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ARCADIS Varic
SP

Startup
System

Start-up Instructions

08080017

© Siemens AG 2006
The reproduction, transmission or use
of this document or its contents is not
permitted without express written
authority. Offenders will be liable for
damages. All rights, including rights
created by patent grant or registration
of a utility model or design, are
reserved.

Print No.: SPR2-310.815.01.07.02 English

Replaces: SPR2-310.815.01.06.02 Doc. Gen. Date: 12.06
2 Revision / Disclaimer
1Revision / Disclaimer

Document revision level

The document corresponds to the version/revision level effective at the time of system
delivery. Revisions to hardcopy documentation are not automatically distributed.
Please contact your local Siemens office to order current revision levels.

Disclaimer
The installation and service of equipment described herein is to be performed by qualified
personnel who are employed by Siemens or one of its affiliates or who are otherwise
authorized by Siemens or one of its affiliates to provide such services.
Assemblers and other persons who are not employed by or otherwise directly affiliated
with or authorized by Siemens or one of its affiliates are directed to contact one of the
local offices of Siemens or one of its affiliates before attempting installation or service pro-
cedures.

ARCADIS Varic SPR2-310.815.01.07.02 Page 2 of 64 Siemens AG

12.06 CS PS SP Medical Solutions
Table of Contents 3
0Table of Contents

1 _______ General information______________________________________________ 5

Notes and symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Additionally required documents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Safety information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
General safety information (in existing documents) . . . . . . . . . . . . . . . . . . . . . . . . . . 8
General electrical safety information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Radiation safety information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Systems equipped with an I.I. laser light localizer or a single tank laser light localizer 9
Systems equipped with an integrated I.I. laser light localizer . . . . . . . . . . . . . . . . . . 10
Information on the protective conductor resistance test . . . . . . . . . . . . . . . . . . . . . . 11
System leakage current measurement information . . . . . . . . . . . . . . . . . . . . . . . . . 13
Tools, aids (partially for IQ test) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Note on the log book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Notes on adapting the power plug to local conditions. . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Power line connection information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

2 _______ General Start-up________________________________________________ 23

Power connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Measuring the local line voltage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Adjusting the programmed system line voltage . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Function check of the emergency stop switches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Checking the temperature indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Function checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Functional test of C-arm lift movement and parking brakes . . . . . . . . . . . . . . . . . . . . . . 28

3 _______ Specific system settings_________________________________________ 29

System configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Note regarding Hibernation Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Customer and country-specific configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Service login . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Customer address configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Main system configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Country-specific adaptation of the maximum tube current . . . . . . . . . . . . . . . . . . . . 36
Configuring the network (optional) and remote service . . . . . . . . . . . . . . . . . . . . . . 39
Backup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40

4 _______ Final Work Steps _______________________________________________ 44

Paper printer (optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Codonics printer 1660L. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Sony printer UP-D72 X . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Sony Printer UP-970 and UP-990. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Final work steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
IQ test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Completing protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

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4 Table of Contents

Protective conductor resistance test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Leakage current measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Completing the "ARCADIS Varic Installation" protocol . . . . . . . . . . . . . . . . . . . . . . . 50

5 _______ Protocols______________________________________________________ 51

Protective conductor resistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51

Measuring circuit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Comments: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
System leakage current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Measuring circuit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Comments: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
C-arm movement and emergency stop. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Network checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

6 _______ Changes to previous version _____________________________________ 64

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12.06 CS PS SP Medical Solutions
General information 5
1-
Notes and symbols
1General information

Emphasized text in this technical documentation has the following meanings:

Tab. 1 GEFAHR / DANGER

Bei einer unmittelbar drohenden Gefahr, die bei Nichtvermeidung

zum Tod oder zu einer schweren Körperverletzung führt.

Indicates when there is an immediate danger that leads to death

or serious physical injury.

Tab. 2 WARNUNG / WARNING

Bei einer Gefahr, die bei Nichtvermeidung zum Tod oder zu

einer schweren Körperverletzung führen kann.

Indicates a risk of danger that may lead to death or serious phys-

ical injury.

Tab. 3 VORSICHT / CAUTION

Bei einer Gefahr, die bei Nichtvermeidung zu einer leichten oder

mittleren Körperverletzung und/ oder zu einer Sachbeschädi-
gung führt oder führen kann.
Indicates a risk of danger that leads to slight or moderate physi-
cal injury and/or damage to property.

Tab. 4 ACHTUNG / NOTICE

Bei einer Gefahr, die bei Nichtvermeidung zu einem unerwünscht-

en Ergebnis oder Zustand führt oder führen kann (nicht Tod,
Körperverletzung oder Sachbeschädigung).
Indicates a risk of danger that if disregarded leads or may lead to
a potential situation which may result in an undesirable result or
state (not death, physical injury or property damage).

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6 General information
Tab. 5 HINWEIS / NOTE

Ist als Tipp zu verstehen. Der Anwender muss diese Anweisung

nicht unbedingt beachten. Er erfährt jedoch Vorteile, wenn er
dies tut.
Should be understood as a tip. The user does not absolutely
have to observe these instructions. However, there will be
advantages if he does.

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12.06 CS PS SP Medical Solutions
General information 7

Additionally required documents 1.1

• ARCADIS Varic operating instructions

• ARCADIS Varic system wiring diagram
• IQ test (quality assurance)
• Local printer (optional) assembly and setting instructions
• Image intensifier laser light localizer (optional) assembly and setting instructions
• Single tank laser light localizer (optional) assembly and setting instructions

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8 General information

Safety information 1.2

General safety information (in existing documents) 0

WARNING Danger of injuries, death or material damage.

Non-compliance can lead to death, injury or material damage.

Please note:
¹ The product-specific safety information in these instruc-
tions,
¹ The general safety information in TD00-000.860.01... and
¹ The safety information in accordance with ARTD Part 2.

General electrical safety information 0

WARNING Electrical safety!

