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M2540-92000-01 A M2540 Ultrasound System Field Service Manual Page 5
About This Manual: About This Manual
© 2002 Philips North America
Corporation
All Rights Reserved.
Reproduction in whole or part
is prohibited without the prior
written consent of the copyright
holder.
Publication number
M2540-98000-01
Edition 1
Published: December 2002
Printed in U.S.A.
Warranty
The information contained in
this document is subject to
change without notice.
Philips Medical Systems makes
no warranty of any kind with
regard to this material,
including, but not limited to, the
implied warranties or
merchantability and fitness for a
particular purpose.
Philips Medical Systems shall
not be liable for errors
contained herein or for
incidental or consequential
damages in connection with the
furnishing, performance,
or use of this material.
Trademarks
Cannon is a registered
trademark of Cannon
Corporation.
Windows XP is a trademark of
Microsoft Corporation
WARNING
Electrical Shock Hazard
Do not remove system covers.
To avoid electrical shock, use
only supplied power cords and
connect only to properly
grounded (3-hole) wall outlets.
Explosion Hazard
Do not operate the system in the
presence of flammable
anesthetics.
Safety Information
Before you use a specialty
transducer for the first time, be
sure to read the “Description
and Use” section of the chapter
that is applicable to your
transducer. Also, for TEE and
intraoperative transducers,
review the “Electrical Safety”
sections in those chapters.
Pay special attention to the
Warnings and Cautions.
The warnings explain the
dangers of electrical shock and
explosion hazard, the safety of
ultrasound, applications,
guidelines for fetal use, and
guidelines for setting controls
that affect acoustic output and
accuracy of clinical
measurements.
Warning Symbol Used in the
Text:
WARNING
The cautions explain potential
damage to equipment.
Caution Symbol Used in the
Text:
Symbols on the System
Warning symbols, as well as
other symbols appearing on the
system or its probes:
This symbol on the
system advises
operators to consult
the user documentation for that
part of the system.
This symbol on the
system indicates a
potential for
electrical shock.
Monitor Radiation
The monitor used in this
system complies with the FDA
regulations that were
applicable at the date of
manufacture (21 CFR
Subcategory J).
Prescription Device
The United States Food and
Drug Administration requires
the following labeling
statement:
Caution - Federal Law restricts
this device to use by or on the
CAUTION
!
Important
0123
marking is for
Council Directive
93/42/EEC.
This system complies with the
Medical Device Directive.
Authorized EU
Representative:
Philips Medizinsysteme
Boeblingen GmbH
Hewlett-Packard Strasse 2
71034 Boeblingen, Germany