
630
60 0.25

2.7 Earth leakage current

Normal condition: ≤5mA,single failure state: ≤10mA.

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CHAPTER3 SYMBOLS DESCRIPTION ON EQUIPMENT

3.1 Symbols description on X-ray Generator operation panel

Figure 3-1 X-ray Generator operation panel

LEGEND:
1. Power ON and OFF buttons
2. PREP and X-RAY EXPOSE buttons, and PREP and X-RAY EXPOSURE indicators
3. Radiography controls and display
4. Image receptor buttons
5. Anatomical programming controls and display, BACK / FORWARD buttons, and
6. MENU (reset) button

3.1.1 Power and exposure control


Power On, Power Off Press ON or to switch the X-Ray generator on.
The console will light up and a brief self -
check will be performed.
All front panel LEDs, including the X-Ray

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exposure LED, should light briefly. This is an
LED self – test and does NOT indicate the
presence of X-RAYS.The speaker should
briefly beep near the end of theconsole
self-test.
Press the MENU (reset) button to continue if
anyerror messages are presented.

Press OFF or to switch the generator


off.

Prep, X-Ray Exposure and


Exposure Indicator
Press and hold the PREP or button to
spin the rotor. The prep indicator LED will light
when ready to make an exposure.

While pressing the prep or button, press

and hold the EXPOSE or button to


make an X-Ray exposure.

The X-Ray exposure indicator will light


when an X-Ray exposure is being taken.

Pressing the EXPOSE or button only will


cycle the generator through prep and then
exposure.
When the prep button is pressed, SPINNING
ROTOR will be displayed in the LCD display
window.
When the prep cycle is complete, X-RAY
READY will be displayed in the LCD display
window.
During the X-Ray exposure, X-RAY ON will be
displayed in the LCD display window.
HAND SWITCH (Optional): Press the hand switch halfway to the PREP position. This
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will spin the rotor. Fully depress and hold the hand switch in the EXPOSE position to
make an X-ray exposure.

3.1.2 X-ray radiography control and display

Figure 3-2 Radiography control and display

LEGEND:
1. Technique select button and indicators.
2. Field select buttons and indicators.
3. Film / Screen select button and indicators.
4. Focus select button and indicators.
5. kV up / down buttons and display (non-CM thickness mode).
CM thickness up / down buttons and display (CM thickness mode).
6. mA up / down buttons and display (non-CM thickness mode).
kV up / down buttons and display (CM thickness mode).
7. Density / ms / mAs up / down buttons and display.
8. ms / mAs readout.
9. AEC - ON indicator / post-mAs display.

Technique Select Button and This function may be disabled in programming.


Indicators Press the MODE button until the appropriate
LED lights to indicate the desired technique.

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AEC orfor Automatic Exposure Control (1 point


technique). mAs for mAs technique (2 point
technique). mA/mS for mA and ms technique (3
point technique).

PLEASE NOTE THE FOLLOWING WHEN IN CM-THICKNESS MODE:


• If you are in CM-thickness (AEC mode), and then select CM-thickness (mAs mode)
via the technique selector button, the previously set backup mAs will be displayed for
that CM thickness. Press the CM - or + buttons to update the display and use the
normal mAs, not the backup mAs that was carried forward.
• If you are in CM-thickness (mAs mode), and then select CM-thickness (AEC mode)
via the technique selector button, the displayed backup ms will be based on the
programmed mAs for that CM thickness. Press the CM - or + buttons to set the
backup
ms display to use the appropriate backup ms, not the value that was carried forward.

3.1.3 Field Select Buttons and Indicators (for AEC only)

Press the appropriate field select button(s) to


select the desired field or combination of fields.
The adjacent LED(s) will light to indicate the
selected field(s). All three fields may not be
deselected.
Operates only when AEC is selected.

Film / Screen Select Button


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and Indicators. In AEC mode, press the FILM SCREEN orbutton


to select the desired film / screen combination.
The appropriate LED will light to indicate the
desired selection.
I for film / screen I.
II for film / screen II.
III for film / screen III.
This adjusts the dose to maintain the correct
optical density.
In non-AEC mode, indicates which film / screen
has been
programmed for the selected APR. The
corresponding film /
Focus Select Button and screen combination should then be used for that
Indicators exposure.

Press the FOCAL SPOT button until the


appropriate LED lights to indicate the desired
focal spot.

SMALL or for small focus.

LARGE or for large focus.

This function may be programmed for auto focal


spot selection.

The rate of scrolling for the kV, mA, and ms display increases if the
buttons are pressed continuously. To return to the slowest scroll rate,
release the button(s) and start again.

kV up / down buttons and display (CM up / down buttons and display in CM-thickness mode)

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To increase kV / CM thickness, press +.
To decrease kV / CM thickness, press -.
Displays demanded kVp of the exposure.
Displays selected CM thickness when
CM-thickness function is active.

mA up / down buttons and display (kV up / down buttons and display in CM-thickness
mode)
To increase mA / kV, press +.
To decrease mA / kV, press -.
Displays demanded mA of the exposure.
This is active for AEC in non CM-thickness
mode or mA/ms techniques only.
Displays kV when the CM-thickness function is
active.

3.1.4 Density / ms / mAs up / down buttons and display

For non CM-thickness mode: To increase density, ms, mAs, or backup


ms/mAs press +.
To decrease density, ms, mAs, or backup
ms/mAs press -.
IN AEC MODE:
Displays DENS (density) when “fixed” AEC
backup mode is selected.
Displays DENS and backup ms when “variable
ms” AEC backup mode is selected. Displays
DENS and backup mAs when “variable mAs”
AEC backup mode is selected.
DENS will be displayed above or below the
backup ms / mAs in these modes, depending on

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setting.
The + / - buttons only adjust the parameter
displayed on top. To swap the density and the
backup ms or mAs displays, press both the -
and + density buttons. Refer toSetting AEC
Backup ms or mAs for further details.
The density range is typically -5 to +5. (Installer
programmable to have a range of up to -8 to +8).
This varies the optical density by changing the
dose.
The % dose change per density step change is
installer programmable.
Displays mAs when mAs is selected.
Displays time (ms) when mA/ms is selected.

To increase density, ms, or mAs press +.


To decrease density, ms, or mAs press -.
Displays DENS (density) when AEC is selected.
The density range is typically -5 to +5. (Installer
For CM thickness mode: programmable to have a range of up to -8 to +8).
This varies the optical density by changing the
dose.
The % dose change per density step change is
installer programmable.
Displays mAs when mAs is selected.
Displays time (ms) when mA/ms is selected.

ms / mAs readout
The significance of the ms/mAs readout varies, depending on mode selected:
• In AEC mode, with fixed backup time selected, the AEC backup time is displayed.
• In AEC mode, with either variable ms or variable mAs backup time, the backup mAs
or ms value is displayed.
• In mAs mode, the calculated exposure ms will be displayed (based on the mAs

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selected).
• In mA/ms mode, the calculated mAs of the exposure will be displayed (based on the
mA and ms selected).
AEC - ON indicator / post-mAs display
Displays AEC when AEC is selected.
Displays Post mAs after an AEC exposure.

3.1.5 Setting AEC backup ms or mAs (applies to non CM-thickness mode


only)
The AEC backup mode is installer programmable for each receptor. If FIXED AEC
backup time has been programmed for the selected receptor, the backup ms and mAs
cannot be adjusted.
If the selected receptor is programmed for FIXED mode, density (DENS) only is
displayed, as in the top figure, below. If ms or mAs AEC backup has been selected,
the AEC backup ms or mAs respectively may be operator adjusted. Follow the steps
below.
1. If variable ms AEC backup has been programmed for the selected receptor, press
the + or- buttons shown below to change the AEC backup time.
2. If variable mAs AEC backup has been programmed for the selected receptor, press
the +or - buttons shown below to change the AEC backup mAs.
3. To select density, press both the - and + density buttons. This will swap the density
and AEC backup adjustments. Pressing both buttons again will swap the displays to
allow further adjustment of AEC backup ms or mAs.

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A. Setting AEC backup mAs (CM-thickness mode only)


The AEC backup mAs in CM-thickness mode is set as described in section 4, under
PROGRAMMING CM THICKNESS.
IMAGE RECEPTOR BUTTONS AND INDICATORS

LEGEND:
1. Table, with Bucky, image receptor select.
2. Table, non Bucky, image receptor select.
3. Wall Bucky image receptor select.
4. Auxiliary 1 image receptor select.
5. Auxiliary 2 image receptor select.

Image Receptors (1-5) are depicted as the console is shipped from


the factory. The receptors may have been reprogrammed during
installation. As a result, the receptors may contain installer -
applied icons that differ from those shown in this manual.

Table, with Bucky, Image Receptor


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Press this button to select the table Bucky


image receptor. The adjacent indicator will light.

Wall Bucky Image receptor

Press this button to select the wall Bucky image


receptor. The adjacent indicator will light.

Aux 1 Image Receptor

This is used for CM thickness programming.


Refer to section 4,
Programming the Console, for details.
This function is not enabled in normal operating
mode at this time.

Aux 2 Image Receptor


This function is not available at this time.

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3.1.6 Anatomical programming controls and display

1.For non CM-thickness mode:


Anatomical section and anatomical view selection buttons.
To select an APR technique:
• From the main APR menu (shown in the above figure), press the button next to the
desired anatomical region. The APR display will show anatomical views within that
region. Pressing button 6B (forward) if >> is displayed will show additional
anatomical views within that region. Pressing button 6A (back) if << is displayed
will
return to the previous anatomical views.
• Press the button for the required anatomical view. The selected view will be
highlighted and the image receptor symbol will be replaced with a normal size
patient symbol.
• Press the function button again to toggle between normal, large and small patient
sizes.
• The LCD display will show the programmed X-Ray technique factors.
You may override the programmed techniques by pressing the appropriate selection
button (the ability to override the AEC / mAs / mA/ms function may be disabled in
programming). When any of the default techniques have been changed, the highlight
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will be replaced with a rectangular outline around the anatomical view. Simply
overriding the programmed parameters will not change the programmed
parameters. To make permanent changes to the APR, see CHAPTER 4:
PROGRAMMING THE CONSOLE.
For CM thickness mode:
Anatomical section and anatomical view selection buttons.

CM thickness mode is only available if it has been enabled in


programming. This must be done by your service representative.
CM thickness with AEC is only available on image receptors that
are programmed for “variable mAs” AEC backup. CM thickness
(mAs) is available with all AEC backup configurations.
CM thickness is only available when an anatomical view is selected.
If an anatomical view has not been selected, the technique selector button selects
mA/ms-mAs-AEC in non CM-thickness mode. When an anatomical view has been
selected, the technique selector button selects mA/ms-mAs-AEC in a combination of
CM thickness and non CM-thickness modes as depicted below.