Non-compliance can lead to severe injury or even death, as well
as material damage.
¹ Parts under electrical voltage are accessible when the
covers are open. To avoid danger, disconnect the system
from the power supply before opening the covers. Dis-
connect the power plug.
¹ If an uninterruptible power supply (UPS) is installed in
the system, the voltage output of the UPS must also be
deenergized or the voltage output plug must be discon-
nected.
¹ If work steps must be performed using electrical power,
the general safety information according to
TD00-000.860.01... must be observed.

Main system control board D1 and power board D2

WARNING Danger high voltage!

When the system is switched off, there is still electrical voltage on
boards D1 and D2 of the main system.
Disregarding safety precautions can result in death or serious
bodily injury.
¹ Therefore before working on one of these boards, make
sure that the LED V400 has gone out. This is the case 3
minutes after the ARCADIS Varic system is switched off.

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12.06 CS PS SP Medical Solutions
General information 9

Radiation safety information 0

WARNING X-ray radiation!

Non-compliance can lead to illness, irreversible damage to body
cells and the genotype, severe injury and even death.

During work on the system in which radiation must be released,

the radiation protection directives and the rules for radiation pro-
tection according to ARTD-002.731.02.. must be complied with.
Please note:
¹ Use available radiation protection devices.
¹ Wear radiation protection clothing (lead apron).
¹ Stay as far away as possible from the radiation source.
¹ Release radiation only if necessary.
¹ Set the radiation activity as low as possible. (low kV and
mA values, short radiation time)
¹ Release radiation for as short a time as possible.
X ¹ Checks requiring the release of radiation are identified by
the radiation warning symbol shown on the left.

Systems equipped with an I.I. laser light localizer or a single tank laser light
localizer 0

CAUTION Laser emissions!

This product contains class 2 lasers. (USA: Class 2 laser)
Disregarding safety precautions can lead to bodily injury, espe-
cially to the retina of the eye, resulting in irreversible damage to
vision.
¹ Observe the safety information in ARTD-002.731.03...
When working with the laser light localizer, do not look
directly into the laser beam.

NOTE Laser emissions!

There is no direct hazard to the eye (blinking reflex). Nevertheless
do not look directly into the laser beam.

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10 General information

Systems equipped with an integrated I.I. laser light localizer 0

CAUTION Laser emissions!

This product contains lasers of the class 1M.
Disregarding safety precautions can lead to bodily injury, espe-
cially to the retina of the eye, resulting in irreversible damage to
vision.
¹ Observe the safety information in ARTD-002.731.03...
When working with the laser light localizer, do not view
the laser beams directly with optical instruments.

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General information 11

Information on the protective conductor resistance test 0

Observe the instructions in the "Safety Rules for Installation and Repair"
(ARTD-002.731.17 ...).
The protective conductor resistance of 0.2 ohms must not be exceeded.
First measured value
In the case of systems thoroughly tested at the factory prior to delivery, the protective con-
ductor resistance test was already performed and the measured values were recorded in
the system test protocol.
The measurements were performed using the measuring procedures and measuring
equipment recorded in the system test protocol.
The test protocol is included with the accompanying documentation.
If no covers were opened while installing the system and no additional components (e.g.
options) were installed or modified, the values recorded in the test protocol including the
measuring point (e.g. cover of the basic unit or cover of the image intensifier) can be
transferred to the protective conductor resistance protocol as the first measured values.
If the power plug was changed during system installation, covers were removed, or addi-
tional components were installed or modified, the values provided in the test protocol are
invalid.
The values must be labeled invalid. Cross out the values, enter the comment "invalid
value" and confirm this with name, date and signature.
The protective conductor test must be performed again after all work has been completed.
In the case of systems with no measured values for the protective conductor test recorded
in the system test protocol, the protective conductor test must be performed after all work
has been completed.

Measurement
The measurement must be performed in accordance with DIN VDE 0751, Part 1 (refer to
ARTD Part 2). The protective conductor resistance for all touchable conductive parts must
be measured during the normal operating state of the system.

Make sure that control cables or data cables between the system components are not
mistaken for protective conductor connections.

During the measurement, the power cable and additional connection cable with the inte-
grated protective conductor (e.g., monitor cable between the basic unit and monitor cart)
must be moved section by section to detect cable breaks.
The protective conductor resistance must not exceed 0.2 ohms.

The values, including the measuring points, must be recorded as first measured values in
the protective conductor resistance protocol.

The measuring procedure and the measuring device used (designation and serial num-
ber) must also be documented.

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Medical Solutions 12.06 CS PS SP
12 General information

Separate the page with the protocol from these instructions and file it in the "Protocols"
register in the system binder or log book.

Fig. 1: Measuring circuit for measuring the protective conductor resistance for units that are

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12.06 CS PS SP Medical Solutions
General information 13
disconnected from power, in compliance with DIN VDE 0751-1/2001-10, Fig. C2.
Pos. 1 = System
Pos. 2 = Application part type B (if available)
Pos. 3 = Measurement setup (integrated into measuring device)

Repeat measurement
In the case of maintenance or repairs, perform the protective conductor resistance mea-
surement again.
Document and evaluate the values determined in the repeat measurement.
The measurement must be performed in accordance with DIN VDE 0751, Part 1 (refer to
ARTD Part 2). The protective conductor resistance for all touchable conductive parts must
be measured during the normal operating state of the system.

Make sure that control cables or data cables between the system components are not
mistaken for protective conductor connections.

During the measurement, the power cable and additional connection cables with the inte-
grated protective conductor (e.g. monitor cable between the basic unit and monitor cart)
must be moved section by section to detect cable breaks.
The protective conductor resistance must not exceed 0.2 ohms.

The values determined in the repeat measurement, including the measuring points, must
be recorded and evaluated in the protective conductor resistance protocol.

The measuring procedure and the measuring device used (designation and serial num-
ber) must also be documented.

NOTE For evaluation purposes, the first measured value and the values
documented during previous maintenance or safety checks must
be compared to the measured values. A sudden or unexpected
increase in the measured values may indicate a defect in the pro-
tective conductor connections (protective conductor or contacts)
- even if the limit value of 0.2 ohms is not exceeded.

System leakage current measurement information 0

Observe the instructions in the "Safety Rules for Installation and Repair"
(ARTD-002.731.17 ...).

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14 General information

WARNING Electrical voltage!

