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CodeMaster XL+ (M1722B) Defibrillator/Monitor

Service Manual

Printed in USA HP Part Number: M1722-91909 Print Date: May 16, 2000 Edition 6

May 22, 2000 11:08 am DRAFT

Notice
About This Edition
Publication number M1722-91909 Edition 6 Printed in USA

WARNING
As with electronic equipment, Radio Frequency (RF) interference between the defibrillator and any existing RF transmittingor receiving equipment at the installation site, including electrosurgical equipment, should evaluated carefully and any limitations noted before the equipment is placed in service Monitoring during quiescent periods of electrosurgery is possible but electromagnetic interference generated by electrosurgical tools during operation is sufficient to mask cardiac signals. A momentary recovery periodis required for the monitor to return to normal operation and will be longer if the diagnostic monitoring mode is used. Pads or electrodes should be placed as far from the surgical area as reasonable while still performing normal function to minimize the possibility of burns. Radio frequency generation from electrosurgical equipment and close proximity transmitters may seriously degrade performanceof the CodeMaster XL+ defibrillator/monitor. Hewlett-Packard assumes no liability for failures resulting from RF interference between HP medical electronics and any radio frequency generating equipment at levels exceeding those established by applicable standards. Classified by Underwriters Laboratories, Inc. with respect to electrical shock, fire, and mechanical hazards only in accordance withUL 2601-1.

Responsibility of Manufacturer
Hewlett-Packard only considers itself responsible for any effects on safety, reliability and performance of the CodeMaster XL+ defibrillator/monitor and the battery support system if: assembly operations, extensions, readjustments, modifications or repairs are done by persons authorized by Hewlett-Packard, and

Edition History
Edition 1, August 1992Edition 2, October 1992 Edition 3, February 1993 Edition 4, November 1994 Edition 5, August 1996 Edition 6, May 16, 2000

Copyright Copyright © 1992, 1993, 1994, 1996, 1998
Hewlett-Packard Company Andover, MA 01810 USA Authorized EU-representative: Hewlett-Packard GmbH Deutschland GmbH Herrenbergerstr.130 D 71034 Boeblingen, Germany Fax: +49-7031-14-2346 This information is subject to changewithout notice. Reproduction, adaptation, or translation without prior written permission is prohibited, except as allowed under the copyright laws.

the electrical installation of the relevant room or vehicle complies with the IEC or national requirements, and the instrument is used according to the instructions for use presented in this manual.

Medical Device Directive
This product complieswith the requirements of the Medical Device Directive 93/42/EEC and carries the CE mark accordingly. This product complies with the requirements of the EMC Directive 89/336/EEC and carries the CE mark accordingly.

CAUTION
The manufacturer, importer and seller are responsible for the effects on safety, reliability and performance only if: assembly operations, extensions, re-adjustments,modifications or repair are carried out by persons authorized by them, and the electrical installation of the relevant room complies with all local regulations and the equipment is used in accordance with the instructions for use. Use of accessories other than those recommended by Hewlett-Packard may compromise product performance. THIS PRODUCT IS NOT INTENDED FOR HOME USE.

Warranty
Hewlett-Packardmakes no warranty of any kind with regard to this material, included, but not limited to, the implied warranties or merchantability and fitness for a particular purpose. Hewlett-Packard shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. This product may contain remanufactured parts...