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.
English
Doc. Gen. Date: 11.05
2005
Page 2
2Revision / 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 procedures.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 2 of 70
Medical Solutions
Page 3
Table of Contents3
1-0Table of Contents
1 _______ General ________________________________________________________ 6
12 ______ Changes to Previous Version_____________________________________ 69
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 5 of 70
Page 6
6General
1General
2-
Performance of work0
Any technician duly assigned by the local Siemens office is authorized to perform maintenance and service work.
UCertain tasks may also be performed by other technical personnel (e.g. the customer's
hospital technicians). These tasks are marked by this icon.
It is absolutely necessary to
•follow all instructions in textual and graphic form and to
•use the specified tools, test equipment and aids.
You can also contact your national Siemens Uptime Service Center for support.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 6 of 70
Medical Solutions
Page 7
General7
Text labeling0
DANGER
WARNING
CAUTION
NOTICE
DANGER indicates an immediate danger that if disregarded will
cause death or serious physical injury.
¹
WARNING indicates a possible danger that if disregarded can
cause death or serious physical injury.
¹
CAUTION used with the safety alert icon indicates a possible danger that if disregarded will or can lead to minor or moderate physical injury and/or damage to property.
¹
NOTICE used without the safety alert icon indicates a possible
danger that if disregarded can or will lead to an undesirable outcome or state other than death, physical injury or property damage.
¹
NOTE
NOTE is used to indicate information that explains the proper way
to use devices or to carry out a process, i.e., provides pointers and
tips.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 7 of 70
Page 8
8General
Icons0
XWarning about ionizing radiation or radioactive substances. Tests and adjustments that
must be performed with the radiation switched on are indicated by this radiation warning
icon.
.
VDangerous electrical voltage > 25 VAC or > 60 VDC.
CCaution! General hazard warning.
EESD: Warning about electrostatically sensitive components.
PReport icon. Used to indicate entries in certificates.
UCertain tasks can also be performed by other technical personnel (e.g. the customer's
hospital technicians).
Fig. 1:
Certain sections apply only to the USA. These sections are marked with this icon.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 8 of 70
Medical Solutions
Page 9
General9
Information on product safety and protective measures0
DANGER
DANGER
While performing maintenance and service work
on the MOBILETT XP Digital with the covers removed,
it is possible to come into contact with components under voltage.
Carelessness can result in death or serious bodily injury.
When conducting maintenance and service work, follow:
¹ the product-specific safety information contained in the
technical documentation,
¹ and the general safety information (TD00-000.860.01...).
Remove or install components only if:
¹ - The system is switched off, and
¹ - The capacitors are discharged, and
¹ - The ESD guidelines are followed, and
¹ - The batteries have been disconnected.
DANGER
Releasing radiation:
¹ Checks and settings for which radiation must be
released are marked with the radiation warning symbol.
¹ Radiation protection measures must be used.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 9 of 70
Page 10
10General
DANGER
To avoid electrical shock from components under voltage, also be
aware that:
The capacitors of the capacitor bank can be electrically charged
even when the system is switched off and the power cable is disconnected!
Individual capacitors of the capacitor bank may have been disconnected from the discharging circuit, erroneously or as a result of
failure, and can still be electrically charged!
Disconnect the battery blocks in the XP Digital prior to maintenance and service work!
Carelessness can result in death or serious bodily injury.
¹ Make sure that no parts or tools fall into the unit;
¹ Do not touch potentially dangerous
components(Fig.2/p.11)
¹ If loose parts must be removed from the unit, use only
insulated tools;
¹ Protect the work area so that no other persons are able
touch the unit while the covers are open or removed!
•Switch the unit off before servicing or maintenance. Always disconnect the power plug
first.
•Make sure that the main switch is switched off.
•The capacitor bank discharges to < 40 V in approx. 15 minutes.
¹ The safety covers can be removed after this period has elapsed.
•Prior to performing any work, it must be verified that areas with dangerous voltage are
voltage-free (Fig.2/p.11).
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 10 of 70
Medical Solutions
Page 11
General11
Fig. 2:Locations with dangerous voltage
VWith housing covers open and safety covers removed.
Back:
Left side:
Right side:
CAUTION: DC voltage (300 V) from the battery block to PCB D982!
Always disconnect the battery plug from BK1-BK4.
CAUTION: DC voltage (440V) at capacitor bank (D927)
CAUTION: DC voltage (440V) directly at the capacitor bank!
CAUTION: DC voltage (440V) directly at the capacitor bank!