Non-compliance can lead to severe injury and even death.
¹ The system leakage current measurement may be per-
formed on systems of protection class I only after the
protective conductor test has been passed.

First measured value

In the case of systems thoroughly tested at the factory prior to delivery, the system leak-
age current measurement was already performed at the factory and the measured value
was recorded in the system test protocol.
The measurement was performed using the line voltage and line frequency, the measur-
ing procedure, and the measuring equipment recorded in the system test protocol.
The test protocol is included with the accompanying documentation.
When the line voltage and line frequency match, the value recorded in the test protocol
must be used as the first measured value in the system leakage current protocol.
If the local line voltage or line frequency differs from the delivery state of the system or if
no measurement was performed and recorded at the factory, the system leakage current
must be measured.

If the local line voltage or line frequency differs from the delivery state of the system, the
values listed in the test protocol are invalid.
The values must be labeled invalid. The reason for newly determining the first measured
value must be documented and confirmed with date, name, and signature.

Adjust/program the system to the local line voltage/line frequency before the measure-
ment.
In the case of systems with no measured values for the system leakage current measure-
ment recorded in the system test protocol, the system leakage current measurement must
be performed after all work has been completed.
Measurement
Perform the measurement according to DIN VDE 0751, Part 1 (see ARTD-002.731.17....),
and record the determined value as the first measured value.
Measurement of the system leakage current according to the differential current method
(measurement setup according to (Fig. 2 / p. 15)) must be given preference, since this
method is not dangerous to the person performing the measurement and other persons.
However, please note the minimum resolution of the system leakage current measuring
device and any additional manufacturer information restricting the use of the measuring
device.

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General information 15

Fig. 2: Measuring circuit for measuring the system leakage current according to the differential
current method in compliance with DIN VDE 0751-1/2001-10, Fig. C6 for protection
class I.
Pos. 1 = System
Pos. 2 = Application part type B (if available)
Pos. 3 = Measurement setup (integrated into measuring device)

If the direct measurement of the system leakage current is used (measurement setup
according to (Fig. 3 / p. 15)), the system must be insulated during the measurement and
must not be touched.

Fig. 3: Measuring circuit for direct measurement of the system leakage current in compliance

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16 General information
with DIN VDE 0751-1/2001-10, Fig. C5 for protection class I.
Pos. 1 = System
Pos. 2 = Application part type B (if available)
Pos. 3 = Measurement setup (integrated into measuring device)

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12.06 CS PS SP Medical Solutions
General information 17

WARNING Electrical voltage!

Non-compliance can lead to severe injury and even death.
¹ No housing parts of the system may be touched during
direct measurement of the system leakage current (mea-
surement setup according to (Fig. 3 / p. 15)).
¹ Third-person access to the system must be prevented.

The system must be switched on during measurement. Measuring devices with auto-
mated measuring sequences must therefore be set to manual measurement.

Enter the highest value as the first measured value in the system leakage current proto-
col.

This value must not exceed the permissible leakage current values according to DIN VDE
0751-1/2001-10, Table F.1, line "system leakage current for units according to remarks 1
and 3" of
2.5 mA.

Measure and record the current line voltage. If the measured line voltage deviates from
the nominal voltage, correct the measured value to the value corresponding to a measure-
ment at the nominal value of the line voltage. This must also be documented.
Document the measuring procedure (differential measurement or direct measurement)
and the measuring device used (designation and serial number).

Separate the protocol sheet from these instructions and attach it to the protocols already
in the system binder or log book.

Repeat measurement
When maintenance or repair work is performed on the primary power supply circuit (e.g.
repairs to the power-on circuit or replacement of the line filter), the system leakage current
measurement must be repeated.
The same measuring conditions as in the first measurement apply.
Record and evaluate the highest value determined in the repeat measurement in the
existing system leakage current protocol.
This value must not exceed the permissible leakage current values according to DIN VDE
0751-1/2001-10, Table F.1, line "system leakage current for units according to remarks 1
and 3" of
2.5 mA.
Measure and record the current line voltage. If the measured line voltage deviates from
the nominal voltage, correct the measured value to the value corresponding to a measure-
ment at the nominal value of the line voltage. This must also be documented.
Document the measuring procedure (differential measurement or direct measurement)

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18 General information

and the measuring device used (designation and serial number).

NOTE For evaluation purposes, the first measured value and the values
documented during previous maintenance or safety checks must
be compared to the measured values. A sudden or unexpected
increase in the measured values may indicate that a fault has
occurred in the primary power supply circuit (insulation damage,
damage from moisture, defective interference suppressor, etc.) -
even if the limit value of 2.5 mA is not exceeded.

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General information 19

Tools, aids (partially for IQ test) 1.3

• Tool case 97 02 457 Y1971

• Dynamic test case 37 90 156 X1963
• Copper filter set 44 06 120 RV090
• Densitometer 97 02 416 Y1996
• Radiation filter set (incl. 25 mm Al) 97 98 596 G5321
• Resolution test 28 71 820 RE999
• Safety tester (leakage current and ground wire testing device) 51 38 727 Y0766
e.g. Unimed 1100

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20 General information

Note on the log book 1.4

The log book is located in the monitor cart behind the keyboard. It is accessible if the
cover on the back of the monitor cart is removed.

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12.06 CS PS SP Medical Solutions
General information 21

Notes on adapting the power plug to local conditions. 1.5

The customer can have the power plug on the supplied power cable replaced with an
appropriate local plug by an electrician, provided that:
• The power plug used can conduct the power required for the operation of the ARCADIS
Varic (refer to current and voltage values stated on the line voltage label, back of moni-
tor cart).
• The required line internal resistance is reached (refer to ARCADIS Varic Planning
Guide).
• The selectivity of the fuse protection is assured - according to the relevant national
standards.
It must also be ensured by the customer that connection to an unsuitable power supply is
prevented (e.g. by identification or design measures).
As concluding measures, perform and document protective ground wire measurements
(in Germany e.g. in the medical device book).

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22 General information

Power line connection information 1.6

The delivery state of the system with respect to the power line connection values is indi-
cated by the line voltage label or in the operating instructions.
Any necessary adjustments to local conditions must be performed in accordance with the
service instructions/the circuit diagram of the system.
The system leakage current measurement guidelines must be observed.

