Amendment 2 - Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

General Information

Status
Published
Publication Date
27-Nov-2005
Current Stage
DELPUB - Deleted Publication
Completion Date
09-Aug-2007
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IEC 60601-2-37:2001/AMD2:2005 - Amendment 2 - Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment Released:11/28/2005 Isbn:2831883822
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INTERNATIONAL IEC
STANDARD 60601-2-37
AMENDMENT 2
2005-11
Amendment 2
Medical electrical equipment –
Part 2-37:
Particular requirements for the safety
of ultrasonic medical diagnostic
and monitoring equipment
 IEC 2005 Droits de reproduction réservés  Copyright - all rights reserved
International Electrotechnical Commission, 3, rue de Varembé, PO Box 131, CH-1211 Geneva 20, Switzerland
Telephone: +41 22 919 02 11 Telefax: +41 22 919 03 00 E-mail: inmail@iec.ch Web: www.iec.ch
PRICE CODE
Commission Electrotechnique Internationale C

International Electrotechnical Commission
МеждународнаяЭлектротехническаяКомиссия
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– 2 – 60601-2-37 Amend. 2  IEC:2005(E)

FOREWORD
This amendment has been prepared by subcommittee 62B: Diagnostic imaging equipment, of

IEC technical committee 62: Electrical equipment in medical practice.

The text of this amendment is based on the following documents:

FDIS Report on voting
62B/591/FDIS 62B/598/RVD
Full information on the voting for the approval of this amendment can be found in the report

on voting indicated in the above table.
The committee has decided that the contents of this publication will remain unchanged until
the maintenance result date indicated on the IEC web site under "http://webstore.iec.ch" in the
data related to the specific publication. At this date, the publication will be
• reconfirmed;
• withdrawn;
• replaced by a revised edition, or
• amended.
_____________
Page 8
1.3.101 Related international standards
Add, to the existing list, the following new standard.
ISO 14971:2000, Medical devices – Application of risk management to medical devices
Amendment 1 (2003)
Page 19
6.8.2 INSTRUCTIONS FOR USE
aa) Add, on page 20, to the existing list of items, the following new item:

14) declaration of output limits as s
...

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