Philips HEARTSTART XLT M3500B - Manual (Page 4)

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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.