To select an APR technique:


• From the main APR menu (shown in the figure on the previous page), press the
button next to the desired anatomical region. The APR display will show
anatomical
views within that region. Pressing button 6B (forward) if >> is displayed will show
additional anatomical views within that region. Pressing button 6A (back) if << is

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displayed will return to the previous anatomical views.


Press the button for the required anatomical view. The selected view will be
highlighted and the image receptor symbol will be replaced with a normal size
patient symbol. The patient size cannot be changed in CM thickness mode.
The LCD display will show the programmed X-Ray technique factors.
The mid value of the programmed CM range will initially be displayed. Pressing + or
- will scroll through the available CM range for that anatomical view.
The kV and / or mAs is varied automatically as the CM is changed.
You may override the programmed techniques by pressing the appropriate selection
button (the ability to override the AEC / mAs / mA/ms function may be disabled in
programming). When any of the default techniques have been changed, the highlight
will be replaced with a rectangular outline around the anatomical view. Simply
overriding the programmed parameters will not change the programmed
parameters. To make permanent changes to the APR, see CHAPTER 4:
PROGRAMMING THE CONSOLE.
2. Tube 1 display.
This indicator will display TUBE 1 at all times.
3.Anode heat indicator (%HU) readout.
Indicates the tube anode heat for the selected X-Ray tube. An anode heat-warning
message will be displayed at an installer-programmable level, typically 80 % of the
maximum tube H.U. rating. Exposures that will exceed a value of typically 90 % of the
tube H.U. rating will be inhibited (this is also installer programmable).
4.Time readout - 24 hour mode.
The current time is displayed in 24 hour format.
5.Status and operator message display area.
This area shows status, warning, and error messages.
6. Back (<<) and forward (>>) selection buttons 6A and 6B.
Press button 6A (BACK) and button 6B (FORWARD) to scroll forward or backward
through the display. The symbols << or >> will be displayed when these buttons are
active.
7. MENU button.
• Press the MENU button to return to the main menu when in one of the APR
submenus. RESET will be displayed below the MENU button when this is active.

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• Pressing this button will clear error messages.

THE FACTORY-DEFAULT X-RAY TECHNIQUE FACTORS


MUST BE CONFIRMED AS BEING SUITABLE FOR THE
APPLICATION. THESE SHOULD BE EDITED AS
REQUIRED, WITH THE UPDATED TECHNIQUE FACTORS
SAVED AS PER CHAPTER 4.

3.2 Symbols description on operation panel of remote console

Figure 3-6 The operation panel of remote console

Switch machine button : Control equipment power supply


power on and power off.

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Emergency stop button:Protect control


Press this button to make equipment power outage.

Intercom button : MIC control


triangle up for increase volume, triangle down for lower
the volume.
Generator button : Exposure control
Preparation and exposure buttons

Collimator view lamp button:


Using this button will open the view of Collimator

Collimator Open button longitudinally:


press this button to open vertical lead blade of
collimator.
Collimator Close button longitudinally:
Press this button to close vertical lead blade of
collimator.
collimator open button horizontally:
press this button to open transversal lead blade of
collimator.
Collimator Close button horizontally:
press this button to close transversal lead blade of
collimator.
Compressor forward movement button:
press this button to move the compressor forward to press
the body of patient .
Compressor backward movement button:
press this button to move the compressor backward and
far away from the body of patient
Table tilting up button:
press this button to rotate the table to 90o.

Table tilting down key: negative angle button: press this


button to rotate table body in negative direction.

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3.3 Symbols description on local control operation panel of table

Figure 3-7 Local control operation panel

Same as the operation panel of remote console.

Same as the operation panel of remote console.

Same as the operation panel of remote console.

Spot film device longitudinal movement keys:


Move up the button: This button can control the
SFD move up.

Spot film device longitudinal movement keys:


Move down the button: This button can control
the SFD move down.

Tabletop lateral movement keys: move to left


button, This button controls the tabletop move to
left.

Tabletop lateral movement keys: move to right


button, This button controls the tabletop move to
right.

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CHAPTER4 INSTALLATION OF THE EQUIPMENT

4.1 Overview

The equipment must be installed and adjusted by professional personnel of our Company or

authorized by our Company.

Before opening the packing case, it shall be stored in the rain-proof and dust-free

environment; and boxboard shall be opened reasonably while opening the case. While

handling the parts, attention shall be paid to avoid scratching parts surface; check according

to the packing list after opening the case and installation shall only be conducted after

confirming the machine is defect and omission; any problem shall be informed to the

Company for us to dispose in time.

4.2 Installation of radiographic table

4.2.1 Positioning of the fixed bed base

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Figure 4-1: Base installation schematic diagram

According to the figure 4-1 measurement and installation, put the bed well ,radiographic

table directly fixed on the ground,the ground level and can carry 1500 kg load,to build the

basis of using the cement is not less than 400 "label,the ground of the casting thickness not

less than 200 mm.

4.2.2 Column components installed

1—Column components 2—Hex cylinder head screw M12×30 3—pin 4—Hex cylinder head screw M12

×30 5—Scale identification plate 6—Swing arm components 7—Calibration plate bracket

Figure 4-2: column component installation schematic diagram

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1, Post installation. Let the column component (1) pin and swing arm components (6) of

pin hole on a straight line, after inserting pin positioning, Then use M10 x 25 hex

cylinder head screw(5, number of 2), flat washer and spring washer screw in tight, the

column component installation is complete.

2, Scale identification plate installation. Scale will identify plate (5) and scale identification

plate bracket (7, number 2)through M5×10 hex head screw (4, number of 8) connection,

tighten the screws scale identification plate installation is complete.

4.2.3 Tube - limit the installation of beam combination

1—Column components 2—Hex cylinder head screw M12×30 3—Hex cylinder head screw M10×20 4—

Hex cylinder head screw M6×20 5—Tube connection seat 6—Hex cylinder head screw M4×12 7— Tube

outer garment 8—Collimator plate 9—Tube cover mounting plate B 10—Tube lid 11—Collimator

connecting plate 12—Philips countersunk head screw M6×30

Figure 4-3:Tube - limit beam splitter combination installation diagram

1,Preparation: first loosen the two M10 x 20 hex cylinder head screw (3), remove the fixed

bulb connected seat within the M12 x 30 hexagonal cylindrical screw (2), and Remove the

Tube connection seat (5).

2, The installation of the tube connection seat: Connecting lamp holder (5) and bulb
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components with four M6 x 20 cylinder head screw (4) fixed connection, screw down the

screws, Note the tube connection block chamfering direction with the ball tube installed in

the same direction.

3, The installation of plate and the cover cap: according to figure the order of the limit of

the collimator plate (8), tube cover mounting plate (9) and B ball tube (10), the limit of the

beam splitter connecting plate (11) and a light bulb components have four M6 * 30 philips

countersunk screw (12) fixed connection, tighten the screws.

4, Light bulbs and column component connection: The first three steps have assembly bulb

insert column component mounting holes , with M12 x 30 cylinder head screw (2), two

M10 x 20 hex cylinder head screw (3) fixed connection, screw not preloaded, convenient

and subsequent adjustment

5, The installation of the Collimator: Will be limited within the Collimator on four

hexagonal cylindrical screw M5 x 40 screw out but can't fall off, turn the bulb components

to make the ball tube output window level up, lock bulb turn fastening screws, careful drop

collimator bayonet center line connected to the collimator plate and inserted into the slot,

Locking Collimator 4 x 40 M5 inner hexangular set screw, locking Collimator 4 x 40

M5 Hex cylinder head screw, after confirm the connection is firm, loosen the bulb turn

fastening screw (3), turn the bulb components make the bulb output window down.

6, Bolt pre-tightening : after adjust the bulb and tablet of collimation, tighten the pieces of

2, 3, beam splitter installed complete bulb.

7, the installation of tube outer garment: all the installation is completed, the ball tube cover

(7) T slot insert ball tube mounting plate B notches, with two cross trough pan head screws

fixed a M4 x 12 and ball tube cover, screw down the screws.

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4.2.4 Flat-panel detector, ionization chamber, the installation of filter

wire grid

1—Disc 2—The downside cover 3—Philips countersunk head screwM3×10 4—Philips countersunk

head screwM3×6 5—Philips countersunk head screwM3×6 6—Tablet power installation plate 7

— Tablet power 8—Hex cylinder head screw 9—Probe mounting plate 10—Flat-panel detector

11—Ionization chamber 12—Ionization chamber pressure plate 13—Box front cover components

14—Philips countersunk head screw M4 x 10 15—Line filter tray components 16—Hex cylinder head

screw M4 x 10

Figure 4-4: Flat-panel detector, ionization chamber, filter wire grid installation

diagram

1, Plate, the combination of the ionization chamber: as shown in the above, First the

flat-panel detector detector installed in the (9), The mounting holes with ten M4 x 10 philips

countersunk head screw (14) add flat washer and spring washer is fixed, Put ionization

chamber detector, determine the correct position and direction, with ionization chamber

pressure plate (12) and 8 M4 x 16 hex cylinder head screw (8) fixed flat washer and spring

washer, screw down the screws, flat component.

2, Box front cover components, the gear cover, flat power installation plate disassembly:

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Loosen the four M3x10 philips countersunk head screw (3), a box cover components will be

removed, pay attention to protect box cover component of wire. Then four M3x6 philips

countersunk head screw (5), decomposition gear cover (2), and finally loosen the four M3x6

philips countersunk head screw (4), took the tablet power installation plate (6).

3, The installation of tablet power supply:The tablet PC power supply box on the tablet PC

power installation plate (6), the installation hole, with 4 M3 x 6 cross trough pan head

screws (5) combined with fixed flat washer and spring washer fixed connection, tighten the

screws, flat power components.

4, The installation of flat component: The first step has been completed flat component with

six M4 x 10 cylinder head screw (16) and flat washer and spring washer is fixed on the box

(1), confirmed after its aligned with the center line of the ball tube screw down the screws.

5, The installation of tablet power components: Will complete the assembly step 3 tablets

power components with 4 M3 x 6 philips countersunk head screw (2) fixed on the box (1),

screw down the screws.

6, Cover the downside of Ann: Will be descending cover (2) using 4 cubic meters x 6 cross

trough pan head screws (5) combined with flat washer is fixed on the box (1), screw down

the screws.