CAUTION: AC voltage (> 100 V or > 60 V - half line voltage) at power supplies U1 and U2 when the power cord is connected.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 11 of 70
Page 12
12General
System overview - user0
Fig. 3:User overview
(1) Hanger for lead apron(13) Castors
(2) Articulated arm(14) Console with chassis
(3) Sensor for IR remote control (optional)(15) IR remote control (optional)
(4) DAP display (optional)(16) Holder for IR remote control (optional)
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 12 of 70
Medical Solutions
Page 13
General13
Orientation0
Fig. 4:Top view of system_01
System orientation to clarify the technical description
AbbreviationsExplanation
UvUser view - back (User view)
LLeft side of unit (left)
RRight side of unit (right)
FFront (front)
fwFront wheels (front wheels)
saSupport arm (support arm)
TTube (single tank)
CMultileaf collimator (collimator)
ddDAP display (dose display)
NOTE
These orientation indicators are used in all technical documents.
Descriptions are always from the “forward travel” user view. Always use this perspective when communicating with third parties
(e.g., USC/HSC).
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 13 of 70
Page 14
14General
System overview - service0
Fig. 5:Schematic overview of XP Digital
MOBILETT XP Digital parts
AbbreviationsExplanation
D916/D919CPU board/X-ray interface
D917Galvanic separation for S27/DAP/remote
RcbRemote control board (remote control option)
SW1Key switch, power ON/OFF
Z1Line filter
C1 (R1)Capacitor for inverter with discharge resistor (front left side / not
shown here)
C2 (R2)Starter capacitor with discharge resistor
R3-R5, R6 (X9)Discharge resistor capacitor bank (front right side)
Capacitor bank12 x 10 mF capacitors, mounted on D972
K22Main relay
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 14 of 70
Medical Solutions
Page 15
General15
D909X-ray display and keyboard
U1+5V / ± 15V power supply
U2+24V power supply
D927Power supply
D952Charging board capacitor bank (behind D927)
D962kV inverter (behind D927)
D972Capacitor bank board (behind D927)
SaSupport arm adjusting spring
lw/rw/swSupport wheels and back wheels
D982Battery charger
D102Motor drive control
BK1 / BK2Battery block, left
BK3 / BK4Battery block, right
mr/mlMotor right / motor left
CXDI PCLaptop for the imaging system
CXDI DetectorCXDI flat detector
Power boxConnecting unit between CXDI PC and CXDI detector
U3DC converter 300V DC/24V DC
U4 Inverter 24V DC/220V AC
U5Power supply CXDI PC (laptop)
Optional parts for MOBILETT XP Digital (not shown in illustration)
DAP chamberDose area product measuring chamber
D991DAP adapter card (inside the collimator cover)
DAP displayDAP display board (in the lower arm segment cover)
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 15 of 70
Page 16
16General
Cleaning0
•Always disconnect the MOBILETT from the power supply and switch it off before clean-
ing or disinfecting it.
•Never use abrasive cleaners or cleaning agents with solvents (e.g. cleaning solutions,
alcohol or spot removers), since they may damage housing surfaces.
•Do not spray anything on or into the unit.
•Wipe off the MOBILETT with a cloth moistened in water or a diluted, lukewarm solution
of water and dishwashing liquid.
For more information, see the chapter on "Cleaning and disinfection” in the operating
instructions.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 16 of 70
Medical Solutions
Page 17
General start-up information17
2General start-up inform ation
3-
Required documents0
PCheck the documents delivered for completeness.
Ring binders containing user documents:
•Operator ManualSPR8-230.621.30..
Ring binders containing technical documents:
•General Safety InformationTD00-000.860.01...
•Installation and Start-upSPR8-230.814.30...
•Software InstallationSPR8-230.816.30...
•Quality AssuranceSPR8-230.820.30...
•Maintenance ProtocolSPR8-230.832.01...
•Wiring DiagramSPR8-230.844.30...
•Disposal InstructionsSPR8-230.861.30...
•Manufacturer's certificatesn.a.
The MOBILETT XP Digital password list can be obtained by accessing the “Knowledgebase” or from the Troubleshooting Guide SPR8-230.840.30...
•MOBILETT XP Digital password listn.a.
The following additional documents are required to configure DICOM Hardcopy:
•General Hardcopy Camera InformationSPR8-230.814.40..
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
•Storage oscilloscope (± 2.5 % accuracy) or kV meter.
•Storage oscilloscope (±2.5 % accuracy) or mAs meter.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 18 of 70
Medical Solutions
Page 19
General start-up information19
Start-up information0
•The start-up procedure described here corresponds to a functional test. All adjust-
ments and calibrations are performed at the factory. The MOBILETT XP Digital is ready
for operation on completion of the start-up report.
•The top cover has to be removed to access the CXDI PC or perform measurements on
D916. Place the top cover on a table or similar surface. All cables remain connected.
•The unit can be connected to line voltages of 100-130 V ( ± 10%) or 200-240 V ( ±
10%). The unit automatically adjusts to the existing line voltage.