WARNING Electrical voltage!

Non-compliance can lead to severe bodily injury and even death.
¹ The internal uninterruptible power supply of the system
(UPS) provides several components with line voltage -
even when the system is switched off or the system
power plug is disconnected.
¹ Before the system is programmed to the local line volt-
age/line frequency, it must be disconnected from the
power supply (the power plug must be disconnected)
and the voltage output plug of the UPS must be discon-
nected as well.

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General Start-up 23
2-
Power connection
2General Start-up

Measuring the local line voltage 0

• Measure the voltage and frequency at the intended outlet for the ARCADIS Varic sys-
tem.
• Compare the measured line voltage with the line voltage label on the back of the moni-
tor cart.
¹ The measured voltage (+/- tolerance) must agree with the voltage read off from
the label.

Adjusting the programmed system line voltage 0

NOTE Only perform if the local line voltage does not match the pro-
grammed line voltage of the delivered system.

NOTE After adjustment of the line voltage, the leakage current values
logged in the system test protocol are no longer valid.
After all covers have been closed and the protective conductor
test has been successfully completed, the system leakage current
measurement must be repeated and documented.
Observe the leakage current measurement instructions in the
"General information" chapter of these instructions.

WARNING Danger high voltage!

Disregarding safety precautions can result in death or serious
bodily injury.
¹ Before the line voltage is adapted, the power plug on the
UPS in the monitor cart must be disconnected, since the
monitor cart is not free of voltage after the power plug is
pulled out.

• Remove the back, bottom covers (Fig. 4 / p. 24) from the monitor cart.
• Pull the power plug out of the UPS in the monitor cart.
• Adapt the voltage by changing the connections to transformers T1 and T2. Refer to the
ARCADIS Varic wiring diagram.

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Medical Solutions 12.06 CS PS SP
24 General Start-up

Fig. 4: Monitor cart line voltage

Pos. 1 Power plug
Pos. 2 T1 and T2

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12.06 CS PS SP Medical Solutions
General Start-up 25

Function check of the emergency stop switches 2.1

• Connect the system to the voltage and boot it.

• Click "Emergency" for the patient registration.
• Operate the EMERGENCY STOP switch on the C-arm.
• The safety switch moves audibly and the following message appears on the lower left
monitor edge: "The emergency stop has been pressed"
• Disengage the EMERGENCY STOP switch.
• The safety switch moves audibly and the following message appears on the lower left
monitor edge: "The emergency stop switch has been released."
• Document the function of the EMERGENCY STOP switch in the "Test protocol, C-arm
movement and emergency stop.

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26 General Start-up

Checking the temperature indicator 2.2

• Check the temperature indicator on the outside of the image intensifier housing.
¹ If the inner, square field of the indicator is white, the temperature has not been
exceeded. Remove the temperature indicator.
¹ If the indicator is discolored (inner field black), proceed according to IQ docu-
ment RXD0-000-038.01.xx.xx.

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General Start-up 27

Function checks 2.3

Operation of the ARCADIS Varic, see operating instructions

• Stand and C-arm system movements
X • Semi-transparent slot and iris diaphragm in fluoroscopy procedure.

X • Collimation of the semi-transparent slot and iris diaphragm using fluoroscopy proce-
dure.
• Mechanical functions of the monitor cart

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Medical Solutions 12.06 CS PS SP
28 General Start-up

Functional test of C-arm lift movement and parking brakes 2.4

Fig. 5: C-arm movement functional test

• Switch on the main system (C-arm).
• To move the C-arm downward, press the downward button.
• The lifting column moves to position 1 (1/Fig. 5 / p. 28) and remains there automati-
cally. A stop signal (3 beeps) sounds simultaneously.
• To lower the lifting column further, press the downward button once again.
• The lifting column can then be moved by a further 5 cm to the lowest point, position 2
(2/Fig. 5 / p. 28). In this area a signal (3 beeps) sounds for safety reasons each time the
downward button is pressed.
• To move the C-arm upward, press the upward button. No signal sounds in this case.
• The lift motor remains stationary if both buttons are pressed simultaneously.
• Loosen the different parking brakes and apply them again. Secure blocking of the rele-
vant movement must be assured.
• Document the function of the C-arm movements, brakes and warning signals in the test
protocol, "C-arm movement and emergency stop" .

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12.06 CS PS SP Medical Solutions
Specific system settings 29
3-
System configuration
3Specific system settings

Note regarding Hibernation Mode 0

NOTE Hibernation Mode

With the introduction of the Hibernation Mode, system configura-
tion changes are not applied if the system is switched off and
then switched on again using the power buttons on the monitor
cart.
To correctly apply the modified data, perform a system shutdown.
Open the <Options> - <End Session> menu and click the “Shut-
down system” button. Immediately thereafter, press the Power off
button on the monitor cart.
The system shuts down and switches off automatically.

Customer and country-specific configurations 0

• Please clarify in advance with the customer whether the following system configura-
tions are required.

Service login 0

Fig. 6: Service login

• Click on <Options> <Customer service> <Local service>.

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30 Specific system settings

Fig. 7: Authentication_
• Enter the 6-character password and click OK (see system folder for password).

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Specific system settings 31

Customer address configuration 0

Fig. 8: Configuration_
• Click on <Configuration>.

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Medical Solutions 12.06 CS PS SP
32 Specific system settings

Fig. 9: Configuration
• Click <Next>.

Fig. 10: Configuration_Local Host

• Click <Site Info>.

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Specific system settings 33

Fig. 11: Configuration_Local Host_Site Info

• The marked customer-specific data may be adapted. Under no circumstances may you
change the "serial no." or "station name".
• Click <Save>.
• Click <Home>.

Main system configuration 0

• Start the service program and log in as described under "Service Login".

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34 Specific system settings

Fig. 12: Main_system

• Click <Main system>.

Fig. 13: Main system_

• Select ARCADIS Varic and click <Next>.

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Specific system settings 35

Fig. 14: Main System_Configuration_Buzzer

• Under Configuration click <Buzzer>.