7, The installation of box front cover components: The box cover components (13) with 4

M3 x 10 philips countersunk head screw (3) fixed to the boxes (1), screw down the screws.

8, The installation of line filter tray components: Filter tray component (15) from the box

cover component opened-toe inserted into the box about the line filter chute, the assembly is

complete.

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4.2.5 After the decorative shell installation (the machine debugging)

1— Adornment casing 2 2—Adornment casing 3 3—Swing arm components 4—Trough pan head
screw M4 x 10 5—Piece of box cover

Figure 4-5: Adornment casing installation schematic diagram

1, The shell is installed: With six M4 x 10 cross trough pan head screw washer peace will

decoration housing 2 (1) fixed ,with four M4 x 10 cross trough pan head screw washer for

peace will decorate the shell 3 (2) fixed to the column component, screw down the screws。

2, Box cover installation: After the machine debugging installation box cover,remove the

bed surface to the outside , With four M4 x 10 cross trough pan head screw washer for

peace will box cover (5) and pills box fixed components..

4.3 Equipment cable connection

4.3.1 Power cable and the protection of ground wire

1, the generator power cable PLD80.00.01:

A. more than soft wire, materials for BVR10mm2, light blue color and length is 8 m, are

connected by A generator power terminal N to zero wall gate line, as shown in figure 4-6

"N".
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B. more than soft wire, materials for BVR13mm2, color is black, length is 8 m, the

generator power terminal "L1" "L2" "l" to connect to wall brake line, as shown in figure 4-6

"L1" "L2" "l".

Ground: more than soft wire, materials for BVR4mm2, yellow-green color and length is 8

m.Ground by generator protection earthing terminal connected to wall brake independent

protection ground, as shown in figure 4-6 "ground".

Figure 4-6: High voltage generator power cable wiring diagram

2, power cable photography bed PLD80.00.01:4 core cable, materials for RVV1.5 was x 4,

length is 8 m.Photography bed after the power cable from the generator and the terminal

row of TB - 1504 - l terminal connected to photography bed base line of the X1 "L1" "L2"

"l" and "N".As shown in figure 4-7 "1 - ground" 2 to the power cord ""

Ground: more than soft wire, materials for BVR4mm2, yellow-green color and length is 12

m.Protective earthing terminal connected to ground by photography bed base wall brake

independent protection ground, as shown in figure 4-7 "ground".

Figure 4-7 :Photography bed power cable and protection of ground wire connection
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diagram:

3, probe power cable PLD80.00.03:2 core cable, materials for RVV0.5 was x 2, length is 8

m.Probe power cable terminals from the photography bed base and row X2-2 X2-2

connection and power supply box of EPS plate - F001A.As shown in figure 4-15 "1".

4, other protective grounding line: console protection grounding line, the length is 5 m, the

protective earthing terminal connected to the console base wall brake independent

protection ground;Detector protection grounding line, the length is 5 m, bed sets by

photography base protective earthing terminal connected to the site of the protective

earthing of flat-panel detector;Bulb protection grounding line, the length is 12 m, is

composed of high voltage generator connected to the protective earthing terminal of the ball

tank pipe protection ground E.

Protective earthing line to ensure the safety of equipment and staff,

the user must provide independent meet the national standards for

this equipment protection grounding line, pick up Resistance must

be no greater than 4 Ω.

Wall brake wiring, must ensure that the switch is in the open

circuit state, unless the installation wiring has been completed, or

does not

allow closing!

4.3.2 High voltage generator cable connection

1, anode startup cable PLD80.00.07: from the high voltage generator AUX J7 PWB

BOARD interface to connect to bed bulb components of photography, "2" as shown in

figure 4-8.

Function Bulb Connect to

Secondary winding 3(A) J7-6

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Primary winding 2(M) J7-5

Public side 1(C1) J7-4

Shielding E J7-3

Thermal protection switch 1 5 J7-2

Thermal protection switch 2 6 J7-1

2, exposure control cable DRA20.04: from the high voltage generator AUX J2 PWB

BOARD interface connected to synchronous IO_GEN box interface, as shown in figure 4 to

8 "3".

Function Synchronous box IO_GEN Connect to

RLS_2 8 J2-5

RLS_1 7 J2-6

XPB1- 2 J2-7

XPB1+ 1 J2-8

3, synchronous box POWER cable DRA20.02: from the high voltage generator AUX J11

PWB BOARD interface connected to synchronous POWER socket box interface, as shown

in figure 4 to 8 "4".

Function Synchronous box POWER Connect to

+24V 1,2 J11-2

GND 14,15 J2-6

4, generator CONTROL cable PLD80.00.05: from the high voltage generator CONTROL

BOARD interface J19 to connect to the console interface XZ1 CONTROL box, as shown in

figure 4 to 8 "5".

Function Control box XZ1 Connect to

+12V XZ1-1,2 J19-1,2

READY XZ1-3 J19-3

X-RAY XZ1-4 J19-4

GND XZ1-5 J19-5

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LS1 XZ1-7 J19-7

LS2 XZ1-8 J19-8

ON XZ1-9 J19-9

OFF XZ1-10 J19-10

PREP XZ1-11 J19-11

EXP XZ1-12 J19-12

COM1 XZ1-13 J19-13

COM2 XZ1-14 J19-14

5, generator serial communication cable PLD80.00.06: from the high voltage generator

CONTROL BOARD interface J3 connected to the computer serial port 1, as shown in

figure 4 to 8 "6".

Function Computer serial port 1 Connect to

RXD 3 J22-2

TXD 2 J22-3

GND 5 J22-5

Figure 4-8 :Generator unit cable connection diagram

6, high voltage cable: connect to photography from the high voltage generator fuel tank bed

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bulb components, as shown in figure 4-9 and 1 – anode 2 - the cathode. Two cables

non-polarity restrictions, but before the installation must be prepared to tag, prevent the

anode and the cathode cable meet the cross. Check whether the plugs and high pressure

outlet is clean, or with anhydrous alcohol or ethyl ether scrub clean. Evenly at the top of the

high voltage plug insulation silicon grease, alignment hole reciprocating slowly inserted,

rule out the air of the socket. Finally, tighten gland and locked tightly screw fixation.

Figure 4-9 :High voltage cable connection diagram

High voltage cable bending is not less than 10 times its diameter, as

far as possible to avoid bending. Excessive bending may cause high

voltage cable breakdown, endanger the equipment and personnel

safety.

8, ionization chamber cable PLD80.00.08: from the high voltage generator AEC BOARD

J11 connecting to the ionization chamber extension cable plug amplifier, as shown in figure

4 to 10.

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Function Pre amplifier plug AEC Interface board J11

There is no connection 1 1

Field II(Right field) 2 2

Field I(Among the wild) 3 3

Reset/exposure 4 4

Output signal integral slope 5 5

Field III( Left field) 6 6

-12VDC 7 7

+12VDC 8 8

GND (Shielding) 9 9

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Figure 4-10 :Ionization chamber cable connection diagram

4.3.3 Photography bed cable connection

1 ball tube pillar, photography bed and lathe bed cable connection

1) the bulb out of limit switch cable: swing arm unit left terminal row 9-1, 9-2 and 9-3.

2) the ball tube retracted limit switch cable: swing arm unit left terminal row 10-1, 10-3-2

and 10.

3) ball tube telescopic motor cable: swing arm unit right terminal line of 419 and 420.

As shown in figure 4 - 11.

Figure 4-11 :Tube column cable terminal

2 bed, photography and control box of cable connection

1) the console communication power supply cable PLD80.00.04: from the console

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operation box DB9 serial port/F connecting to photography TABLE bed PCB terminal

terminal row X6 J32 and photography bed base, as shown in figure 4-11 "1".

Function Control box XZ2 Connect to

+12V XZ2-1 X6-9

GND XZ2-2 X6-10

FG XZ2-4 Protect the earth

A XZ2-6 J32-5

B XZ2-7 J32-7

STOP1 XZ2-8 X6-8

STOP2 XZ2-9 X6-7

2) audio power cable PLD80.00.11 from control box air outlet XZ3 connected to terminal

row X5 photography bed base, as shown in figure 4-12 "2";Speaker cable PLD80.00.12

from control box air outlet XZ3 connected to the speaker, as shown in figure 4-12 "3".

Function Control box XZ3 Connect to

SP1 XZ3-1 Horn + Side

SP2 XZ3-2 Horn + Side

0V XZ3-3 X5-11

18V XZ3-5 X5-12

Figure 4-12 :Photography bed and control box cable connection diagram

3, photography bed and limit beam splitter cable connection

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1) vision light cable PLD80.00.10: from terminal diagnosis bed row X5 connection to the

limit of 2 needle beam splitter XZ2 air outlet (2 needle aviation plug), as shown in figure

4-13 "1".

2) limit beam splitter PLD80.00.09: communication power supply cable from photography

TABLE bed PCB terminal J31, power supply and driver PCB terminal J4, diagnosis bed

terminal row X5 of prefabricated cable connector (17 stitches aviation plug) connected to

the limit of beam splitter 17 stitches XZ1 air outlet, as shown in figure 4-13 "2".

1— Power communication cable socket 2—Vision light cable socket

Figure 4-13 : Photography bed and the limit of beam splitter cable connection diagram

4.3.4 Image system cable connection

1, gigabit Ethernet cable DRA20.01: from flat-panel detector Ethernet connection to a

computer network card, as shown in figure 4-14 "1".

2, flat-panel detector control cable DRA20.05: from flat panel detector EXT_1NF interface

to connect to sync box DET_TABLE interface, as shown in figure 4-14 "2".

3, a serial port communication cable DRA20.03: from synchronous box serial COM_PC

connected to the computer serial port 2, as shown in figure 4-14 "3".

4, tablet power cable: from the tablet power supply box connected to the flat panel detector,

"2" as shown in figure 4 to 15.

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Figure 4-14 :Image system cable connection

Figure 4-15 :Tablet power connection diagram

4.4 Final validation

Photography base installation fixed bed, the ball tube - the limit of beam splitter of the

installation, detector and AEC ionization chamber install accurate, confirms the accuracy of

equipment cable connection, fastening good protective earthing line.

Check equipment ac power supply circuit and the dc power supply circuit for short circuit,

especially the power line can't bare or touch metal case.External power supply voltage is

measured with a multimeter, confirm to meet the requirements of the equipment.

Close the wall brake, boot, check equipment without exception.

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CHAPTER5 OPERATION OF THE EQUIPMENT

5.1 Photography debugging of the bed

On the workstation at the same time press the SID of 1.0 m and 1.8 m button, and then press

the power button, can enter the debug state.

