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Philips M3860A User Manual

Page 6

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M3860A/M3861A HEARTSTART FR2+

Instructions for Use

Equipment specifications are subject to alteration

without notice. All changes will be in compliance

with regulations governing manufacture of

medical equipment.

Printed in the U.S.A.

Publication date: August 2003

Publication number: M3860-91900

Part number: 011120-0010

© 2003 Philips Electronics North America Corp.

No part of this publication may be reproduced,

transmitted, transcribed, stored in a retrieval

system or translated into any human or computer

language in any form by any means without the

consent of the copyright holder.

Unauthorized copying of this publication may not

only infringe copyright but also reduce the ability

of Philips Medical Systems to provide accurate

and up-to-date information to users and operators

alike.

Philips Medical Systems reserves the right to

make changes in specifications or to discontinue

any product at any time without notice or

obligation and will not be liable for any

consequences resulting from the use of this

publication.

Authorized EU Representative

Philips Medizinsysteme Boeblingen GmbH

Hewlett-Packard Strasse 2

71034 Boeblingen, Germany

(+49) 7031-14-5151

CAUTION

FEDERAL LAW (USA) RESTRICTS THIS DEVICE TO SALE

BY OR ON THE ORDER OF A PHYSICIAN.

The HeartStart FR2+ is designed to be used only with Philips-

approved accessories. The HeartStart FR2+ may perform

improperly if non-approved accessories are used.

Device Tracking

In the U.S.A., this device is subject to tracking requirements by

the manufacturer and distributors. If the defibrillator has been

sold, donated, lost, stolen, exported, or destroyed, notify Philips

Medical Systems or your distributor.

Device Manufacturer

The HeartStart FR2+ Defibrillator is manufactured by Philips

Medical Systems, Seattle, Washington, USA.

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