Brilliance CT: 6 / 1 0 / 1 6 / 1 6 P o W e R, 4 0 / 6 4 - C H A N N e L, Big Bore Configuration

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Brilliance CT TM

6/10/16/16 Power, 40/64-Channel,


Big Bore Configuration
ADM Failure Report

4550 199 04071 Revision E

Philips Medical Systems


© 2007 KONINKLIJKE PHILIPS ELECTRONICS N. V. ALL RIGHTS RESERVED.

Warranty Disclaimer
PHILIPS PROVIDES THIS DOCUMENT WITHOUT WARRANTY OF ANY KIND, IMPLIED OR EXPRESSED, INCLUDING, BUT NOT LIMITED TO,
THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE.

Limitation of Liability
PHILIPS HAS TAKEN CARE TO ENSURE THE ACCURACY OF THIS DOCUMENT. HOWEVER, PHILIPS ASSUMES NO LIABILITY FOR
ERRORS OR OMISSIONS AND RESERVES THE RIGHT TO MAKE CHANGES WITHOUT FURTHER NOTICE TO ANY PRODUCTS HEREIN TO
IMPROVE RELIABILITY, FUNCTION, OR DESIGN. PHILIPS MAY MAKE IMPROVEMENTS OR CHANGES IN THE PRODUCT(S) OR
PROGRAM(S) DESCRIBED IN THIS DOCUMENT AT ANY TIME.

Revision History

ECO # Revision Date Comments


R61040022 01 September 2004 New Release
H2011333 B July 2005 Added Brilliance 64
H2012746 C January 2006 Updated Format and added Big Bore
H3000215 D September 2006 Added table: order of modules in faulty 6/7 pack
H3000639 E March 2007 Update format and added BR 64-channel with TDMS
This document was prepared by the CT PMG Haifa Service Innovation Department.
For any additions, corrections, or suggestions, contact:
CT PMG Haifa Customer Support Department
Email: helpdesk.ct.haifa@philips.com

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems (“Philips”) and may not be
reproduced, copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal
Department. Use of this document and the information contained in it is strictly reserved for current Philips personnel and Philips customers who have
a current and valid license from Philips for use by the customer’s designated in-house service employee on equipment located at the customer’s
designated site. Use of this document by unauthorized persons is strictly prohibited. Report violation of these requirements to the Philips Legal
Department. This document must be returned to Philips when the user is no longer licensed and in any event upon Philips’ first written request.

© 2007 Philips Medical Systems


Detector Module Failure Report
NOTE For the repair and replace procedures refer to the
Troubleshooting and Replacement Manual found at the InCenter.
Fill in this form with as much detail as possible and send it with the returned module/s.
• Circle the relevant system from the list below and enter the required data.
System Type: Brilliance 10/16 (water), Mx8000 IDT, Brilliance (air) 6 / 10 / 16 / 16P /40 / 64 / 64 (with TDMS) / Big Bore
FSE Name: Date:
FSE Telephone #: DMS S/N:
Site Name: Faulty module S/N:
System S/N: Faulty module position:
• If you replaced a set of 6 modules (7 in Big Bore) write down the serial numbers of removed modules.
Module Position on DMS 19 20 21 22 23 24

Module Position on DMS


23 24 25 26 27 28 29
(Big Bore)

Module SN

• Fill in the Slice #, Row # in Module, and Detector # in the DMS and circle the relevant symptom(s) in
each Failure Property for the Detector Module (ADM):

Slice # (or range): Artifacts on


Color Appearance Test
Row # in Module: Image
Detector # in the DMS: Band Black Permanent Noise
Ring White Intermittent Leakage
Dot Bad Detector
Streak Partial Volume
Not Tested
Other:

• Did Air Calibration improve/correct the ring? Y/N If Yes, for how long? ______________
• Write the Scan Parameters when failure appears or circle “Any Scan”
Scan Type (Axial / Spiral): Resolution
Scan Category (e.g. Ear, Spine) Collimation
Thickness Pitch
kV Rotation Time
mAs
Any Scan
Comments:

CSIP Level 1 © 2007 Koninklijke Philips Electronics N.V All Rights Reserved Refer to Front Cover

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