According to 1.0 m and 1.8 m button switch can according to positive and negative

direction indicator state changes (1:light),operate the movement control key,measure the

mast swing Angle or bed body up the pour point of view , to adjust to each state in the

column automatically return button to save the current state of the AD value, successfully

saved nearly control plate column automatically return the light 500 ms.

Table 5-1 each AD and LED status indicates the corresponding table

Work station debugging status leds status indicator

LED7(Columns
LED1(1.0m) LED2(1.8m) Instructions
automatically return)

0 0 0 Mast back to 0 (middle) State of the AD

Mast swing + 45 degrees State of the


0 0 1
AD

0 1 0 Mast swing- 45 degrees State of the AD

bed body inverted 90 degrees State of


0 1 1
the AD

bed body inverted 0 degrees State of the


1 0 0
AD

Bed body up down the negative


1 0 1
protection State of the AD

Since the bed body down a negative


1 1 0
Angle State of the AD

1 1 1 The mast swing - 30 degrees State of


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the AD

Potentiometer voltage maximize the mast swing + 45 degrees, the

potentiometer voltage on the bed body 90 degrees is the biggest,

debugging is measured with a multimeter, confirm the accuracy

of

direction, or equipment may be damaged!

Debug state, the Collimator control are described in the following table 5-2 functions.

Collimator keys function state of debugging

Code name Name Functional specifications

Collimator longitudinal Debug mode, manual control ball


KEY_XSQ_Z_O
open button tube rise

Vertical collimator Debug mode, manual control tube


KEY_XSQ_Z_C
close button ball drop

Collimator horizontal Debug mode, automatically set the


KEY_XSQ_H_O
open button light bulb SID

Collimator transverse
KEY_XSQ_H_C Debug mode, manually bulb SID
close button

5.1.1 Photography bed up debugging

A, photography bed up down direction debugging:

Point moving bed body up down buttons (guarantee the bed body is not limit location), the

same direction is marked down direction and key of the bed body the direction is right, if on

the contrary, to exchange the bed body up any two input line of the motor, can make the

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motor reverse.

Pay attention to the potentiometer AD value is in the state

allows motor movements; Only the SID in the lowest limit to

allow the bed body fall sport!

B, photography bed down limit and tuning parameters

Bed body eventually using photoelectric protection restrictions on both ends of the coupling

switch as, potentiometer on testing, on the basis of the restrictions on the rotating

mechanism of installation, as shown in figure:

1/ 2-- Body down restrictions on both ends of the bed 3—Pour the potentiometer

Figure 5-1 : Down limit installation

Must complete debugging by two people, one of the employees to

observe whether there is abnormal situation happen! Lathe bed of

business beyond authorization, not under the bed ban someone or

foreign body, otherwise will result in equipment damage and

casualties.

Debugging:

Confirm lathe bed in level state, the demolition of the limit of protection pour photoelectric
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coupling switch mechanism, loosen the screws of the potentiometer far away from the big

gear, trimmer potentiometer and measure the potentiometer output voltage of 1.2 V at the

same time, fixed screw lock potentiometer, save the bed body in accordance with table 5-1

0 ° bit AD value;

B, slowly raised beds to 89 ° (potentiometer output voltage of 4.70 V or so), save in

accordance with table 5-1 bed body 90 AD value;

C, slow dumping of lathe bed, check whether confirm lathe bed level automatically stop; Or

a potentiometer to adjust the bed down, save 0 ° and 90 ° AD value, and the standard of the

lathe bed between dumping and the vertical position can be automatically stop.

D, lathe bed fall protection AD negative Angle value associated with the protection of

column vertically down, due to bed up negative Angle protection AD value and lathe bed

backward down the negative Angle AD values, are saved in the following method: column

vertical downward movement to limit down protection, dumping of lathe bed, slow

measurement bed down potentiometer output to 1 v, in accordance with the table 5-1 save

bed fall protection a negative Angle AD value; Column vertical upward movement to limit

from down protection, dumping of lathe bed to slow - 14 °, measurement bed down

potentiometer output is about 0.3 V, in accordance with the table 5-1 save bed down a

negative Angle AD value.

E, after the commissioning requirements, installation fixed protection limit photoelectric

coupling switch block slice, observe 90 ° limit and 15 ° protect limit state of the indicator

lights on the corresponding PCB, covering photoelectric coupling limit switch, the lights

went out after normal adjustment 90 ° protection limit photoelectric switch position

coupling and lathe bed up automatically stop and block slice after a difference of 1 mm do

not limit, adjust to 15 ° protection limit photoelectric switch position coupling and lathe bed

has fallen to negative Angle after automatic stop and catch a difference of 1 mm is not limit.

5.1.2 Ball tube pillar longitudinal motion debugging

A, the ball tube pillar longitudinal motion direction debugging:

Inching pillar longitudinal motion buttons (ensure that column is not limit location),
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direction of motion with the same direction is marked key pillar longitudinal motion

direction is correct, if on the contrary, to exchange any two of the pillar longitudinal motion

motor input line, can make the motor reverse.

B, ball tube pillar longitudinal motion limit debugging:

Ball tube pillar longitudinal motion using photoelectric coupling switch as the limit of the

device, installed on the bed body girders, as shown in figure 5-2:

1—Post up limit 2—Pillar down limit protection 3—Pillar down limit

Figure 5-2 : Ball tube pillar longitudinal motion limit

A, make moves down, the post in limit barrier pillar down limit switch photoelectric

coupling column should be able to automatically stop the movement.

B, post up mobile, in limit barrier pillar up limit switch photoelectric coupling column

should be able to automatically stop the movement.

C, adjust the post up limit and pillar down limit, make the pillar of the moving distance of

970 mm.

D, check in bed fall under protection of a negative Angle, column vertical down only to

move down the post protection limit movement.

5.1.3 Debug the bed surface of lateral movement

A lateral movement direction, bed surface debugging:

Point moving bed lateral movement keys (guarantee the bed surface is not limit state),

moving direction and buttons the same direction is marked on the surface of the bed

movement direction is correct, if on the contrary, to exchange bed lateral motion input
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electric draw stem drive line, can make the reverse movement.

1—Bed surface left limit 2—Bed right limit

Figure 5-3 :The bed surface of lateral movement limit

A, make the bed for mobile, in limit barrier bed face left when the limit switch photoelectric

coupling bed should be able to automatically stop motion.

B, make the bed for mobile, right at the limit piece of shade the bed surface limit switch

photoelectric coupling bed surface should be able to automatically stop the movement.

C, adjust the bed left limit moves to the right of the bed and the limit, make the bed surface

mobile travel up to 250 mm.

5.1.4 Ball tube mast swing debugging

A, the tube mast swing direction debugging:

Mast swing inching button (guarantee not limit state) mast swing, swing direction with the

same direction is marked key pillar swing direction is correct, if on the contrary, to

exchange any two input of the mast swing motor drive line, can make the motor reverse.

Pay attention to the potentiometer AD value is in the state allows motor movements.

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1-- Mast swing left limit 2-- Mast swing right limit 3-- Mast swing potentiometer

Figure 5-4 The mast swing the ball tube spacing

A. to bed dumped on the horizontal pillar longitudinal motion to the middle position,

confirm the ball tube column in a vertical state, adjust the mast swing limit switch

photoelectric coupling position outside the range of swing, loosen the potentiometer mast

swing set screw make them away from the big gear and fine-tuning potentiometer and

measure the potentiometer output voltage of 2.50 V at the same time, fixed screw lock

potentiometer, save in accordance with table 5-1 0 ° mast swing an AD value.

B. swing to the left column to + 45 °, measuring pillar potentiometer output is about 4.5 V,

the mast swing save in accordance with table 5-1 + 45 ° AD value; To the right column to -

30 °, save in accordance with table 5-1-30 ° a mast swing AD value; Continue to the right

column to - 45 °, measuring pillar potentiometer output is about 0.5 V, the mast swing save

in accordance with table 5-1-45 ° AD value.

C. swinging the ball tube pillar, check in the plus or minus 0 ° and 45 ° position can be

automatically stop, or to perform a and b.To observe the mast swing control limit switch

corresponding to the indicator lights on the PCB board, cover the photoelectric coupling

limit switch, the lights went out after normal adjust the mast swing left limit switch position

the ball tube mast swing to + 45 ° automatically stopped and does not limit block slice a

difference of 1 mm; Adjust the mast swing position limit switch tube mast swing the ball to

the right - 45 ° after automatic stop and catch a difference of 1 mm is not limit.

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5.1.5 The tube in a sport debugging

1—Tube withdrawal limit 2--Tube into the limit

Figure 5-5 : The tube in a limit diagram

A, the tube in A direction debugging:

In debug state, inching limit beam splitter longitudinal open button (ball tube elevator is not

in the limit state), the tube back (SID) movement is correct, if on the contrary, the exchange

between the electric putter bulb input power cord.

B, ball tube in a movement limit debugging:

Enter debug state press "limit beam transverse off" the ball tube in a set to manual operation,

detection limit, photoelectric coupling switch corresponding to the indicator lights on the

PCB is normal (cover limit turned out).

A, make the bulb into smaller (SID), in the limit block slice keep out ball tube into limit

switch photoelectric coupling tube should be able to automatically stop motion;Make the

bulb back movement (SID), in the limit block slice keep out ball tube withdrawal limit

photoelectric coupling when the switch pipe should be able to automatically stop motion.

B, adjust the pipe into the limit and the ball ball back limit light coupling switch, make the

SID range from 1 m to 1.8 m.

C, debugging is completed, can be set up according to demand the ball tube in a movement

for manual or automatic control.

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Adjustment limit light coupling switch position, must ensure

that the electric draw stem movement is not beyond its limit

position,

or electric putter would be damaged!

5.2 Use of the equipment—General radioscopy/spot film mode

5.2.1 General radiography

When the film holder car is in the ”PARK” position, push the radioscopy footswitch under

console, the system will display images in the real-time. When loosen the footswitch, it will

keep the last image and display automatically.

5.2.2 General spot film

Load the film magazine, the allowable spot film division forms of this kind of film

magazine will be shown on the corresponding position of the interface; if you do not want

to spot film on this film magazine, then you can click "In/Out film" button to take out the

film magazine; it you want to spot film on this film magazine, then click the spot film

division form, then the interface enters the corresponding spot film division form of this

kind of film magazine, after that, you can click "re-selection" to return to the former

interface and select the division form again.

If you select the full spot film mode, then you can implement fluoroscopy or directly press

down the shooting button to implement exposure; after the exposure, click "In/Out film"

button to take out the film magazine.

