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:
Part number:
© 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
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
71034 Boeblingen, Germany
(+49)
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
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.
P hili ps Me dical Sy stems
M3860A/M3861A HEARTSTART FR2+