Make changes according to the following description:

• Block time settings
- Warning time limit: The buzzer sound starts when the entered radiation time has
elapsed.
- Block time limit: After the entered radiation time has elapsed - without reset of the
“warning time limit" - the radiation is blocked the next time it is selected. Every reset
of the “warning time limit” also resets the “block time limit” to “0”.
• Buzzer mode (direct, cassette)
- After exposure:Buzzer sound after the exposure.
- During exposure:Buzzer sound during the exposure.
• Buzzer mode (indirect, I.I.)
- Buzzer off:Buzzer sound off. Exceptions: Push mode and “warning time limit” has
ended.
- Buzzer on: Buzzer sound always during radiation.
The country-specific regulations must be observed for the max. fluoroscopy time and the
radiation blockage.
Factory setting:

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36 Specific system settings

"Warning time limit" "Blocking time limit"

USA
5 min. 0 min.
Service mask
50 0
input in 1/10 min.
Europe
5 min. 10 min. (5 min. + 5 min.)
Service mask
50 50
input in 1/10 min.

• Make country-specific changes and click <Save>.

• Click <Home>.
• Perform a system shutdown.
• Switch on the system and wait for the system to boot.

NOTE With the introduction of the Hibernation Mode, system configura-

tion changes are not applied if the system is switched off and then
switched on again using the power buttons on the monitor cart.
To correctly apply the modified data, perform a system shutdown.
Open the <Options> - <End Session> menu and click the “Shut-
down system” button. Immediately thereafter, press the Power off
button on the monitor cart.
The system shuts down and switches off automatically.

• If a change is made to "Block time settings", check this function.

Country-specific adaptation of the maximum tube current 0

NOTE A maximum tube current limit is required - as far as known - only

in Denmark.

• Start service program and log in as described under "Service Login".

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12.06 CS PS SP Medical Solutions
Specific system settings 37

Fig. 15: Main_system

• Click <Main system>.

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Medical Solutions 12.06 CS PS SP
38 Specific system settings

Fig. 16: Main system

• Select ARCADIS Varic and click <Next>.

Fig. 17: Main System_Configuration_Current Limitation

• Click <Current limitation>.
• Make country-specific changes (only Denmark) and click <Save>.
• Click <Home>.
• Perform a system shutdown.

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12.06 CS PS SP Medical Solutions
Specific system settings 39

• Switch on the system and wait for the system to boot.

NOTE With the introduction of the Hibernation Mode, system configura-

tion changes are not applied if the system is switched off and then
switched on again using the power buttons on the monitor cart.
To correctly apply the modified data, perform a system shutdown.
Open the <Options> - <End Session> menu and click the “Shut-
down system” button. Immediately thereafter, press the Power off
button on the monitor cart.
The system shuts down and switches off automatically.

Configuring the network (optional) and remote service 0

• Configure the network according to the Configuration Guide,

SPR2-310.843.01.01.xx.xx and the remote connection according to Installation, Sie-
mens Remote Service, SP00-000.816.02.01.xx.xx.

NOTE With the introduction of the Hibernation Mode, system configura-

tion changes are not applied if the system is switched off and
then switched on again using the power buttons on the monitor
cart.
To correctly apply the modified data, perform a system shutdown.
Open the <Options> - <End Session> menu and click the “Shut-
down system” button. Immediately thereafter, press the Power off
button on the monitor cart.
The system shuts down and switches off automatically.

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Medical Solutions 12.06 CS PS SP
40 Specific system settings

Backup 3.1

NOTE A backup must be created following software installation, every

software update, and every system adjustment.

NOTE After a backup group has been successfully burned to CD, the fol-
lowing message is displayed: "Please insert medium in CD-RW in
order to continue."
Confirm this message with "OK".
This does not require a new CD.

• Select "Backup & Restore" in the “Service Software Home Menu”

• Place the backup CD (located in the monitor cart service compartment) in the CD ROM
drive.

Fig. 18: Backup & Restore_Command

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12.06 CS PS SP Medical Solutions
Specific system settings 41

• Select the <Backup> command.

Fig. 19: Backup & Restore_Command_Backup

• Select the respective drive under “Drives”.
- Save to CD ROM (standard save)

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Medical Solutions 12.06 CS PS SP
42 Specific system settings

Fig. 20: Backup & Restore_Command_Backup_Packages

SW - Settings02
• Select “SW-Settings02” under Packages
• Click <Go> and wait until the message “Ready” appears in the footer.

Fig. 21: Backup & Restore_Command_Backup_SW-Settings02

ASPIA settings

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12.06 CS PS SP Medical Solutions
Specific system settings 43

• Select “ASPIA settings” under Packages.

• Click <Go>
- Wait until the message “Ready” is displayed in the footer
ExamSet
• Select “ExamSet” under Packages.
• Click <Go>
- Wait until the message “Ready” is displayed in the footer
Security-Settings
For systems with an HIPAA configuration
• Select “Security-Settings” under Packages.
• Click <Go>
- Wait until the message “Ready” is displayed in the footer
MainSystem
• Select “MainSystem” under Packages.
• Click <Go>
- Wait until the message “Ready” is displayed in the footer
Exiting the backup
• Close the window via <Home>.
• Remove the backup CD ROM from the CD ROM drive.
• Store the CD ROM with the other system documentation.

NOTE It is not possible to back up the database (patient images)!

Store the patient images in an archive.
Saving to CD ROM as a long-term archive is prohibited.

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Medical Solutions 12.06 CS PS SP
44 Final Work Steps
4-
Paper printer (optional)
4Final Work Steps

NOTE If a paper printer was ordered with the system, all mechanical
work and programming was performed at the factory.
In the case of paper printers delivered after the system, they have
to be installed and started up in accordance with the Installation
and Setting instructions SPR2-310.814.03...

Codonics printer 1660L 0

Perform the following steps according to the "User Manual" of the printer:
• Transport instructions (see preface).
Please note:Unpack the printer and remove the two transport pins. Place the printer in
the cart, connect the power cable and the 25-pin plug to the printer (cables are ready for
use in the printer slot of the cart), and set the power switch to "1".
• Install the print media>(General Start-up / p. 23)

NOTE Keep the transport safety materials. They are required when
replacing or shipping the printer.