NOTE
Observe the nominal current of the fuses for the on-site power
connections:
- 15A slow-blow (on-site) for 100-130V ± 10% or
- 15A slow-blow (on-site) for 200-240 V ± 10% line voltage.
The power cable for this device is equipped with a standard safety
plug.
Attach a power plug that is compliant with local standards if necessary.
•Following start-up, country-specific tests must be performed if necessary.
For example:
Acceptance test according to §16 of the X-ray Ordinance (Germany):
Use the measurements in the test certificate provided as the initial values for the required
measurements.
The following values were measured by the manufacturer; refer to the test certificate:
- Brightness of the light localizer
- Filter values (Al equivalent for tube assembly and collimator)
- Coincidence of light field and radiation field
- Accuracy of the tube voltage
- Accuracy of the kV value steps
- Accuracy of the mAs values
- Reproducibility of dose values
•The test/measured values marked by the report icon must be entered in the start-up re-
port located at the end of this manual.
NOTE
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
Recording information immediately during start-up saves time.
Fill in the report form after completing each task.
The start-up report is a component of this documentation.
Page 19 of 70
11.05CS SD 24
Page 20
20General start-up information
Information on the protective conductor resistance test0
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.
Initial measurement
Perform the protective conductor test after completion of all work.
The measurement must be performed according to DIN VDE 0751, Part 1 (see 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 components of the system are
not mistaken for protective conductor connections.
During the measurement, move the power cable and additional connection cables with an
integrated protective conductor section by section to detect cable breaks.
The protective conductor resistance must not exceed 0.2 Ohms.
The values must be recorded as initial measurements, and the measuring points noted, in
the protective conductor resistance report.
The measuring procedure and the measuring device used (designation and serial number) must also be documented.
Fig. 6: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= System
Pos. 2= Application part type B (if available)
Pos. 3= Measurement setup (integrated into measuring device)
Repeat measurement
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 20 of 70
Medical Solutions
Page 21
General start-up information21
In the case of maintenance or repairs, perform the protective conductor resistance measurement again.
Document and assess the values determined in the repeat measurement.
The measurement must be performed according to DIN VDE 0751, Part 1 (see 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 components of the system are
not mistaken for protective conductor connections.
During the measurement, move the power cable and additional connection cables with an
integrated protective conductor section by section to detect cable breaks.
The protective conductor resistance must not exceed 0.2 Ohms.
The values determined in the repeat measurement must be recorded and assessed, and
the measuring points noted, in the protective conductor resistance report.
The measuring procedure and the measuring device used (designation and serial number) must also be documented.
NOTE
For evaluation purposes, the first measured value and the values
documented during 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 protective conductor connections (protective conductor or contacts) - even if the
limit value of 0.2 ohms is not exceeded.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 21 of 70
Page 22
22General start-up information
Information on measuring the leakage current0
Observe the instructions in the "Safety Rules for Installation and Repair"
(ARTD-002.731.17 ...).
WARNING
Electrical voltage!
Non-compliance can lead to severe injury and even death.
¹ The leakage current measurement may be performed on
systems of protection class I only after the protective
conductor test has been passed.
Initial measurement
Perform the leakage current measurement after completion of all work.
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 leakage current according to the differential current method (measurement setup according to (Fig.7/p.22)) 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 leakage current measuring device
and any additional manufacturer information restricting the use of the measuring device.
Fig. 7: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)
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 22 of 70
Medical Solutions
Page 23
General start-up information23
If the direct measurement of the leakage current is used (measurement setup according
to (Fig.8/p.23)), the system must be insulated during the measurement and must not be
touched.
Fig. 8:Measuring circuit for direct measurement of the system leakage current in compliance
Pos. 1= System
Pos. 2= Application part type B (if available)
Pos. 3= Measurement setup (integrated into measuring device)
with DIN VDE 0751-1/2001-10, Fig. C5 for protection class I.
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 leakage current (measurement setup according to (Fig.8/p.23)).
¹ Third-person access to the system must be prevented.
The system must be switched on during measurement. Measuring devices with automated measuring sequences must therefore be set to manual measurement.
Enter the highest value as the first measured value in the leakage current report.
This value must not exceed the permissible leakage current values according to DIN VDE
0751-1/2001-10, Table F.1, line "leakage current for devices 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 measurement 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).
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 23 of 70
Page 24
24General start-up information
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 leakage current measurement must be repeated.
The same measuring conditions as in the first measurement apply.
Record and assess the highest value determined in the repeat measurement in the existing system leakage current report.
This value must not exceed the permissible leakage current values according to DIN VDE
0751-1/2001-10, Table F.1, line "leakage current for devices 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 measurement 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).
