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Philips PDF
Juno DRF
FIELD SAFETY NOTICE Ref. Number: FSN70900021
CUSTOMER INFORMATION LETTER Ref. Number: N/A
TITLE: Update for Air Kerma Software
Document history
Revision Revision date Created/changed by Description
1.0 August 2013 F. Schwegat Original version
Applies to
CSIP Level 1
ATTENTION: This page contains copyrighted materials that are confidential and/or proprietary.
Any release or distribution of this material, without permission, is a violation of law.
© 2013 Koninklijke Philips N.V. ALL RIGHTS RESERVED
Effective template: XI-DXR-200-4002, Revision 2.0
Remote Software Installation
4 Introduction
Symptom
The air kerma (AKR) display is incorrect and unstable for zoom mode 30 × 30 cm (12 × 12") and 15
×15 cm (6 ×6") during continuous fluoroscopy only. All other modes operate as expected. (Problem
report ID: 1965550)
Cause
Software bug in the generator.
Remedy
A new Generator CPU Power EPROM.
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7 Compliance Testing
Compliance testing: Yes
Manpower requirements: One service engineer (1.5 hours)
• To perform the compliance testing, refer to SMI Juno DRF (4512 988 0648x) > Setting-to-work >
Juno G configuration > AK (Air kerma) setup and calibrationchapter three in the README manual.
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Ordering Information
Order the indicated material/kit according to the standard local service logistic procedures.
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12 Procedure
This software update is applicable to Juno DRF systems already updated to “SP4” release.
• If the system is not upgraded to service pack 4, first upgrade the system with the Juno System serv-
ice pack 4 upgrade kit (4512 134 49131). Therefore carry out the FCO7090018 for North America or
the FCO70900020 for the ROW.
• Carry out this FCO as described in the README manual: “README Juno G AK fix PROM Rev. 24
Jul 2013.
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14 Parts Disposal
• Dispose of the old parts according to local environmental regulations.
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15 Documentation
• File the delivered README manual in the section "Service information > Field change orders (FCO)"
of the SRM.
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Proprietary Notice:
This document and the information contained in it is proprietary and confidential information of Philips Healthcare
("Philips") and may not be reproduced, copied in whole or in part, adapted, modified, disclosed to others, or disse-
minated without the prior written permission of the Philips Legal Department. Use of this document and the infor-
mation 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 lo-
cated at the customer’s designated site. Use of this document by unauthorized persons is strictly prohibited. Re-
port 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.
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.
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 reliabil-
ity, function, or design. Philips may make improvements or changes in the product(s) or program(s) described in
this document at any time.
Hospital / Address:
Product Number:
o Not completed as this unit is not affected per instruction because: (state reason)
______________________________________________
o Not completed because the customer refuses to install this FCO: (state reason)
______________________________________________
Signature Customer Services Manager Mail to: SSD Customer Services Manager
Glossary
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UAL Unit Affected List