GE KISS Service Manual page 2

Publication Information
The information in this manual applies only to KISS /KISS Mlutilead . It does not apply to earlier product versions. Due to continuing product
innovation, specifications in this manual are subject to change without notice.
KISS, CASE and MAC are trademarks owned by GE Medical Systems Information Technologies, Inc., a General Electric Company going to
market as GE Healthcare. All other trademarks contained herein are the property of their respective owners.
The document part number and revision are at the bottom of each page. The revision identifies the document's update level. The revision
history of this document is summarized in the following table.
Date
Revision
-
September 1996
A January 2004
B
April 2006
C
July 2009
D June 2010
E
April 2011
F
March 2014
G August 2014
H January 2017
To access other GE Healthcare Diagnostic Cardiology manuals, go to the Common Documentation Library (CDL), located at
http://www.gehealthcare.com/usen/service/biomed_tech_selfservice/services_user_doc/products/support.html, and click Cardiology.
To access Original Equipment Manufacturer (OEM) manuals, go to the device manufacturer's Web site.
CAUTION:
During repairs/service interventions, observe the protective measures against damage due to ESD.
Manual Purpose
This manual supplies technical information for service representative and technical personnel so they can maintain the equipment to the
assembly level. Use it as a guide for maintenance and electrical repairs considered field repairable. Where necessary the manual identifies
additional sources of relevant information and or technical assistance.
See the operator manual for the instructions necessary to operate the equipment safely in accordance with its function and intended use.
Intended Audience
This manual is intended for the person who uses, maintains, or troubleshoots this equipment.
Safety Information
Responsibility of the Manufacturer
GE Healthcare is responsible for the effects of safety, reliability, and performance only if:
• Assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons authorized by GE Healthcare.
• The electrical installation of the relevant room complies with the requirements of the appropriate regulations.
• The equipment is used in accordance with the instructions for use.
• The country of manufacture appears on the device label.
General
This device is not intended for home use.
Contact GE Healthcare for information before connecting any devices to the equipment that are not recommended in this manual.
Parts and accessories used must meet the requirements of the applicable IEC 601 series safety standards, and/or the system configuration
must meet the requirements of the IEC 60601-1-1 medical electrical systems standard.
Periodically, and whenever the integrity of the device is in doubt, test all functions.
2
Comments
Initial release.
ECO 07578
ECO 082331
ECO 096124
TM symbol for KISS added, changes on pages 3, 4, 21, 22, 28,
changes on pages 20 and 29, new section 3.5.4
Update of section 3.3.4 and chapter 6
•
Update of chapters 5 and 7 due to new RoHS-compliant AC suction pump
•
Removal of KISS-3 from FSM
Added information for the O-Rings.
KISS™ / KISS™ Multilead
22745010H
January 2017