If you select 2PCS or larger spot film mode, then there would be two kinds of spot film

functions for you to choose from: 1."spot film by area"; 2."automatic spot film".

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1. "Spot film by area": this function allows you to choose any shading area i.e. to implement

exposure only to the selected area; this method requires the operator to remember on

which shading area that he has implemented exposure; otherwise he would implement

exposure on the same area repeatedly. The operating method is as follows:

Click "spot film by area" to enter the interface of spot film by area, it prompts " click to

choose the exposure area directly", click area "1" or area "2", or even area "3" or "4"

among the shading icons, and the selected area is corresponding to the actual film

magazine, after that, you can implement fluoroscopy or press down the shooting button

to implement exposure; click "Back" button, then you can exit from the function of spot

film by area, or you can click "In/Out film" button to take out the film magazine directly;

after selecting the exposure area, click "Cancel", then you can exit from this area; after

exposure, you can return to select another area or take out the cartridge according to

prompts.

2."Automatic spot film": this function is to implement spot film according to area sequence

i.e. according to the area sequence marked with icons, i.e. you can implement exposure

on the next area only when it has been done on the former area, by parity of reasoning,

until it has implemented exposure on all areas, and the operator does not have to worry

about repeated exposure of the same area. The operating method is as follows:

Click "automatic spot film" to enter the interface of automatic spot film, it prompts

"exposure area 1 has been set", and you can implement fluoroscopy or press down the

shooting button to implement exposure directly; click "re-selection" to exit from

automatic spot film mode, and exposure has been done, then it goes to the next area, and

prompts "exposure area X has been done" and "exposure area X has been set", until it has

implement exposure on all areas.

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Fast shooting function: each of the spot film modes has fast shooting function; if you need

fast shooting function, then click "preset cartridges" button, the interface enters fast

shooting page, the trolley moves to the corresponding spot film position, and the collimator

automatically traces to the right position, and now you can press down the shooting button

to implement exposure; fluoroscopy is not allowed during fast shooting; when you want to

cancel fast shooting function, click "Back", then it would return to the previous state

interface;

This operation interface consists of characters combined with icons, thus it makes the

operational procedures more vivid and simpler for operators.

5.2.3 Pensile filer radiography

Radiographic table is in a supine position when it is in photography, the body lie on the

table, put into the cassette, light Collimator field lamp, move the table surface and

longitudinal movement tube column left/right, select the part which need to be photography,

and then select the photography condition. Press the exposure handbrake I file, the tube

anode is start-up, the filament temperature gets high, and the film car moves to the exposure

position. Until the light of “ READY ” is on, press the exposure handbrake II, generator

implement exposure, exposure indicator light is on and "beep" sound is sent out. End of

photography, loosen the hand brake.

5.2.4 Operation Instruction of Workstation

5.2.4.1 Starting Up and Logging in to the System

Steps below only for reference. Steps may be changed


according to your system configuration.

To start up the system and prepare for acquiring patient images,


Steps:
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1、Before power up the host system, please powers up the X-ray generator ,
detector and all the other x-ray system components needed.
2、Make sure that the peripheral X-ray system components are on and working
properly.
3、 Power up the Host PC and login the PC’s operating system
4、Log in to the DROC application.

The DROC HOST PC should be powered down once a day


to ensure a complete system reset. IF NOT , system
performance deteriorates.

The Detector should be powered up at least half an hour


before intended use. If it is used sooner than half an
hour after being powered up, image quality may be
affected.

The following subsections provide specific instructions for each of those steps:
Step 1: Powering up the X-ray generator, detector , etc
Please refer to the related instructions from corresponding manufacturers.
Step2: Checking the System
Once the X-ray generator is powered on, perform the following checks:
● Remove any patient supports or other objects so that they do not interfere
with the movement of the X-ray tube's suspension arm.
● Switch on the collimator’s light to ensure that the area to be exposed to the
X-ray beam is illuminated.
● Check the releases, if applicable, on the X-ray tube's suspension arm, the
Bucky , and the table to ensure that the controls are operating properly.
You can now power up DROC.
Step3: Powering Up the Host PC
Power up the HOST PC and Log in to the PC's operating system;; if the monitor is
not on, press the power button on the monitor.

Before you power on the DROC HOST PC, make sure


the detector have completed their startup sequence
(wait at least several minutes after you power on the
UPS).

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Step 4: Login the DROC application


Start up the DROC application by double clicking the DROC shortcut on desktop.
The login window shows as below:

Figure 23:Log in window

The default password of login is the same to its name. Consult


your System Administrator if you do not know your log-in
password. Passwords are case sensitive, please ensure you
have entered the correct password, if you enter false
password continually for three times, the application will be forced to
exit.

To sign into the application, choose your level from Level Icon (Technician,

Application, Manager) and your name from the User Name drop-down list,

enter your password, and click button .

In case you CAN NOT see this window , and a message box
No Dongle available or Dongle is invalid! DROC System will
exit!” shows up instead. Check your USB license key to make
sure it is well installed or contact our engineers for further
support.

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The initialization window will show the initialization status of the DROC, shown as
below:

Figure 24:Initialization window

There are some initialization tasks of DROC system; the result of each task
(successful or failed) will be displayed one after another.

5.2.4.2 Manage User Account

From System menu (located in the Menu Bar), click User Management menu to
open the User Management window, shown below. When you login with the
manager privilege account, all users are listed. Otherwise, only your own account is
listed.

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Figure 25: User Management window

In this window, you can create a new account, edit the existing user or delete an
existinguser.

You cannot delete your own account.

To create a new account


1. Click New button located in the bottom of the window. The New User window
is showed as below;

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Figure 26: New user window

2. Input the new user’s information and choose a user level you want to create
3. Click OK button to accept the new account, and the New User window closes.
Then the new account information displays in the User list on the User
Management window.
Click Clear button to empty all of new user information, and reenter the information
in New User window.
Click Cancel button to discard the entry of the new user.
To delete an existing user
In the User Management window, choose the user you want to delete and click
Delete button.
To edit user information
1. Choose the specific user you want to edit.
2. Click Edit button located at the bottom of User Management window. The Edit
User window is showed as below.

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Figure 27: Edit User window


3. Edit field(s) according to the description before each field.
Passwords are case sensitive. That asterisk (*) characters
displays for each entered character to protect the privacy of
the password. That requires verifying that you are typing
the new password correctly, since you cannot see what
characters you are typing.

4. Click OK button to save the change.


Click Reset button to empty the fields and then reentered information.
Click Cancel button to discard the editing user information operation.

5.2.4.3 Overview for Capturing Images

The general workflow to acquire and send images to output devices involves the
following steps.
Steps:
1、Identifying the patient and Study;
2、Taking an exposure;
3、 Viewing and accepting the image; Optionally, you can reject the image and
re-capture till an acceptable image is acquired;
4、After all images captured, the data will be transmitted to the default node.
Alternatively, users can send the images to other node or print the images;
5、Closing the patient/Study;
The following subsections provide specific instructions for each of those steps.
Step 1: Identifying the Patient and Study

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Before capturing images, you must identify the patient with whom they are to be
associated. Proper identification ensures that the image data is associated with the
correct patient information.
Depending on the system configuration at your site, there are three ways to identify
the patient from whom you want to acquire images, as described below.

Figure28: Local window


All systems allow you to add/identify patients manually. Whether you are to
acquire images of a new patient or an existing one, you can add/identify manually
by:

● Creating a new patient record in the local database.


● Selecting a patient from those previously created and stored in the worklist
database.
For more information about how to manually specify the patient, refer to the
following topic “Creating a New Patient Locally”.
If your system supports HIS Worklist queries, you can retrieve patient
information from a Radiology Information System (RIS). Refer to the following
topic “Query and Refresh” for more information.
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If your system supports bar code scanning, you can use the bar code scanner to
read the patient ID or some other unique identifying number. If the ID is found in
worklist (if this feature is available) or in the local DROC patient database, the
corresponding patient’s study will be opened. If the ID is not found, you must enter
that patient manually.
The patient/study list in the Worklist window is shown as below:

Figure29: Worklist status bar

There are three status of the patient/study:

SCHEDULED: A new patient/study with no image captured;


IN PROGRESS: An existing patient/study has image/images being captured;
COMPLETED: An existing patient/study with all the images captured.

You can capture images for the patient/study of SCHEDULED or IN PROGRESS status;
even can super-add images to a COMPLETED status patient/study as long as it still
existing in the Local database.

As soon as the patient has been accomplished, it will be stored


as PPACS data. Meanwhile, the completed studies will still being
stored in Worklist table for a certain period after exposure, it
depends on the Space Reclamation Strategy and individual
configuration. Users can pick up the patient still in the Worklist
table and proceed on capturing images. A Study existing in the
PPACS database could not being superadded images any more.
Creating a New Patient Locally

NOTE: Make sure you enter patient names and IDs correctly.
Incorrect entries can cause duplicate patient records for the
same patient. As a result it will be more difficult to find the
patient in future search operations.

To add a new patient without a barcode, fill the information in New Patient page
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on Worklist window.

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The New Patient page is displayed below. Please note that, for your site, the fields in this
window may be different.

Figure30:New Patient Page

In this page, specify the patient information and determine the examination that
patient is going to take.
Fields labeled with an asterisk (*) are required to be filled in. You can switch to the
next field by pressing Tab key. After birthday entered, age is calculated and showed
by system automatically. The name will be displayed in the format
LAST^MIDDLE^FIRST. If you don’t want “^“ character to appear in name, you can
input all content of name in Last Name field.

To save patient information,

● Click Exam button. The patient information will be loaded on the Exam
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window for technicians to capture images.
● Click Save To Local button. The patient information save to local worklist
database and system is still in Worklist window.

When specifying the protocol, click Add Protocol button , the Add Protocol
window shows like below

Figure 31:d Protocol window

UI at your site might be different from thos e described


above.

● Select a Body Part from the left list, the corresponding protocol will be listed in the
upper right area. If select “Often Used” item in the left list, only protocols marked
“often used” display in the upper right area (The often used protocol is defined by
DROC configuration).
● Click the protocol to load the corresponding views into the lower right area.

To delete the view from the lower right area, click Delete Selected View

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button , or click Clear Protocol button to delete all selected view.

To finish the protocol selection, click Ok button.


To cancel the protocol selection, click Cancel button.