NOTE
For evaluation purposes, the first measured value and the values
documented during 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 (damaged insulation, damage
from moisture, defective interference suppressor, etc.) - even if the
limit value of 2.5 mA is not exceeded.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 24 of 70
Medical Solutions
Page 25
General start-up information25
Information on measuring the patient leakage current0
Observe the instructions in the "Safety Rules for Installation and Repair"
(ARTD-002.731.17 ...).
The patient leakage current must be measured at each application part for systems of
protection class I with type B application parts.)
If the application part has a surface made of non-conductive material, a conductive material (e.g., aluminum foil) must be placed on the surface. The conductive surface must be
large enough to approximate the contact surface of the patient with the application part.
In the case of a flat detector, completely cover the contact surface with aluminum foil.
During the measurement, hold the aluminum foil securely to the application part to be
measured using approx. 0.5 N/cm
2
of pressure.
WARNING
Initial measurement
The patient leakage current must be measured for each application part.
The measurement must be made according to DIN VDE 0751, Part 1 (see
ARTD-002.731.17...).
Electrical voltage!
Non-compliance can lead to severe injury and even death.
¹ The patient leakage current measurement may be per-
formed on systems of protection class I only after the
protective conductor test has been passed.
Fig. 9:Measuring circuit for measurement of the patient leakage current in a type B application
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 25 of 70
Page 26
26General start-up information
part with a protective conductor in compliance with DIN VDE 0751-1/2001-10, Fig. C10.
Pos. 1= System
Pos. 2= Application part type B
Pos. 3= Measurement setup (integrated into measuring device)
The system must be switched on during measurement. Measuring devices with automated measuring sequences must therefore be set to manual measurement.
The determined values, including the application parts/measuring points, must be entered
as the first measured values in the patient leakage current report.
The values for each application part may not exceed the permissible leakage current values according to DIN VDE 0751-1/ 2001-10, table F.1, line "patient leakage current" of
0.01 mA for direct current and 0.1 mA for alternating current.
Document the measuring procedure and the measuring device used (designation and
serial number).
Repeat measurement
When maintenance or repair work capable of affecting the patient leakage current is performed on the system (e.g. repairs to the protective conductor connections, replacement
of parts in the primary power supply circuit, replacement of application parts, technical
changes to application parts), the patient leakage current must be remeasured and documented for each application part.
The same measuring conditions as in the first measurement apply.
The values determined in the repeat measurement, including the application parts/measuring points, must be recorded and assessed in the patient leakage current report.
The values may not exceed the permissible leakage current values according to DIN VDE
0751-1/ 2001-10, table F.1, line "patient leakage current" of 0.01 mA for direct current and
0.1 mA for alternating current.
Document the measuring procedure and the measuring device used (designation and
serial number).
NOTE
For evaluation purposes, the first measured value and the values
documented during 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 system (protective conductor connection damage, insulation damage, damage from moisture, etc.) - even if the limit value of 0.01 mA for
direct current and 0.1 mA for alternating current is not exceeded.
.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 26 of 70
Medical Solutions
Page 27
Unpacking and visual inspection27
3Unpacking and visual in spection
4-
Unpacking0
Fig. 10: Unpacking
•Please follow the unpacking instructions.
•Check the manual movement mode and the hand brake.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 27 of 70
Page 28
28Unpacking and visual inspection
Visual inspection0
P•Check the unit for external damage (cracks, breaks, scratches, corrosion etc.).
•Check whether the single tank or the multileaf collimator show any signs of mechanical
defects which might impair the radiation protection.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 28 of 70
Medical Solutions
Page 29
Unpacking and visual inspection29
Mechanical function test0
Cable winch0
P•Pull out the cable until it is completely unwound.
•Hold the cable with one hand near the duct to slow it down as it is being wound. Pull up
the brake of the cable winch and wind up the cable completely.
This device is equipped with a standard safety plug. Attach a power plug that is compliant
with local standards if necessary.
Support arm movements0
P•Unlock the support arm. Then check its movements, including several stops. If the DAP
chamber option is included in the delivery, it must be attached to the collimator. The arm
should be easy to move through its full range using one hand and should stop in every
position without any additional movement (up or down).
Fig. 11: Positioning of support arm
Single tank and collimator movements0
P•Turn the collimator with the handle to the end positions ±90°.
•Rotate the tube to all of its commonly used working and park positions.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 29 of 70
Page 30
30Checking the shock sensors
4Checking the shock sensors
5-
Checking the shock sensors0
PPrior to startup, the 4 shock sensors must be checked.
Fig. 12: Shock sensor
If a shock sensor has been activated (colored red), the CXDI detector has to be replaced
before start-up.
•Check the shock sensors.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 30 of 70
Medical Solutions
Page 31
Start-up31
5Start-up
6-
Line voltage0
PThe power supply range can vary between 100V AC and 240V AC. Use the DVM to check
the voltage at the socket.
