Philips M3500B manual 1RWLFH

1RWLFH

About This Edition

Edition 3

Printed in the USA

Publication number M3500-91900

The information in this guide applies to the M3500B HeartStart XLT, release Main 35 and earlier. This information is subject to change without notice.

Philips Medical Systems shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, perfor- mance, or use of this material.

Edition History

Edition 1, January 3, 2000

Edition 2, May 15, 2000

Edition 3, October 30, 2002

Copyright

Copyright © 2002

Philips Electronics North America Corporation

3000 Minuteman Road Andover, MA USA 01810-1099 (978) 687-1501

All rights are reserved. Reproduction in whole or in part is prohibited without the prior written consent of the copy- right holder.

SMART Biphasic is a registered trade- mark of Philips Medical Systems.

Use of supplies or accessories other than those recommended by Philips Medical Systems may compromise product performance.

THIS PRODUCT IS NOT INTENDED FOR HOME USE.

IN THE U.S., FEDERAL LAW RESTRICTS THIS DEVICE TO SALE ON OR BY THE ORDER OF A PHY- SICIAN.

Medical Device Directive

The M3500B HeartStart XLT Defibril- lator/Monitor complies with the requirements of the Medical Device Directive 93/42/EEC and carries the

0123 mark accordingly.

Authorized EU-representative:

Philips Medizinsysteme Böblingen

GmbH

Hewlett Packard Str. 2

71034 Böblingen

Germany

Canada EMC:ICES-001

Device Tracking

In the USA, the Food and Drug Admin- istration requires defibrillator manufac- turers and distributors to track the location of their defibrillators. If your defibrillator has been sold, donated, lost, stolen, exported, or destroyed, or if it was not obtained directly from Philips Medical Systems, please notify Philips Medical Systems at (978) 659-3202.

ii