1、Emergency Patient Registration (Optional)


To add a patient for emergency, register the patient rapidly and skip all the filling
tasks, click the Emergency button in New Patient page. The system will register a
patient automatically with the name composed of prefix, current date and sequence
number. The sequence number increases 1 by each patient. The prefix of the name,
default procedure and other factors can be modified in Setting window(Refer to
Section E:Emergency Setting Part).Then DROC loads the Exam window directly for
technicians to capture images of this emergency patient.

Figure 32: Exam window for the emergency patient

2、Editing Patient Fundamental Information right after registration (Optional)

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You can edit an emergency patient or locally registered patient fundamental


information before exposure (in fact any time you need as long as it is still in your local
database).

Only the Manager can edit the information. (More details about user account, please
refer to relevant topic of Section E)
1)From the Local page in the Worklist window, select the patient/Study whose
fundamental information you want to correct.

Figure 33: Patient selecting

2)Click Edit button, patient fundamental information editing page


displays with the original information:

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Figure34: Patient Edit Dialog

3)Input the corrected patient information;

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Figure 35: Fundamental information correction

4)Click Accept button to save the correction, the information will be renewed and
shown in the Local page as

Figure 36: After fundamental information correction

As to a newly completed Study, the images will be transmitted


to a default PACS node. Once you have modified an item of
captured image, the new information (for example, a new
name) will be written into the DICOM info. If this patient also
exists in the History list, you can find the related item shows
the new information, too. This Editing operation is only
effective for local database data. It DOES NOT make any
change of the images already transmitted to the PACS node.
We extremely recommend you to resend the Study, which you
just edited, to your desired destination.

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3、Query and Refresh (Optional)

To search an exact patient

From the Query Panel in the Local/Worklist page, you can query a patient/Study by
various searching criteria such as Patient ID, Patient Name, Accession Number
and date.

The Query panel is shown as below:

Figure 37: Query panel

Input the key information associated to the desired patient/Study, and then click
Query button. DROC application will search the local database, and then the result
will be displayed in the Local/Worklist page.

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Figure 38: Searching result list

If multiple patients/studies match the criteria, they will be listed in the Local/Worklist
page.You can locate the exact Study or patient to perform the next operation.
To manually refresh the Worklist from Radiology Information System (RIS)
If your site is connecting to RIS, DROC can retrieve the worklist in background and
automatically refresh the Worklist page. You can override this operation manually
by clicking the Query button.

4、To Delete an item from the Local/Worklist page (Optional)

Only the Manager can delete the item.

Select the patient/Study that you want to delete from the Local/Worklist page; then

click Delete button. A dialogue box will show up.


To confirm deletion, click OK button.

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Figure 39: Delete Confirm Dialogue

Only the local cached worklist item can be removed by this


deleting operation. If retrieved from RIS, it may appear
again.

Step 2: Capturing Images

In this section X-ray exposure dose may be dangerous to the


patient or operator unless safe exposure factors and
operating instructions are observed.

Loading the desired patient/Study to Exam window

To load SINGLE Study:


● Double-click the item in the Local/Worklist page
● The Study is loaded in the Exam Window.

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Figure 40: Study loaded
To load MULTIPLE studies:
From the Local/Worklist page, select several Studies belongs to same patient by
pressing Ctrl + left click mouse; Click the Exam button in Next Step area; Studie
relating to the desired patient are loaded in the Exam Window:

Figure 41: Exam window with two studies

The UI in your site may not show the some buttons after its
installation due to the customization. Please refer to your
support engineer for more details.

You can select a view by highlighting the view icon, and the Study Description will
change as well when you shift between views.

Adjusting Exposure Settings and capturing Sequence (Optional)

At the time the system is installed, default exposure settings and capturing
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sequences are configured according to every specific view. You can use manual
mode or photo timingmode to adjust the default exposure settings.

Figure 42: Exposure Control panel

Technically , you could simply use the default parameters. They should only be
changed for special circumstances, such as a very small person or pulmonary
emphysema.

If you need to adjust the exposure parameters or capturing sequence, refer to Section
C Adjusting exposure parameters for detailed instructions.
Adjusting kV
The range of kV is confined by the generator.
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Figure 43: kV setting


To adjust the kV value, click on the Increase KV button and Decrease KV button
located to the right of the kV value field. The kV value increases and decreases in
steps of 1 kV. Pressing and holding the button causes displayed kV value to increase
or decrease automatically until the button is released. If the kV value reaches
maximum or minimum, the value will remain unchanged.

Changing AEC Settings

The Automatic Exposure Control (AEC) system monitors X-radiation dosage which
is passing through ion chambers and automatically terminates the exposure after
theX-radiation dosage reaches a predetermined amount of radiation.

The default density (0) is calibrated for normal contrast and


density levels. Larger, heavily muscled patients will require an
increase in density. Smaller, lightly muscled patients will
require a decrease in density. However, only use this density
adjustment if the image is grainy. If an image is too dark or
light, adjust the ESA settings (refer to the followed topic
"Changing the ESA Settings of an Acquired Image"); do not
adjust AEC. Typically you use the AEC and detector field
default settings. You can override them under special
circumstances (for example, the patient has only one lung).

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Figure 44: AEC Settings

When using the AEC function, the patient must be


positioned over the enabled AEC field and the radiation
field must be larger than the AEC field. In cases the
preferred radiation field is smaller than the AEC field,
manual techniques are recommended.

You can select AEC detector fields in each ion chamber individually or in any
combination.You can vary the density setting between +4 and -4 (0 is neutral).
To change the density setting, click on the Increase Density button or Decrease
Densitybutton located to the right of Density value field, as shown above. For the
increases or decreases amplitude of each time, please refer to the Service Manual of
Generator.
Adjusting Exposure timing using MAS setting
You can manually specify exposure timing by setting the mAs value (shown below).
With mAs button selected, the exposure is terminated when the specified mAs value
is reached.
To specify the exposure by mAs, ensure the mAs button in the Exposure Control
panel is selected, then click on the Increase mAs button or Decrease mAs button
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located to the right of MAS value field to set the desired value. The value changes by
one unit each time. Pressing and holding the button causes the value to increase or
decrease automatically until the button is released. If the value reaches maximum or
minimum, the value will remain unchanged.

Figure 45: MAS Setting

With the mAs button selected, the TIME controls are dimmed. Since the TIME
settings and MAS setting are dependent to each other.

Adjusting Exposure timing using TIME settings

You can manually specify exposure timing by setting the mA and the ms value. When
using the TIME settings (shown below), the exposure is terminated when the specified
time value is reached. This mode is used when a specific time must be achieved,
such as in a breathing study or for stop motion. Regarding the reciprocal grid’s
requirement on exposure window, the ms value should be guaranteed above 50 when
the system employs reciprocal Grid.

To specify the exposure by Time setting, make sure the Time button in the
Exposure Control panel is selected (shown below), then click on the Increase
mA/ms button or Decrease mA/ms button to set the desired values. The value
increases and decreases in steps of one unit. Pressing and holding the button causes
the value to increase or decrease automatically until the button is released. If the
value reaches maximum or minimum, the value will remain unchanged.

With the Time button selected, the mAs controls are dimmed. Since the TIME
settings and mAs setting are dependent to each other. Changing mA/ms values
causes the mAs value changes.

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Figure 46: TIME Setting


Selecting the Focal Spot Size
To select the focal spot size, click on the corresponding size button. The selected
button will be pushed down.

Figure 47: Focal Setting

If the selected Focal Spot Size is not compatible with the tube
and focal spot, the system inhibits exposure and displays an
overload condition. An overload condition may exist if the
technique selected exceeds the maximum or is below the
minimum allowable X-ray tube focal spot rating. The tube
parameters are consistent with the X-ray tube manufacturer's
rating charts.

Hardware Status
The status of hardware is displayed in the Common Message area, as shown below.

Figure 48: Hardware Status:OK/ Warning/ Error


Reset Hardware
If there has an error and it cannot auto recover, the error message will remain in
message field.
Click the Reset button before performing subsequent exposure.

Figure 49: Reset button


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5.2.4.4 Checking the Patient and Exposure Information

In Process window, you can see the patient/study information on the top left of the
image, and the real exposure dose information on the top right of the image.

Figure 50: Patient and Exposure Information


Add Markers to an Image
These markers can be used to designate left and right, the position of the patient.

Figure 51: Marker buttons

To add a marker to the image, click on the marker button. The added marker
displays on the top left corner of the image. The added marker could be dragged to
wherever you want on the image within the clipping area.

It is up to four markers and/or comments that could be


added on the image.

Work with Comments


By clicking Define Mark button, you can add a customized label which will be
displayed on the image.

Figure 52: Define Mark button

Click Define Mark button, Labe list displays as the following figure. You can add
information into image by clicking an item from the list.

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Figure 53: Label list


To add a customized label
1. If the label information you want to add is in the predefined list, choose the
associated checkboxes. Otherwise, you have to add the customized comment by this
way: System -> DROC Configuration -> System -> Image Comment, input the
customized commentinto the text field, and then click New button to save it. Now you
could find the new customized comment in the Image Comment list. You can also
delete a current comment by clicking Delete button after select the comment in Image
Comment tab of DROC Configuration page.
2. Click the new customized comment from the Image Comment list to add the
comment. The Image Comment list closes and the comment display(s) on the image
Area of Process window.

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Figure 54: The image with added label

Remove Marks and Comments


Clicking Clear All Marks button, all of added marks and comments are removed from
the image.

Figure 55: Clear All Marks button

View Full Size Image


Click the Original Size button; you can view the image in full size by holding the left
mouse key pressed and moving mouse to desired direction. In Original Size mode
you can only view the image, cannot permitted to clip, rotate and do other operations.
To enable such operations, you must return to Fit Window mode by click Fit Window
button

Figure 56: Fit Window button and Original Size button

Rotating the Image


The image can be rotated 90° (clockwise) or 90° (anti-clockwise) clockwise as
required. It isrecommended that, if the image is rotated, please use markers to
designate either left or right rotation.

Figure 57: Image Rotate buttons

Mirror the Image


The image can be mirrored by clicking Flip Horizontally button or Flip Vertically
button.

Figure 58: Flip Horizontally button and Flip Vertically buttons

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Clip an Image
When an image has been captured and is displayed in the Process window, you can
clipthe image for output to a DICOM print or storage device.
When you accept the image, the full image along with any clipping information, is
stored in the local disk and can be recalled for clipping again within a period of time.
Meanwhile, the clipped image is sent to the DICOM output device.

To display the clip lines: click the Recover Clip button.

Figure 59: Recover Clip button

To remove the clip line and not clip the image: click the Remove Clip button.

