Welch Allyn Medical Diagnostic Equipment SCANTEAM 5770 ユーザーズマニュアル

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Disclaimer
Welch Allyn

 reserves the right to make changes in specifications and
other information contained in this document without prior notice, and the
reader should in all cases consult Welch Allyn to determine whether any
such changes have been made.  The information in this publication does
not represent a commitment on the part of Welch Allyn.
Welch Allyn shall not be liable for technical or editorial errors or
omissions contained herein; nor for incidental or consequential
damages resulting from the furnishing, performance, or use of this
material.
This document contains proprietary information which is protected by
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prior written consent of Welch Allyn, Incorporated.

 1999 Welch Allyn, Inc.  All rights reserved.
Welch Allyn shall not be liable for use of our product with equipment 
(i.e., power supplies, personal computers, etc.) that is not CE marked and
does not comply with the Low Voltage Directive.
The CE mark on the product indicates that the system has been tested to and
conforms with the provisions noted within the 89/336/EEC Electromagnetic
Compatibility Directive and the 73/23/EEC Low Voltage Directive.
C.S.A. Statement
This product must be used with a certified Class 2 power
supply or be powered by a certified SELV (Safety Extra Low
Voltage) output.
RF Approvals
This product complies with the following:
U.S.A.
FCC Part 15.249 Certified
Australia
C–TIC
Canada
RSS 210 Certified
Europe
ETS 300 328 Certified
Mexico
NOM–EM–121–SCT1–1994 Certified
Singapore
Type Approval for Spread Spectrum System
Safety Approvals
U.S.A.
UL Listed, C22.2 No. 950 / UL 1950
Australia
conforms to AS/NZS 
Canada
3548cUL Listed
Europe
TÜV Rheinland GS Licensed, EN 60950 
(IEC 950) (Scanner and Base only, not on battery)
Mexico
NYCE Certified, NOM 19