KISSTM / KISSTM Multilead Electrode Application System Service Manual 22745010 Revision H

GE Healthcare

KISS™ / KISS™ Multilead Electrode Application System Service Manual

22745010 Revision H

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.

Table Caption: This table provides a revision history of a document, detailing each revision level, its effective date, and a summary of the changes made, including specific ECO numbers and page references. It tracks the evolution of the document from its initial release in September 1996 through various updates and additions up to 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.

The use of ACCESSORY equipment not complying with the equivalent safety requirements of this equipment may lead to a reduced level of safety of the resulting system. Consideration relating to the choice shall include:

• use of the accessory in the PATIENT VICINITY; and
• evidence that the safety certification of the ACCESSORY has been performed in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1harmonized national standard.

The authorized representative for GE Medical Systems Information Technologies Inc. in Europe is :

GE Medical Systems Information Technologies GmbH

Munzinger Strasse 5

79111 Freiburg

GERMANY

Phone +49-761 4543 0

Fax +49-761 4543 233

Warnings, Cautions, and Notes

The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance.

Hazard is defined as a source of potential injury to a person.

DANGER

Indicates an imminent hazard which, if not avoided, will result in death or serious injury.

WARNING

Indicates a potential hazard or unsafe practice which, if not avoided, could result in death or serious injury.

CAUTION

Indicates a potential hazard or unsafe practice which, if not avoided, could result in minor personal injury or product/property damage.

NOTE

Provides application tips or other useful information to assure that you get the most from your equipment.

Service Requirements

Follow the service requirements listed below.

• Refer equipment servicing to GE Healthcare's authorized service personnel only.
• Any unauthorized attempt to repair equipment under warranty voids that warranty.
• It is the user's responsibility to report the need for service to GE Healthcare or to one of their authorized agents.
• Failure on the part of the responsible individual, hospital, or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.
• Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be functional when required.

Service Manual Language Information

**Table Caption: This table presents a warning about a service manual being available only in English, with corresponding translations of the warning in Bulgarian,