Philips M2540 User Manual download pdf (Page 5)

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

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