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Philips Medical Systems
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.