Sony printer UP-D72 X 0

Perform the following steps according to the user manual for the printer (CD-ROM):
• Unpack the printer.
• Fill the paper tray with paper (follow instructions on paper package).
• Plug in the USB cable.
• Print a test page after the automatic test.
• Follow the instructions on the CD-ROM from the manufacturer in the event of problems.

Sony Printer UP-970 and UP-990 0

Perform the following steps according to the user manual for the printer (CD-ROM):
• Unpack the printer.
• Fill the paper tray with paper (follow instructions on paper package).
• Plug in the USB cable.
• Print a test page after the automatic test.
• Follow the instructions on the CD-ROM from the manufacturer in the event of problems.

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12.06 CS PS SP Medical Solutions
Final Work Steps 45

Final work steps 4.1

IQ test 0

• Perform IQ test according to instructions SPR2-310.820.01....

¹ Remove the supplied IQ test protocols from the monitor cart service compart-
ment.

Completing protocols 0

• After completing all adjustment work steps and check measurements, the responsible
technician must sign and date the test protocols and country-specific protocols to con-
firm that all values have been correctly determined and recorded.

Protective conductor resistance test 0

Transferring the values from the test protocol to the "protective conductor" proto-
col

NOTE If no covers were opened while installing the system and no addi-
tional components (e.g. options) were installed or modified, the
values recorded in the test protocol 1 can be transferred as the
first measured value.
The protective conductor test need not be performed.
Perform the protective conductor resistance test if the conditions
specified above do not apply.
Refer to the section "Protective conductor resistance test during
start-up (if necessary)".

• Complete the "Protective Conductor Resistance" protocol found in the "Protocol" chap-
ter of this manual.
• If the system test protocol only contains the confirmation of the protective conductor
resistance threshold, enter this value in the "Protective conductor resistance" table, row
"Measurement point 1", column "First measured value" (< 0.18 Ohm). Enter "n.a." in
rows "measurement point 2" through "measurement point 22" of column "First mea-
sured value."
• If the system test protocol specifies the measured protective conductor resistance val-
ues and their measurement points, transfer the values to rows "Measurement point 1"
through "Measurement point 22" of column "First measured value". Mark empty fields
with "n.a." as "not applicable".
• In row "(1) Meas. circuit", column "First measured value", enter the text "VDE0751-1
Image C2".

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Medical Solutions 12.06 CS PS SP
46 Final Work Steps

• If specified in the system test protocol, read off the measuring equipment used at the
factory for the protective conductor test.
¹ Enter this measuring equipment in the "Protective conductor resistance" proto-
col, in the "Measuring device, type:" row.
• If specified in the system test protocol, read off the identification of the measuring
equipment specified in the test protocol.
¹ Enter the ID of the measuring equipment in the "Protective conductor resistance"
protocol, in the "Measuring device, Ser. No.:" row.
• Mark the following rows in the "Protective conductor resistance" protocol with "n.a." as
"not applicable":
¹ Row "Meas. inst. calibrated up to:"
¹ Row "Evaluation:"
• Complete the following rows in the "Protective conductor resistance" protocol:
¹ In the row "Date:" enter the current date.
¹ In the "Name" row, enter your name in block letters.
¹ Sign the protocol in the "Signature" row.
• If you want to complete the protocol with additional remarks, enter them in the
"Remarks" table in the protocol addendum.

Protective conductor resistance test during start-up (if necessary)

NOTE If covers were opened while installing the system and/or addi-
tional components (e.g. options) were installed or modified, the
protective conductor resistance value recorded in system test
protocol 1 is invalid.
The protective conductor resistance test has to be performed
after closing all covers.

NOTE Observe the instructions for the protective conductor resistance

test in the "General Information" chapter of these instructions.

• Perform the protective conductor resistance test.

¹ The protective conductor resistance must not exceed 0.2 ohms at any measuring
point.
• Complete the "First measured value" column of the "Protective conductor resistance"
protocol.
• If you want to complete the protocol with additional remarks, enter them in the
"Remarks" table in the protocol addendum.

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12.06 CS PS SP Medical Solutions
Final Work Steps 47
Tab. 6 Measurement points for the protective conductor resistance measurement

Measuring points
Measurement from the protective conductor connection of the power plug to the:
Base unit, handle attachment screw for I.I. cover
Base unit, one attachment screw at I.I. grid
Base unit, one attachment screw at I.I.
Base unit, one attachment screw at SIREPHOS
Base unit, one screw at cover of horizontal carriage
Base unit, one screw at lifting column cover (rotational brake)
Base unit, one screw at lifting column
Base unit, a lateral screw at brake pedal
Base unit, back cover (electronics box)
Base unit, equipotential bonding connection
Base unit, base plate of electronics box (at unpainted location)
Base unit, one screw at the back of each monitor
Monitor cart, one screw at monitor support
Monitor cart, one screw at the small, top back cover
Monitor cart, one screw at the large, lower back cover
Monitor cart, one screw at back cover of switch-on assembly
Monitor cart, one screw at the front cover
Monitor cart, one screw at the right side cover
Monitor cart, one screw at the left side cover
Monitor cart, one screw at the right handle
Monitor cart, one screw at the left handle

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Medical Solutions 12.06 CS PS SP
48 Final Work Steps

Leakage current measurement 0

Transferring the values from the test protocol to the "device leakage current" proto-
col

NOTE If the programmed line voltage has not been changed from its sta-
tus at delivery, and there have been no changes of parts in the
system's primary circuit, the device leakage current value speci-
fied in the test protocol delivered with the system is valid.
The device leakage current test need not be performed.
The value recorded in the test protocol must be used as the "first
measured value" in the "Device Leakage Current" protocol.
Perform the device leakage current measurement if the conditions
specified above do not apply.
Refer to the section "Device leakage current measurement during
start-up (if necessary)".

