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About This Edition
Edition 1
Printed in the USA
Publication number M4735-91900
The information in this guide applies to
the M4735A Heartstream XL, release
A.00. This information is subject to
change without notice.
Agilent Technologies shall not be liable
for errors contained herein or for inci-
dental or consequential damages in con-
nection with the furnishing,
performance, or use of this material.
Edition History
Edition 1, September, 2000
Copyright
Copyright © 2000
Agilent Technologies, Inc.
3000 Minuteman Road
Andover, MA USA 01810-1099
(978) 687-1501
This document may not be photocopied,
reproduced, or translated to another lan-
guage without prior written consent of
Agilent Technologies.
SMART Biphasic is a registered
trademark of Agilent Technologies.
Use of supplies or accessories other
than those recommended by Agilent
Technologies 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 PHYSICIAN.
Medical Device Directive
The M4735A Heartstream XL Defibril-
lator/Monitor complies with the
requirements of the Medical Device
Directive 93/42/EEC and carries the
0123
mark accordingly.
Authorized EU-representative:
Agilent Technologies
Deutschland GmbH
Herrenbergerstr.130
D 71034 Boeblingen, Germany
Fax: +49-7031-14-2346
Warning
Radio frequency (RF) interference from
nearby transmitting devices may
degrade the performance of the
M4735A Heartstream XL Defibrillator/
Monitor. Electromagnetic compatibil-
ity with surrounding devices should be
assessed prior to using the defibrillator/
monitor.
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