NOTE
The system automatically adjusts to the local line voltage.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 31 of 70
Page 32
32Start-up
Controls and displays0
Battery charging operation0
PThe MOBILETT XP Digital is switched off.
Connect the power plug and check whether the AC symbol (~) lights up on the control
panel (4/Fig. 13 / p. 32).
The battery charge status displays must light up. (The batteries are charging)
Exposure operation0
NOTE
NOTE
At least one of the 3 battery status LEDs must light up for the
checks in exposure operation (3/Fig. 13 / p. 32).
Otherwise, charge the batteries until this operating state is
reached (min. charging time: 2 hrs.).
If the unit has not been used for some time, error ERR13 may appear, indicating a high leakage current at the capacitor bank.
Switch the system off and back on to correct this problem.
If the error persists even after the system has been switched off
and on several times, execute Service Program 1, "Format Capacitor Bank," according to the system troubleshooting instructions.
Fig. 13: Battery status display
•Disconnect the main power cord from the power supply and wind it completely around
the cable spool.
•Switch the unit on. Wait for the initialization process to finish (acoustic signal, KV/mAs
displays visible).
•Check the battery status.
•Switch to manual/analog operation (A/D button on control panel).
•Use the "± kV/± mAs" keys to select different values for KV and mAs.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 32 of 70
Medical Solutions
Page 33
Start-up33
P•Check the following functions according to the operator manual:
- Motor drive
- Locking brake
Fig. 14: XP Digital functional check
(1) Power key switch ON/OFF/charge battery
(2) Hand brake
(3) Main power cord
(4) Motor drive - forward/reverse
(5) Brake/release for cable winch
Lead apron holder0
PAttach the supplied lead apron holder to the support arm joint as needed.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 33 of 70
Page 34
34Start-up
Fig. 15: Holder
Collimator function0
P•Completely open the collimator.
•Check the functioning of the light keys on the collimator.
•Check the manual collimations with the light on.
•The light switches off after approx. 20 sec.
•Test the collimator light key on the control panel (1/Fig. 13 / p. 32).
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 34 of 70
Medical Solutions
Page 35
Start-up35
Calibrating the CXDI detector0
Start-up of the MOBILETT XP Digital requires a one-time calibration of the CXDI detector.
Four test exposures are performed during this procedure.
Preparation
•Remove the grid (if available).
•Switch the MOBILETT XP Digital on and start the CXDI PC (digital operation)
•Center the CXDI detector with respect to the tube assembly (SID 150 cm).
•Set to maximum collimation
Procedure
Perform the following steps from the user application:
•Select SYSTEM/CALIBRATION.
•Enter the following parameters in the list boxes:
¹ If error messages ("Too much/little dose", "Collimator is used") are displayed
during calibration, the KV and mAs values have to be adjusted accordingly.
NOTE
If the calibration is unsuccessful, check the calibration settings.
The KV and mAs settings may have to be adjusted.
If the calibration continues to be unsuccessful, start the detector
self-test (see Troubleshooting Guide SPR8-230.240.30...) or notify
the Uptime Support Center.
•Check the detector centering. No other objects affecting the calibration may be located
in the beam path.
•Click "START" to begin the calibration.
•Follow the on-screen instructions.
¹ Four exposures are required. No error messages should be displayed. The cali-
bration completion is indicated.
•Use “EXIT” to exit the menu.
•Switch the MOBILETT XP Digital "OFF" and back "ON".
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 35 of 70
Page 36
36Start-up
Exposure release with high voltage0
NOTE
P
If the “DAP” and/or “Remote Control” options are installed, they
can be tested for proper function during the following tests involving release of X-ray radiation.
Checking the preparation limit time0
•Select manual/analog operation on the MOBILETT XP Digital control panel (A/D but-
ton).
•Close the collimator and set 60 kV/10 mAs on the control panel.
•The control display for "exposure circuit ready" on the control panel must light up green.
•Set the exposure switch (S27) to preparation and check the "exposure ready" acoustic
signal.
•Hold 'Preparation' and check the preparation limit time of approx. 20 seconds. ERR 25
appears on the display (preparation time without exposure).
•Acknowledge the error with the "collimator light" key on the control panel.
Release an exposure0
X•Release an exposure.
¹ The radiation indicator on the control panel lights up during the exposure; at the
same time an acoustic signal sounds and the "exposure circuit ready" light on
the control panel goes out.
•"Exposure circuit ready" on the control panel lights up within 15 sec maximum.
Manual exposure termination0
The user must be able to cancel an exposure at any time.
•Set a midrange kV value (e.g., 70 kV) and the highest possible mAs value.
X
•Release an exposure and interrupt it immediately. "ERR 39" appears on the display and
a succession of brief signal tones (exposure cancelled) sounds. Acknowledge the error
message with the "collimator light" key on the control panel.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 36 of 70
Medical Solutions
Page 37
Start-up37
Light field/radiation field0
Checking the light and radiation field
•Place the detector (35 cm x 43 cm) on the tabletop.