• Complete the "Device leakage current" protocol found in the "Protocol" section of this
manual.
• Enter the system serial number on the "Serial Number" row of the "Device leakage cur-
rent" protocol.
• If applicable, enter the customer-specific system ID number in the "Customer-specific
ID Number" row of the "Device leakage current" protocol.
• In test protocol 1, table "Alternative leakage current measurement (DIN VDE 0751)" or
"Device leakage current measurement (DIN VDE 0751-1), read off the higher recorded
value between rows "Leakage current under normal operation and with nominal volt-
age" and "Leakage current with power reversion of polarity and nominal voltage."
¹ Enter the higher value from test protocol 1 in the "Device leakage current" proto-
col, row "Device leakage current (highest measured value) [mA]" and in row
"Device leakage current corrected value [mA]", column "First measured value".
• Read off the line voltage in test protocol 1 under "Revision Level".
¹ Enter the value from test protocol 1 in the "Device leakage current" protocol, row
"Line voltage during measurement [V~]", column "First measured value".
• Read off the production resources entered in test protocol 1, table "Production
resources used".
¹ Enter the production resources from test protocol 1 in the "Device leakage cur-
rent" protocol, row "Measuring device: type", column "First measured value".
• Read off the measuring device ID entered in test protocol 1, table "Production
resources used".
¹ Enter the measuring device ID from test protocol 1 in the "Device leakage cur-
rent" protocol, row "Measuring device, ser. no.", column "First measured value".
• In "Device leakage current" protocol, row "(1) Meas. circuit", column "First measured
value", enter the text "VDE0751-1 Image C5".

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Final Work Steps 49

• Mark the following rows in the "Device leakage current" protocol, column "First mea-
sured value", with "n.a." as "not applicable":
¹ Row "Meas. inst. calibrated up to:"
¹ Row "Evaluation:"
• Complete the following rows in the "Device leakage current" protocol, column "First
measured value":
¹ In the row "Date:" enter the current date.
¹ In the "Name" row, enter your name in block letters.
¹ Sign the protocol in the "Signature" row.
• If you want to complete the protocol with additional remarks, enter them in the
"Remarks" table in the protocol addendum.

Device leakage current measurement during start-up (if necessary)

NOTE If the programmed line voltage has been changed from its status
at delivery, and/or there have been changes of parts in the sys-
tem's primary circuit, the device leakage current value specified
in test protocol 1 delivered with the system is no longer valid.
The device leakage current measurement has to be performed.

NOTE Observe the leakage current measurement instructions in the

"General Information" chapter of these instructions.

WARNING Electrical voltage!

Non-compliance can lead to severe injury and even death.
¹ The system leakage current measurement may be per-
formed on systems of protection class I only after the
protective conductor test has been passed.

• Perform the device leakage current measurement after successfully completing the
protective conductor test.
• Complete the "First measured value" column of the "Device leakage current" protocol.
• If you want to complete the protocol with additional remarks, enter them in the
"Remarks" table in the protocol addendum.

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50 Final Work Steps

Completing the "ARCADIS Varic Installation" protocol 0

The manufacturer of this product requires information and the legislator demands proofs
that a product delivered free of defects from the factory continues to possess the required
and certified quality properties on installation and start-up.
It is therefore absolutely necessary that the installation report with the installation and
start-up data is sent without delay after completion of the work to the address stated on
the installation report.
You will find the report in the system folder.

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12.06 CS PS SP Medical Solutions
Protocols 51
5-
Protective conductor resistance
5Protocols

System: ARCADIS Varic

Material number: 08080017
Serial number: .........................................................................
Customer-specific identification .........................................................................
number:

Tab. 7

Protective conductor resistance

First measured value Repeat measurement values
Meas. point 1:
.....................................
Meas. point 2:
.....................................
Meas. point 3:
.....................................
Meas. point 4:
.....................................
Meas. point 5:
.....................................
Meas. point 6:
.....................................
Meas. point 7:
.....................................
Meas. point 8:
.....................................
Meas. point 9:
.....................................
Meas. point 10:
.....................................
Meas. point 11:
.....................................
Meas. point 12:
.....................................

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Medical Solutions 12.06 CS PS SP
52 Protocols

Protective conductor resistance

First measured value Repeat measurement values
Meas. point 13:
.....................................
Meas. point 14:
.....................................
Meas. point 15:
.....................................
Meas. point 16:
.....................................
Meas. point 17:
.....................................
Meas. point 18:
.....................................
Meas. point 19:
.....................................
Meas. point 20:
.....................................
Meas. point 21:
.....................................
Meas. point 22:
.....................................
(*1) Measuring circuit:
Measuring device type:
Meas. device ser. no.:
Meas. inst. calibrated up to:
Evaluation: n.a.
Date:
Name:
Signature

(*1) Measuring circuit. See (Fig. 22 / p. 53)

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Protocols 53

Measuring circuit 0

Fig. 22: Measuring circuit for measuring the protective conductor resistance for units that are
disconnected from power, in compliance with DIN VDE 0751-1/2001-10, Fig. C2.
Pos. 1 Measurement setup (measuring device)
Pos. 2 System
Pos. 3 Application part (if applicable)

Comments: 0

Tab. 8

Date Comments Name Signature

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Medical Solutions 12.06 CS PS SP
54 Protocols

Date Comments Name Signature

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12.06 CS PS SP Medical Solutions
Protocols 55

System leakage current 5.1

System: ARCADIS Varic

Material number: 08080017
Serial number: .........................................................................
Customer-specific identification .........................................................................
number:

Tab. 9

System leakage current

First measured value Repeat measurement values
System leakage current
(Highest measured value)
[mA]
Line voltage during the mea-
surement
[V~]
System leakage current
corrected value [mA]
(*1) Measuring circuit:
Measuring device type:
Meas. device ser. no.:
Measuring device,
calibrated to:
Evaluation:
Date:
Name:
Signature:

(*1) Measuring circuit: See (Fig. 23 / p. 56) through (Fig. 26 / p. 57)

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Medical Solutions 12.06 CS PS SP
56 Protocols

Measuring circuit 0

Direct measurement

Fig. 23: Measuring circuit for direct measurement of the system leakage current in compliance
with DIN VDE 0751-1/2001-10, Fig. C5 for protection class I.
Pos. 1 = System
Pos. 2 = Application part type B (if available)
Pos. 3 = Measurement setup (integrated into measuring device)

Fig. 24: Measuring circuit for direct measurement of the system leakage current in compliance
with DIN VDE 0751-1/2001-10, Fig. C5 for protection class II.
Pos. 1 = System
Pos. 2 = Application part (if applicable)
Pos. 3 = Measurement setup (integrated into measuring device)