Figure 60: Remove Clip button

To fix clip line: click Save Clip button, the current clip line set to be the default clip
line.

Figure 61:Save Clip button

To change clip size: choose one item from the clip size drop-down list which can be
triggered by clicking Define Clip Size button,the items in the drop down list represent
standard film size with inch being unit.

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Figure 62: Clip Size List of Define Clip Size button

Rotate the Image with any angle

To Rotate the image by Rotate Any Angle button, make sure the Rotate Any Angle
button is clicked (shown below), then click the Increase button or Decrease button to
set the desired values. The value increases and decreases in steps of one unit.
Pressing and holding the button causes the value to increase or decrease
automatically until the button is released. If the value reaches maximum or minimum,
the value will remain unchanged.

Figure 63: Rotate Any Angle

Add Mask on the image


If you like to see only part of the image, you can add the mask on the image. Click the
Add/Delete Mask button, click several points around your interested region and
double click the end point. The system will add mask on the image except the setting
region, like following figure.

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Figure 64: Add Mask button and Delete Mask button

Figure 65: Image with mask

Show the image with inversed phase chromatography


If you like to see the inverse image, click the Invert button.

Figure 66: Invert button

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Figure 67: Inversed image

Select LUT or Symphony


The DROC supports both LUT algorithms to adjust the image contrast,and
Symphonyalgorithms to enhance the image based on the anatomy selected. Click the
corresponding button to use the algorithms.

Figure 68: LUT button, Symphony button, Custom Symphony button

Click the LUT, Symphony button or Custom Symphony, system would use the default
parameters to process the image.

Adjust the LUT

When previewing an image, you can modify the LUT settings of the image. The LUT
controls the minimum and maximum densities used in the printed or viewed image.

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When the system is installed, customized default LUT settings are configured for
each procedure type. The image’s original LUT is created by applying the procedure’s
specified LUT settings to the image data.

Typically, you need to change the LUT only for patients with health conditions that
may affect the image quality, such as emphysema for chest views.

To modify an image’s LUT: drag one of the three square handles of the graph line
until the image shows the way you want. If the top or the bottom one is moved out of
display are and is invisible, one the middle one can be dragged. You can also press
and hold the right mouse button, and move the mouse on image preview area to
change the LUT. Vertical movement changes window width of LUT, horizontal
movement changes window level of LUT.

Figure 69: LUT

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5.2.4.5 Outputting Images manually (optional)

After captured, the images will be sent to default destinations or printers automatically.
But you can still re-send the images to different destinations or resend images from
Output window.

There are two types of output destinations: archive server for storage and printer
for printing. These two destinations (may contain zero or multiple nodes) can be
configured for all images belong to the same procedure. Furthermore, the film
orientation, size and format can be configured for each different procedure. When an
exam is opened, these configurations are loaded automatically. You can also change
them manually for current Study .

For more information, please refer to Section D: Working with Worklist Studies.

5.2.4.6 Closing the Study/Patient

You can quit the Exam window to perform other operations, no matter whether all
the images are captured or not.

To quit the Exam window, click the button in Next Step area.

● If all of the images in the current study has being acquired, the status of this
Study will become Completed in Worklist window;
● Otherwise, the status will become In Progress in Worklist window.

You can pick up the incomplete Study from the Worklist window to proceed with the
exposures whenever you like.

The fact that a Study is incomplete does not prevent the patient
record and associated images from being deleted which is part
of the system's storage space reclamation process. For more
information about the reclamation, and how to protect a
patient record and associated images from being deleted,
refer to Section E.When Study is closed and no new patient is
selected, the detector will perform offset calibration; if no Study
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is opened for a period of time, the detector enters “sleep” mode


to save energy. To make detector could enter “sleep” mode
when system is idle, don’t leave a Study opened for a long time
without taking exposure.

5.2.4.7 Logging Off the DROC Application

To log off the DROC application, click the Exit button from the Menu Bar. The DROC
Close dialog displays.

Figure 70: DROC Exit dialog

Three options are available:


● Logoff:Switch to Login window to log in DROC with another user
● Exit:Close DROC
● Shutdown Computer:Power down the PC
5.2.4.8 Power Off the System

Typically, you should leave the system components on. The DROC HOST PC, monitor,
and Detector are able to enter an energy-saving "sleep" mode1 when they are not
used for a period of time.

Recommended Power off Procedure Overview


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To power off the system, it is recommended that you perform the power off tasks in
the following sequence,

Steps:

1. Shut down the DROC HOST PC.


Firstly close all the applications running in PC; then from the Start Menu,
choose “Turnoff the computer” “Turn off”.
2. Power off the X-ray generator.
Powering off the X-ray generator also typically DOES power off the other
X-ray system components, such as X-ray tube, tube suspension arm,
collimator, Bucky , and table (if applicable).

The DROC HOST PC should be shut down once a day to


ensure a complete system reset. If this is not done, system
performance may deteriorate.

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CHAPTER6 MAINTENANCE

6.1 Maintenance the operator can carry out and clean


1. General Rules
This equipment needs regular maintenance; following suggestions will be good for usage and
safety.
● Keep room clean, dry, and with good ventilation.
● Mechanical safety will be degraded due to long time usage. In order to reduce potential
damage to both user and patient, it is necessary to check mechanism if any looses and if
brake is good.
● Correct electrical calibration can well perform machine’s performance.Calibration work
should be completed by professional staff authorized by our company.
● Machine should be in charged by designed person and establish file management system.
● Any changes to machine are forbidden to ensure both patient and operator’s safety, If any
changes needed, please contact with manufacturer.
● Adjustment for contact gap among moving parts with orbital bearing assembly should
be done once a year.
● Regular big repair should be done, for details pls contact with manufacturer.
● If product has malfunction, contact with professional staff approved by manufacturer.
● Operator should be well trained and can complete normal inspection.

2、Maintenance and Repair for unit


(1) Cleaning the surface of the unit , can use soft cloth with a little anhydrous alcohol to
scrub.Organic solution can't be used to scrub the surface of the machine parts absolutely .
(2) Anti-bacterial requested machine surface touched by patients, such as
sterilizing the table panels, can use the ethanol for disinfection, but
mercurochrome,
iodine are not allowed. It is suggested that Ultraviolet radiation etc. is configured
on a
regular disinfection in the machine room.

For the disinfection work, unit power must be shut down! And
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disinfection liquid should be paid attention that it can’t flow into the unit interior, lest the
phenomenon of leakage and short circuit is occured, which will lead to all kinds of malfunction,
even cause injuries.

3、Maintenance and Repair for collimator


(1) Collimator should be kept clean, dry, transmission parts and components shall not
have dust.
(2)After period of time usage, check whether the bar lead-leaf get loose, and fix it
in time ( check it every three to six months).Few thin lubricant can be added
on internal mechanical parts.
(3)When any malfunction is happened , it should be done by professional
person or contact factory in time for maintenance.
4、Maintenance and repair for X-ray tube assembly
(1)、After continuous exposure, it should pay attention to X-ray tube temperature
rise. When the temperature of outer surface components exceed 70 ℃,X-ray
generator must stop loading automatically.
(2)、It should ensure that high-voltage cable plugs, sockets have good contact so
X-ray tube filament is always on, and it can avoid X-ray tube to withstand cold
high-voltage, thus extended x ray tube life.
(3)、When X-ray tube components are used for the first time or idled for a longer
time, it must be progressive loading before X-ray tube used ,and do the
sophisticated test to avoid damaging to the X-ray tube by instantaneous load.
5、Maintenance and repair for high-voltage generator
(1)、It should ensure that high-voltage cable plugs, sockets have good contact so
X-ray tube filament is always on, and it can avoid X-ray tube to withstand cold
high-voltage, thus extended x ray tube life.
(2) 、 After removal of high voltage cable sockets, it should pay attention to the
residual charge, do not touch electrode by hand to avoid electric shocks. If
needed, discharge it first.

Attention: Clean dust on top of high-voltage generator.。

6、Maintenance and repair for tables

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(1)、All surfaces of photography table should be kept clean, dry , and variety of
residues can be scrubbed with a soft cloth dipped with few absolute alcohol
(2)、Regular check if bearing or movement orbit is short of oil .After cleaning , it
should coat with lubricant (grease) in time.
(3)、No flammable liquids, gases near the equipment to prevent explosion.
(4)、Protect grounding facilities, and inspections should be done every half year.
(5)、Diagnostic table’s sterilization method are same as the unit’s.

6.2 Maintenance that can be carried out and cleaned by the


Authorised Technician
PLD7200 Medical diagnostic X-ray generator is sophisticated, valuable medical
diagnostic equipment. It is necessary that user’s knowledge about machine’s
technical performance, structure principle, operating procedure and daily
maintenance to give full play to the efficiency of the machine , prolong the useful life of
the machine, ensure the normal use of equipment, ensure the safety of operators and
personnel inspected.
1、Properly operating in the process of using X-ray machine, make its normal
operation, and what’s more important is that it should pay special attention to the
body of X-ray protection, make X-ray operator and the patient's damage down to a
minimum. For example machine room should have protective equipment and
measures (e.g., lead plate), the operator must use protective appliances (such as
lead glasses) and wear protective clothing (lead cap lead, lead aprons,
gloves) ,operator should be occupied area in effective operation when the patients
with radiation inspection .
2、This machine should be placed in air circulation, clean and dry work condition. It
can not be placed in the humidity, heat and sunlight exposure area.
3、Control cabinet should be opened front and back cover regularly (depending on the
environment, such as the six months to one year), and removed internal dust.For
damaged parts, purchase the same model of spare parts from factory for replacement.
During examination, pay attention whether there is any loose terminals and
displacement phenomena, and fasten them.
4 、 In area where the power supply and voltage has a high fluctuation, always pay
attention to whether power supply and voltage is in permitted range.If it has high,
low, mutation and other anomalies, machine should be closed immediately and
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check out the problem, it can only be used after problem solved.
5、 Do not press heavily on all buttons of controller to avoid dislocation, injury or poor
contact, even damaged.
6 、 Check frequently protective earth of each components is in good condition
(grounding resistance is very small).
7、Check power supply on a regular basis, and check power supply resistance value
(or the power supply voltage value is changed), to make sure it meet machine’s
requirement.
8、After using the controller, it should be cut off the power in time.
9、Avoid striking of x-ray tube components during operation.
10、 When X-ray tube components are used for the first time or idled for a longer time,
it must be progressive loading before X-ray tube used ,and do the sophisticated
test to avoid damaging to the X-ray tube by instantaneous load.
11 、 When machine works continuously, please pay attention to the X-ray tube
assembly to allow Thermal capacity, or check surface temperature of X-ray tube
assembly , it can’t exceed 70 ℃.