•Set the central beam so it is vertical.
•Set a vertical SID of 100 cm; measure to the upper edge of the detector using the tape
measure in the collimator.
•Switch on the light localizer and set a light field of approx. 30 cm x 30 cm.
•Place the lead ruler (centering cross) centered on the detector.
•Measure the light field and make a note of the dimensions (Fig. 16 / p. 37).
•Position a washer as a side marker.
Fig. 16: Centering cross
•Create a test patient.
•Select an organ program from the "test" range, with approx. 60 kV, 4 mAs.
X
•Release an exposure.
Evaluation: light field to radiation field0
•Using the centering cross, evaluate on screen, on all four sides, the deviations (A, C
and B, D) between the recorded light field and the radiation field edges (Fig. 17 / p. 38).
Use the zoom function as necessary.
P¹ The maximum total allowable deviation from the SID is 1.7% (regardless of the
prefix). If the deviation is > 1.7%, the collimator must be adjusted (see the
"Replacement of Parts" instructions).
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 37 of 70
Page 38
38Start-up
Fig. 17: Light field/radiation film
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 38 of 70
Medical Solutions
Page 39
Start-up39
Configuration of the imaging system0
PConfigure the MOBILETT XP Digital for user setting and network connection according to
the “Software Configuration” chapter of "Software Installation” SPR8-230.816.30....
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 39 of 70
Page 40
40Start-up
Checking the image quality0
P At start-up, the touch screen display must be checked with the SMPTE test image (bright-
ness and contrast) and the image quality parameters recorded using the quality assur-
ance document SPR8-230.820.30....
File the filled-out quality assurance document in register 9, "Certificates," in the system
binder.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 40 of 70
Medical Solutions
Page 41
Start-up41
Options0
DAP0
PMeasuring device for dose area product (Dose Area Product).
The DAP measuring device is used to measure the kerma area product (kerma = kinetic
energy released in matter) during an X-ray examination. It is primarily used to record the
radiation dose a patient is exposed to.
The DAP is calibrated at the factory:
•Press the test button on the DAP display, a value between 80-120 µGym
2
tion 0.1 µGym
tion 0.01 µGym
If the display is incorrect, the measuring device must be calibrated. See the
"Replacement of Parts" instructions, SPR8-230.841.30...).
) or in the case of a high-resolution chamber, 8-12 µGym2 (DAP resolu-
2
) must be subsequently displayed.
2
(DAP resolu-
X
•Check the function of the DAP display by releasing an exposure. The DAP display
shows a measurement value depending on the object in the beam path.
Remote control0
P•Adhere the remote control holder to the front right or left side (16/15/Fig. 3 / p. 12).
•Switch on the MOBILETT XP Digital.
X
•Check the "collimator light" and "exposure release" functions of the remote control.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 41 of 70
Page 42
42DHHS
6DHHS
7-
DHHS tests (USA only)0
The following tests must be performed and recorded to satisfy the DHHS requirements:
•kV accuracy
•mAs accuracy
•Reproducibility
NOTE
All of the following DHHS checks are performed in manual operation!
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 42 of 70
Medical Solutions
Page 43
DHHS43
Test of kV accuracy0
Requirement:
The measured kV values must comply with the limit values specified in the tables. One of
two measuring methods can be used:
1. kV meter procedure:
- kV meter based on the filter comparison technique (e.g. PTW-Nomex). Use the correction factor given in the kV meter operating instructions for non-invasive kV measurements.
2. Oscilloscope method:
- Storage oscilloscope with a measuring accuracy of ± 2.5%
kV meter method:0
NOTE
The inherent filtration (Al equivalent) of MOBILETT XP Digital is
3.1mm Al (single tank plus collimator).
An installed DAP measurement chamber increases the inherent filtration by 0.4 mm AL.
•Switch the MOBILETT XP Digital on.
•Maintain or switch to manual operation of the MOBILETT XP.
•Prepare the kV meter for the measurement according to the operating instructions.
•Place the measuring detector on a suitable surface and adjust the single tank to the de-
tector using the light localizer (Fig. 18 / p. 44).
•Set the source-to-image distance to the value specified in the kV meter operating in-
structions.
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 43 of 70
Page 44
44DHHS
Fig. 18: kV measurement
X•Set the following exposure parameters and release an exposure after each setting:
kV meter
Selection
DC voltage
* The measuring inaccuracy of the measuring instrument used must be subtracted from
the specified limit values.
PRecord the measured values.
Exposure parametersLimit values*
52 kV50 mAs49.0 - 55.0 kV
81 kV20 mAs77.0 - 85.0 kV
133 kV12.5 mAs126.4 - 139.6 kV
Oscilloscope method: 0
"KVS" measuring point for the nominal value and “KV” measuring point for the actual
value. The measuring ratio is 30 kV/V.