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Protocols 57

Differential measurement

Fig. 25: Measuring circuit for measuring the system leakage current according to the differential
current method in compliance with DIN VDE 0751-1/2001-10, Fig. C6 for protection
class I.
Pos. 1 = System
Pos. 2 = Application part type B (if available)
Pos. 3 = Measurement setup (integrated into measuring device)

Fig. 26: Measuring circuit for measuring the system leakage current according to the differential
current method in compliance with DIN VDE 0751-1/2001-10, Fig. C6 for protection
class II.
Pos. 1 = System
Pos. 2 = Application part (if applicable)
Pos. 3 = Measurement setup (integrated into measuring device)

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Comments: 0

Tab. 10

Date Comments Name Signature

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Protocols 59

C-arm movement and emergency stop 5.2

System: ARCADIS Varic

Material number: 08080017
Serial number: .........................................................................
Customer-specific identification .........................................................................
number:

Tab. 11 C-arm movement and emergency stop protocol

Movement OK Name Date Initials

Yes/No
Releasing/locking the brakes
Downward movement, position
1
Downward movement, position
2
The warning signals sound as
described.
Function,
EMERGENCY_STOP_button

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60 Protocols

Network checklist 5.3

System: ARCADIS Varic

Material number: 08080017
Serial number: .........................................................................
Customer-specific identification .........................................................................
number:

Network checklist (1+) For SAP order no.:_______________________

Will the system have a network connection (HIS/RIS, Camera, Yes No

PACS) ?

Mandatory for image system with network connection!

To ensure that the system is preconfigured at the factory and thus optimize installation at the customer site, we
request that you complete and return this list if a network connection is available (and used).
Person responsible for network configuration at customer site

Name:
Phone / Fax:
E-mail:

System network data

Tab. 12 System network data

Not networked
Identification:
Computer name * Configuration/ Local host/ TCP IP address
IP address:
TCP/ IP address * Configuration/ Local host/ TCP IP address

Subnet mask * Configuration/ Local host/ TCP IP address

Gateways * Configuration/ Local host/ TCP IP address

General: Local AE title for:

HIS/RIS * Configuration/ DICOM/ General
Study transfer * Configuration/ DICOM/ General

Print * Configuration/ DICOM/ General

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Protocols 61

Remarks

Network data for HIS/RIS network partner (only with HIS/RIS option)
Tab. 13 Network data for HIS/RIS

not available
Product: Version: Manufacturer:
Host properties:
Host name * Configuration/ DICOM/ HIS RIS nodes

TCP/ IP address * Configuration/ DICOM/ HIS RIS nodes

General node properties

Logical name * Configuration/ DICOM/ HIS RIS nodes

Application entity
AE title * Configuration/ DICOM/ HIS RIS nodes

Port number * Configuration/ DICOM/ HIS RIS nodes

Remark:

Network checklist (2+)

Network data for reporting console / archive system (only with DICOM Basic option)
(1)
Tab. 14 Network data for reporting console/archiving system

Information on each: Reporting console/ not available

archive system
Product: Version: Manufacturer:
Host properties:
Host name * Configuration/ DICOM/ Network nodes

TCP/ IP address * Configuration/ DICOM/ Network nodes

General node properties:

Logical name * Configuration/ DICOM/ Network nodes

Application entity:
AE title * Configuration/ DICOM/ Network nodes

Port number * Configuration/ DICOM/ Network nodes

Supported DICOM services:

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Storage Yes No * Configuration/ DICOM/ Network nodes

Storage commitment Yes No * Configuration/ DICOM/ Network nodes

Query Node name: * Configuration/ DICOM/ Network nodes

Query Yes * Configuration/ DICOM/ Network nodes

No
Retrieve Yes * Configuration/DICOM/Network nodes
No
Remark:

Network data for reporting console/archive system (only with DICOM Basic option)
(2)
Tab. 15 Network data for reporting console/archiving system

Information on each: Reporting console/ not available

archive system
Product: Version: Manufacturer:
Host properties:
Host name * Configuration/ DICOM/ Network nodes

TCP/ IP address * Configuration/ DICOM/ Network nodes

General node properties:

Logical name * Configuration/ DICOM/ Network nodes

Application entity:
AE title * Configuration/ DICOM/ Network nodes

Port number * Configuration/ DICOM/ Network nodes

Supported DICOM services:

Storage Yes No * Configuration/ DICOM/ Network nodes

Storage commitment Yes No * Configuration/ DICOM/ Network nodes

Query Node name: * Configuration/ DICOM/ Network nodes

Query Yes * Configuration/ DICOM/ Network nodes

No
Retrieve Yes * Configuration/DICOM/Network nodes
No
Remark:

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Network checklist (3-)

Network data for a DICOM camera in the network (only with the DICOM Print option)
(1)
Tab. 16 Network data for DICOM camera in the network

Information for Every camera No camera available

Product: Version: Manufacturer:
Default camera Yes No
Host properties:
Host name * Configuration/ DICOM/ Print devices

TCP/ IP address * Configuration/ DICOM/ Print devices

General node properties:

Logical name * Configuration/ DICOM/ Print devices

Application entity:
AE title * Configuration/ DICOM/ Print devices

Port number * Configuration/DICOM/Print devices

Remark:

Network data for a DICOM camera in the network (only with the DICOM Print option)
(2)
Tab. 17 Network data for DICOM camera in the network

Information for Every camera No camera available

Product: Version: Manufacturer:
Default camera Yes No
Host properties:
Host name * Configuration/ DICOM/ Print devices

TCP/ IP address * Configuration/ DICOM/ Print devices

General node properties:

Logical name * Configuration/ DICOM/ Print devices

Application entity:
AE title * Configuration/ DICOM/ Print devices

Port number * Configuration/DICOM/Print devices

Remark:

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Medical Solutions 12.06 CS PS SP
64 Changes to previous version
6Changes to previous version 6-

Section Changes
Specific system settings The specification for the buzzer setting for the USA was
changed as follows:
Warning time limit: changed from "45" to "50"
Blocking time limit: changed from "5" to "0"

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