Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests

D129/100: To be offered to EC for publication in the OJEC under the MDD

Medizinische elektrische Geräte - Teil 1-2: Allgemeine Festlegungen für die Sicherheit - Ergänzungsnorm: Elektromagnetische Verträglichkeit - Anforderungen und Prüfungen

Appareils électromédicaux - Partie 1-2: Règles générales de sécurité - Norme collatérale: Compatibilité électromagnétique - Exigences et essais

Medicinska električna oprema – 1-2. del: Splošne varnostne zahteve – Spremljevalni standard: Elektromagnetna združljivost – Zahteve in preskusi (IEC 60601-1-2:2001/A1:2004)

General Information

Status
Withdrawn
Publication Date
28-May-2006
Withdrawal Date
28-Feb-2009
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
01-Jun-2012
Completion Date
01-Jun-2012

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Standards Content (Sample)

EUROPEAN STANDARD
EN 60601-1-2/A1

NORME EUROPÉENNE
May 2006
EUROPÄISCHE NORM

ICS 11.040.01; 33.100.10; 33.100.20


English version


Medical electrical equipment
Part 1-2: General requirements for safety -
Collateral standard: Electromagnetic compatibility -
Requirements and tests
(IEC 60601-1-2:2001/A1:2004)


Appareils électromédicaux Medizinische elektrische Geräte
Partie 1-2: Règles générales de sécurité - Teil 1-2: Allgemeine Festlegungen
Norme collatérale: für die Sicherheit -
Compatibilité électromagnétique - Ergänzungsnorm:
Exigences et essais Elektromagnetische Verträglichkeit -
(CEI 60601-1-2:2001/A1:2004) Anforderungen und Prüfungen
(IEC 60601-1-2:2001/A1:2004)




This amendment A1 modifies the European Standard EN 60601-1-2:2001; it was approved by CENELEC on
2006-03-01. CENELEC members are bound to comply with the CEN/CENELEC Internal Regulations which
stipulate the conditions for giving this amendment the status of a national standard without any alteration.

Up-to-date lists and bibliographical references concerning such national standards may be obtained on
application to the Central Secretariat or to any CENELEC member.

This amendment exists in three official versions (English, French, German). A version in any other language
made by translation under the responsibility of a CENELEC member into its own language and notified to the
Central Secretariat has the same status as the official versions.

CENELEC members are the national electrotechnical committees of Austria, Belgium, Cyprus, the Czech
Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain,
Sweden, Switzerland and the United Kingdom.

CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung

Central Secretariat: rue de Stassart 35, B - 1050 Brussels


© 2006 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-1-2:2001/A1:2006 E

---------------------- Page: 1 ----------------------

EN 60601-1-2:2001/A1:2006 - 2 -

Foreword
The text of document 62A/462/FDIS, future amendment 1 to IEC 60601-1-2:2001, prepared by
IEC TC 62, Electrical equipment in medical practice, was submitted to the IEC-CENELEC parallel vote
and was approved by CENELEC as amendment A1 to EN 60601-1-2:2001 on 2006-03-01.
The following dates were fixed:
– latest date by which the amendment has to be
implemented at national level by publication of
(dop) 2006-12-01
an identical national standard or by endorsement
– latest date by which the national standards conflicting
(dow) 2009-03-01
with the amendment have to be withdrawn
__________
Endorsement notice
The text of amendment 1:2004 to the International Standard IEC 60601-1-2:2001 was approved by
CENELEC as an amendment to the European Standard without any modification.
__________

---------------------- Page: 2 ----------------------

NORME CEI
INTERNATIONALE
IEC



60601-1-2
INTERNATIONAL


2001
STANDARD


AMENDEMENT 1
AMENDMENT 1

2004-09

Amendement 1
Appareils électromédicaux –
Partie 1-2:
Règles générales de sécurité –
Norme collatérale:
Compatibilité électromagnétique –
Exigences et essais

Amendment 1
Medical electrical equipment –
Part 1-2:
General requirements for safety –
Collateral standard:
Electromagnetic compatibility –
Requirements and tests
 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
CODE PRIX
S
Commission Electrotechnique Internationale
PRICE CODE
International Electrotechnical Commission
МеждународнаяЭлектротехническаяКомиссия
Pour prix, voir catalogue en vigueur
For price, see current catalogue

---------------------- Page: 3 ----------------------

60601-1-2 Amend. 1  IEC:2005 – 3 –
FOREWORD
This amendment has been prepared by subcommittee 62A: Common aspects of electrical
equipment used in medical practice, of IEC technical committee 62: Electrical equipment in
medical practice.
This bilingual version (2005-09) replaces the English version.
The text of this amendment is based on the following documents:
FDIS Report on voting
62A/462/FDIS 62A/469/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 French version of this amendment fas not been voted upon.
The committee has decided that the contents of this amendment and the base publication will
remain unchanged until the maintenance result
...

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