•Remove the top cover and place on a table or similar surface. All cables remain con-
nected. Measuring points on CPU D916 (see troubleshooting instructions).
•Connect the oscilloscope to the measuring points of the CPU D916 TP KV, KVS, and
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 49 of 70
Page 50
50DHHS
Fig. 24:
Fig. 25:
Step 4)
P
•Calculation of coefficient:
Fig. 26:
In this example, the generator complies with the specification:
C = 0.0105, which is ≤ 0.0450.
•Perform the described procedure and record the results in the DHHS report.
•Complete the DHHS report.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 50 of 70
Medical Solutions
Page 51
Backup51
7Backup
8-
Backup procedure0
Included with delivery of the MOBILETT XP Digital is a backup of the entire C: driveand D:
drive on the system DVD (factory settings).
PFollowing start-up of the MOBILETT XP Digital at the customer site and completion of all
adjustment and configuration steps, a second backup operation of the hard drives to CD
is performed.
A "Backup of Configuration" is also created. The "Backup of Configuration" includes all
configuration settings, organ programs, log files, and images from the external storage.
This ensures that the customer configuration can be restored or that the imaging system
can be reinstalled with the customer configuration.
Backup of hard disks0
Prerequisite
The Mobilett XP Digital has been completely installed and configured according to customer specifications. All checks have been successfully completed.
The MOBILETT XP Digital System DVD is available.
At least 2 blank writable CDs are available (2 blank CDs are included with the delivery).
Delete all test exposures in “local Temp Storage” and in “External Storage” prior to the
backup.
Procedure
•The MOBILETT XP Digital is switched off.
•Open the top cover of the MOBILETT XP Digital and place on a table or similar surface.
All cables remain connected (access to CXDI PC).
•Open the CXDI PC (laptop) to access the keyboard and display. Do NOT switch on the
CXDI PC if it is disconnected from the MOBILETT XP Digital. Otherwise, the display
setting can switch to the default setting without touch screen display on the laptop.
•Label the blank CDs used for the backup with the date and image and number them se-
quentially (min. 2 CDRs required)
•Switch the MOBILETT XP Digital "ON" and place the system DVD in the DVD/RW drive
of the CXDI PC (boot from the system DVD)
NOTE
If necessary, set the boot device to DVD-ROM in the laptop's BIOS.
Access to BIOS: while system is booting, press the F2 key and enter the administrator password "99999".
¹ The display shows the following menu:
- 1 - Backup the complete hard drive (c: + d:)
- 2 - Restore the complete hard drive (c: + d:)
- 3 - Restore factory settings (c: + d:)
- 4 - Back up the complete hard drive (c:)
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 51 of 70
Page 52
52Backup
- 5 - Restore the complete hard drive (c:)
- 6 - Use GHOST interactive
-E - Exit
•Select "1" - Back up the complete hard drive (c: + d:)
¹ Follow the on-screen instructions
¹ The backup completion is displayed
•Remove the CD from the DVD/CD RW drive of the CXDI PC.
•Restart the MOBILETT XP Digital and perform the "Backup of Configuration" as de-
scribed below.
Backup of Configuration0
The "Backup of Configuration" includes all configuration settings, organ programs, log
files, and images from the external storage and has to be performed following start-up of
the MOBILETT XP Digital at the customer site.
The imaging system service tool is used to back up all relevant data to the D:\_Siemens_
folder. This folder is written to CD using Windows XP Explorer and stored as a backup
CD.
Prerequisites
The system is completely installed and configured according to customer specifications.
All checks have been successfully completed.
At least one blank writable CD is available.
Before backup, delete all test exposures from "external storage."
The CXDI PC is accessible (see “Backup of hard disks” earlier).
The MOBILETT XP Digital is switched on and the application has been launched properly.
Procedure
Perform the following steps from the application:
•Select SYSTEM/ CONFIGURATION/ ADMINISTRATOR SETUP/ SERVICE TOOL.
•Enter the administrator password and confirm with “OK”.
¹ See password list.
•Select “Copy files to _Siemens_” from the SERVICE TOOL menu.
•Select “START”.
¹ Enter the service password (see password list)
•Confirm with “OK”.
¹ All necessary files are copied to the "_Siemens_" directory. Existing data is over-
written.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 52 of 70
Medical Solutions
Page 53
Backup53
Writing backup data to CD
After backing up all relevant data to the D:\_Siemens_ folder using the imaging system
service tool, the data in this folder has to be written to CD using Windows XP Explorer.
•Label the blank CD for the backup with the date and "Backup of Configuration" and
number it.
•Select “Explorer” from the SERVICE TOOL menu.
