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XPW7-000 834 01 01 02

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Mammography Systeme

Safety-Related Tests Report


System
Safety Check per IEC 62353:2014-09

Customer:

Address:

Fax / E-Mail:
Fax / E-Mail:

Department: Room:
Material-No.: Serial-No.:
Contract-No.: Expire date:
Order-No.: System - ID:

The instructions XPW7-000.833.01.01.XX are required for this protocol


2 Report Date: Serial-No.:

Final Evaluation
Initial Measurement Repeat Measurement

The evaluation was performed after completing all work steps.


No deficiencies
Slight deficiencies that require corrective measures. These must be recorded
under Remarks.
Significant deficiencies: The safety of the system is no longer assured. If these
deficiencies are not corrected, there is a "risk for patients, users or third par‐
ties".

Signature:

Date: Tester:

If required by country-specific regulations:


The customer or a representative has taken note of the result of the evaluation of the
system condition.

Signature:

Date: Name:

Remarks:

Mammography Systeme XPW7-000.834.01.01.02 Page 2 of 6 © Siemens, 2017


09.17 CS SLM XP PDM
Report Date: Serial-No.: 3

Remarks regarding the Protocol


The chapter numbers refer to the chapters in the instruction, which is referenced on the
cover page.
All pages have to have the serial number of the system and the date of maintenance in
the page header.
The abbreviation n.a. (not applicable) indicates that the test item or measured value does
not apply to this system.
On page 2 the completeness and the results of the maintenance work is confirmed.

Explanation of Abbreviations in the Report

Abbrev. Explanation Abbrev. Explanation


SI Safety Inspection SIE Electrical Safety Inspection
SIM Mechanical Safety Inspection CSE Customer Service Engineer

© Siemens, 2017 XPW7-000.834.01.01.02 Page 3 of 6 Mammography Systeme


09.17 CS SLM XP PDM
4 Report Date: Serial-No.:

Measuring Equipment and Measuring Instruments Used


Measuring instruments and measuring devices (phantoms, MR coils, etc.) may not be en‐
tered in the table if they have already been entered in the mobile device.

Measuring equipment / -instruments Serial No. Date Used

Mammography Systeme XPW7-000.834.01.01.02 Page 4 of 6 © Siemens, 2017


09.17 CS SLM XP PDM
Report Date: Serial-No.: 5
OK not n.a.
OK

1 General Notes
1.5 Reason for the checks
Q The check is performed as a safety check.
Q The check is performed during startup.
Q The check is performed after a repair.
Q The check is performed during maintenance.

2 Testing and inspection


2.1 Visual inspection
2.1.1 System inspections
SI Check of the “complete and current” documents.
SI Check of externally accessible fuses.
SI Check of the safety-related markings.
SI Check of the safety-related markings.
SI Damage check.
SI Check of contamination.
2.1.2 Inspections of relevant accessories
SI Check of relevant accessories.

2.3 Grounding conductor measurement


SIE Ground wire status (in milliohms)

value:
2.4 Device leakage current measurement on the AWS
SIE Device leakage current (in milli A)

value:

SIE Equivalent leakage current (in milli A).

value:
2.5 Function check
SIE Perform a function check.

Check of this section was performed by:

Signature:

Date: Name:

© Siemens, 2017 XPW7-000.834.01.01.02 Page 5 of 6 Mammography Systeme


09.17 CS SLM XP PDM
All documents may only be used for
rendering services on Siemens
Healthcare Products. Any document
in electronic form may be printed
once. Copy and distribution of elec‐
tronic documents and hardcopies is
prohibited. Offenders will be liable
for damages. All other rights are re‐
served.

healthcare.siemens.com/services

Siemens Healthineers Headquarters


Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
Telephone: +49 9131 84-0
siemens.com/healthineers

Print No.: XPW7-000.834.01.01.02 | Replaces: n.a.


Doc. Gen. Date: 09.17 | Language: English
© Siemens Healthcare GmbH, 2017

siemens.com/healthineers

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