The personnel for the above inspection, maintenance and


processing must be accredited by professionals; It’s not
allowed for other people to carry out such inspection,
maintenance and processing.
6.3 The cycle of maintenance and repair
Time Interval Contents of Maintenance and inspection

Check if the signal, display and indicator are normal.


Check if warming and danger SYMBOLS are good.
Daily
Check if X-ray generator components has abnormal noise
Inspection during exposure.
Check if all grounding are good.
Check if there is any loose, stuck on the button of the
Console.

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Check if any oil leakage of the X-ray generator component.


Weekly Check flexibility of table and column bearing, observe if any
friction is too large , and coat bearing orbit with lubricating oil.
Inspection Check if any loose and shedding of fastener parts between
components, if any ,should be fixed them in time .

Check machine grounding resistance (less than 0.2Ω).


Check if any filler come out of head of the HV cable because
Check every of heating.
Clear silicone oil on high-voltage outlet, scrub High voltage
six month plugs and sockets with ether or carbon tetrachloride, and
then smear some new silicone grease, tighten the fixing ring
of plug.
Check the centre of X-ray generator assembly and collimator.

6.4 Fault Code and Failure Removal

1 .Diagnostic Table
Fault
Adjustment method
Code
EROR0 Touch screen displays cue

EROR1 Touch screen displays cue

EROR2 Touch screen displays cue

EROR3 Touch screen displays cue

2.HV Generator
Fault
information problem Adjustment method
Code
Consult your service
E001 GEN EPROM ERR representative.

Consult your service


E003 GEN NVRAM ERR representative.

E004 GEN RTC ERROR Generator CPU real Reset time and date.
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time clock doesn't Consult your service
work. representative.
Consult your service
E005 PS CONTACT ERR
representative.
Power unit off and retry rotor
start.
E006 ROTOR FAULT
Consult your service
representative.
Consult your service
E007 FILAMENT FAULT
representative.
Consult your service
E008 KV/MA FAULT
representative.
Power supply is not Retry exposure.
E009 PS NOT READY ready to make an Consult your service
exposuer representative.
Consult your service
E010 LOW KV FAULT
representative.
Consult your service
E011 HIGH MA FAULT
representative.
Consult your service
E012 LOW MA FAULT
representative.
Re-take exposure if
Operator released
necessary .
E013 MANUAL TERMIN exposure switch
Consult your service
during exposure .
representative.
Check exposure
AEC exposure technique settings.
E014 AEC BUT ERROR exceeded Consult your service
allowed back up time. representative.

Check exposure
AEC exposure
technique settings.
exceeded
E015 AEC BUT ERROR Consult your service
allowed back up mAs.
representative.

Tomo exposure
Check exposure
exceeded back-up
E016 TOMO BUT ERROR technique settings.
time.

Consult your service


E017 NOT CALIBRATED
representative.
Generator has been in Reduce length of time in prep
E018 PREP TIMEOUT
prep state too long. state.
E019 ANODE HEAT Selected parameters Reduce parameters or wait
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LIMIT will cause X-Ray tube for tube to cool.


to exceed its
programmed anode
heat limit.
X ray tube # 1
overheating, the Waiting for X ray tube # 1
E020 THERMAL INT #1
overheat switch cooling.
disconnected.
X-Ray tube # 2 too
THERMAL INT #2 Waiting for X ray tube # 2
E021 hot and its thermal
cooling.
switch has opened.
E022 DOOR INTERLOCK Door is open. Close door
Collimator is not
E023 COLLIMATOR ERR. Check collimator.
ready.
E024 CASSETTE ERROR Cassette is not ready. Check cassette.
Spare input is not Consult your service
E026 SPARE INT.
ready. representative.
Consult your service
E028 PREP SW CLOSED
representative.
Consult your service
E029 XRAY SW CLOSED
representative.
Generator has
detected Turn power off and
CONSOLE COMM
E032 error in then on to reset
ERR
communication to generator.
console.
GEN BATTERY Consult your service
E033
LOW representative.
Consult your service
E034 +12VDC ERROR
representative.
Consult your service
E035 -12VDC ERROR
representative.
Consult your service
E036 +15VDC ERROR
representative.
Consult your service
E037 -15VDC ERROR
representative.
Consult your service
E038 CAL DATA ERROR
representative.
Consult your service
E039 AEC DATA ERROR
representative.
Consult your service
E041 REC DATA ERROR
representative.
E042 TUBE DATA ERR. Consult your service
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representative.
Switch OFF
generator. Prevent
further use of
E043 KV ERROR
generator, then.
consult your service
representative.
Received
communication
E044 COMM ERROR Reset error.
message not valid and
ignored.
Received message is
valid,
E045 NOT SUPPORTED but not supported by Reset error.
this
system.
Attempting to change
CM
thickness in AEC
mode if
the receptor is not Consult your service
E046 MODE INHIBITED programmed for mAs representative.
backup. Reset error.
Received message is
valid,
but not allowed during
present state.
Consult your service
E048 FOCUS MISMATCH
representative.
Requested function
has not
Consult your service
E049 NOT ENABLED been programmed to
representative.
be
enabled.
Consult your service
E050 GEN DATA ERROR
representative.
Generator has Check that X-Ray
detected no tube is pointing at
E051 AEC DEVICE ERR feedback signal from correct AEC device.
AEC Consult your service
device. representative.
Consult your service
E052 HIGH SF CURRENT
representative.
E053 HIGH LF CURRENT Consult your service

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representative.
AEC OUT OF Consult your service
E054
RANGE representative.
AEC enabled but no
E055 NO FIELDS ACTIVE fields Select AEC field(s).
are selected.
NO TUBE Consult your service
E056
SELECTED representative.
Consult your service
E057 AEC STOP ERROR
representative.
CONSOLE BUT Consult your service
E058
ERR. representative.
X-Ray tube housing
HOUSE HEAT
E059 has Wait for tube to cool.
LIMIT
exceeded limit.
Consult your service
E060 EXP. KV HIGH
representative.
Consult your service
E061 EXP. KV LOW
representative.
Consult your service
E062 EXP_ SW ERROR
representative.
FACTORY Consult your service
E063
DEFAULTS representative.
Generator duty limit Consult your service
E067 PS DUTY LIMIT
reached. representative.
MAS OVERTIME Consult your service
E069
ERR representative.
SOFTWARE KEY Consult your service
E070
ERR representative.
The accumulated DAP
Reset the DAP.
DAP DOSE value exceeds the
E071 Consult your service
OVERFLW display
representative.
limit.
The DAP device is not Consult your service
E072 DAP DEVICE ERR.
functional. representative.
Consult your service
E073 DAP DATA ERROR
representative.
INVERTER 1 Consult your service
E074
ERROR representative.
INVERTER 2 Consult your service
E075
ERROR representative.
INVERTER 3 Consult your service
E076
ERROR representative.
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Consult your service
E077 RES. CIRCUIT ERR
representative.
BUCKY1 Consult your service
E078
INTERLOCK representative.
BUCKY2 Consult your service
E079
INTERLOCK representative.
INTERLOCK 1 Consult your service
E080
OPEN representative.
INTERLOCK 2 Consult your service
E081
OPEN representative.
KV OVER Consult your service
E082
VOLTAGE representative.
Consult your service
E083 ANODE MA FAULT
representative.
CATHODE MA Consult your service
E084
FAULT representative.
ROTOR MAIN Consult your service
E085
FAULT representative.
ROTOR SHFT Consult your service
E086
FAULT representative.

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CHAPTER7 ATTACHMENT

7.1 Spare parts list

Quantit
NO Name Unit
y
1 Fuse(380V/16A): pcs 3

2 Fuse(220V/2A): pcs 2

3 Fuse(220V/5A): pcs 1

Packing: Check: Date:

Company: Nanjing Perlove Medical Equipment Co., Ltd. Tel: 025-87187780

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7.2 Safety Performance Inspection Report
1. Electrolyte strength under normal working temperature
Test condition: AC Voltage 1500V Time 1 min
Conclusion:

2 .Grounding resistance
Protective earthing and protective grounding of all possible resistance between the metal parts
touch, maximum: Ω<0.1Ω
Conclusion:

3. Continuous leakage under normal working temperature


Normal state:
Earth leakage: outside leakage: patient leakage:

Single fault state:


Earth leakage: outside leakage: patient leakage:

Conclusion:

Test stuff: Date:


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7.3 Packing list

Packing list(1)
NO Name Unit Quantity
1 Radiographic table pcs 1
2 Grid (South Korea) Pcs 1
3 Collimator (auto/ manual) Pcs 1
4 Console Pcs 1
5 Connection wires: Pcs
XJZ00-01 generator control wire Pcs 1
XJZ00-02 PLC-EVIEW communication cable Pcs 1
XJZ00-03 boot, brake, CCD, EVIEW power wire pcs 1
XJZ00-04 console control cable pcs 1
XJZ00-05 brake, image intensifier, foot switch, motor pcs 1
cable
XJZ00-06 collimator, load indicator cable pcs 1
XJZ00-07 cassette motor cable pcs 1
XJZ00-08 table control signal cable pcs 1
XJZ00-10 ground wire Pcs 7
XJZ00-11 Radiographic table power cable Pcs 1
XJZ00-12 heat protection and rotary anode wire Pcs 1
XJZ00-15 speaker wire 2 Pcs 1
XJZ00-17 microphone wire pcs 1
XJZ00-19 speaker wire 1 pcs 1
XJZ00-20 cassette AD wire pcs 1
XJZ00-05A three-phase AC motor line pcs 1
XJZ00-23 video cable Pcs 2
XJZ00-35 In the control of power cable Pcs 1
ZDC20-02 the Collimator lamp wire Pcs 1
ZDC20-04 Radiographic table internal magazine signal pcs 1
cable
X-ray tube components pcs 1
Image Intensifier pcs 1
High voltage generator(CPI) pcs 1

6
7
8

Packing: Check: Date:


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Company: Nanjing Perlove Medical Equipment Co., Ltd. Tel: 025-87187780

packing list(2)

NO Name Unit Quantity


1 Generator control panel Pcs 1
2 High voltage cable(12m) Pcs 2
3 Radiography system pcs 1
4 Monitor pcs Optional
5 Speaker pcs 2
6 control cabinet pcs 1
7 Touch screen pcs 1
8 digital workstation pcs 1

Packing: Check: Date:

Company: Nanjing Perlove Medical Equipment Co., Ltd. Tel: 025-87187780


119

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