•Start via "START"
¹ Enter the service password (see password list)
•Insert the labeled CD into then CD RW drive of the CXDI PC.
•Copy the “D:\_Siemens_” folder to drive E:\ (CD RW drive).
•Right-click in the right pane of the E:\ drive Explorer window and select "Write these
files to CD".
•Follow the prompts.
¹ The data is saved to CD
•Wait until the write operation is completed.
•Close Explorer.
•Click “Exit” to exit the “SERVICE TOOL”.
•Click “OK” to exit “ADMINISTRATOR SETUP”.
•Switch the MOBILETT XP Digital OFF.
•Close the CXDI PC, secure the CXDI PC transport fastener, and attach the top cover
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 53 of 70
Page 54
54Remaining work
8Remaining work
9-
Final activities0
Protective conductor test0
Observe the protective conductor resistance test information in these instructions.
•Perform the protective conductor test with all covers closed in accordance with
ARTD-002.731.17... The protective conductor resistance must not exceed 0.2 Ohms.
P
P
•The values determined must be recorded as initial measurements in the protective con-
ductor resistance report (chapter 11 of these instructions), and the measuring points
must be given.
•The measuring procedure and the measuring device used (designation and serial num-
ber) must also be documented.
Leakage current measurement0
Observe the leakage current measurement information in these instructions.
•The leakage current must be measured with all covers closed, in accordance with
ARTD-002.731.17... The limit value of 2.5 mA must not be exceeded.
WARNING
•The system must be switched on during measurement. Measuring devices with auto-
mated measuring sequences must therefore be set to manual measurement.
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 leakage current .
¹ Third-person access to the system must be prevented.
P
•Enter the highest value as the first measured value in the leakage current report (chap-
ter 11 of these instructions).
•This value must not exceed the permissible leakage current values according to DIN
VDE 0751-1/2001-10, Table F.1, line "leakage current for devices according to remarks 1 and 3", of 2.5 mA.
P
P
•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 measurement at the nominal value of the line voltage. This must also be documented.
•The measuring procedure (differential measurement or direct measurement) and the
measuring instrument used (designation and serial number) must also be documented.
Patient leakage current measurement0
Observe the patient leakage current measurement information in these instructions.
•The patient leakage current must be measured with all covers closed, in accordance
with ARTD-002.731.17...
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 54 of 70
Medical Solutions
Page 55
Remaining work55
•The patient leakage current must be measured at the flat detector.
•The system must be switched on during measurement. Measuring devices with auto-
mated measuring sequences must therefore be set to manual measurement.
P
•Enter the value determined as the first measured value in the patient leakage current
report (chapter 11 of these instructions).
•This value may not exceed the permissible leakage current values according to DIN
VDE 0751-1/ 2001-10, table F.1, line "patient leakage current" of 0.01 mA for direct current and 0.1 mA for alternating current.
P
•The measuring procedure and the measuring device used (designation and serial num-
ber) must also be documented.
Labels0
Country-specific labeling
P
•The "Warning!" label "This X-ray unit may be dangerous...” is supplied in a number of
languages. Select the correct language and attach the label according to the MOBILETT XP Digital operator manual.
•The "Danger!” label “Explosion hazard...” is supplied in a number of languages. Select
the correct language and attach the label according to the MOBILETT XP Digital operator manual.
•Affix the "Do not open doors to rooms with the unit" label as shown in (Fig. 27 / p. 55).
•For Germany only:
Select the 1.5 m, 2.5 m or 3.5 m "control area" label as required by the customer and
affix it to the bottom of the arm as shown in (Fig. 28 / p. 56).
Fig. 27: "Rambo" label
Siemens AGSPR8-230.814.30.03.02MOBILETT XP Digital
Medical Solutions
11.05CS SD 24
Page 55 of 70
Page 56
56Remaining work
Fig. 28: "Control area" label
Reports0
•Separate the completed 'Start-up report' (chapter 9 of these instructions) from these in-
structions and file it in the system binder, Register 9, "Certificates."
•Separate the completed DHHS report (chapter 10 of these instructions) from
these instructions and file it in the system binder, Register 9, "Certificates."
•Separate the completed protective conductor resistance report, leakage current report,
and patient leakage current report (chapter 11 of these instructions) from these instructions and file them in the system binder, Register 9, "Certificates."
•Complete the "Installation Protocol" included with the unit and send it (by fax) to the ad-
dress listed in the protocol.
MOBILETT XP DigitalSPR8-230.814.30.03.02Siemens AG
11.05CS SD 24
Page 56 of 70
Medical Solutions
Page 57
Start-up report57
9Start-up report
10-
MOBILETT XP Digital0
This protocol confirms operability according to the datasheet. The original document
remains with the unit, and a copy is filed at the local branch office.
Type / Material No. / Serial No.: ...................................................................................