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SIST EN 60601-2-13:2006/A1:2008

(Amendment)

Medical electrical equipment -- Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems

Medical electrical equipment -- Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems

Superseded by EN ISO 80601-2-13:2012 (the DOW of which is 2015-12-31)

Medizinische elektrische Geräte -- Teil 2-13: Besondere Festlegungen für die Sicherheit von Anästhesiesystemen

Appareils électromédicaux -- Partie 2-13: Règles particulières de sécurité et performance essentielle pour les systèmes d'anesthésie

Medicinska električna oprema - 2-13. del: Posebne varnostne zahteve in bistvene lastnosti sistemov za anestezijo (IEC 60601-2-13:2003/A1:2006)

General Information

Status
Withdrawn
Publication Date
27-Nov-2007
Withdrawal Date
17-Jan-2016
ICS
11.040.10 - Anaesthetic, respiratory and reanimation equipment
Technical Committee
IEMO - Electrical equipment in medical practice
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
14-Jan-2016
Due Date
06-Feb-2016
Completion Date
18-Jan-2016
Directive
93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Ref Project
EN 60601-2-13:2006/A1:2007 - Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems

Relations

Amends
SIST EN 60601-2-13:2006 - Medical electrical equipment -- Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems
Effective Date
01-Feb-2008
Replaced By
SIST EN ISO 80601-2-13:2013 - Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation (ISO 80601-2-13:2011)
Effective Date
01-Mar-2013
Amends
SIST EN 60601-2-13:2006 - Medical electrical equipment -- Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems
Effective Date
29-Jan-2023

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-2-13:2006/A1:2008
01-februar-2008
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQHYDUQRVWQH]DKWHYHLQELVWYHQH
ODVWQRVWLVLVWHPRY]DDQHVWH]LMR ,(&$
Medical electrical equipment - Part 2-13: Particular requirements for the safety and
essential performance of anaesthetic systems (IEC 60601-2-13:2003/A1:2006)
Medizinische elektrische Geräte - Teil 2-13: Besondere Festlegungen für die Sicherheit
von Anästhesiesystemen (IEC 60601-2-13:2003/A1:2006)
Appareils électromédicaux - Partie 2-13: Regles particulieres de sécurité et performance
essentielle pour les systemes d'anesthésie (IEC 60601-2-13:2003/A1:2006)
Ta slovenski standard je istoveten z: EN 60601-2-13:2006/A1:2007
ICS:
11.040.10
SIST EN 60601-2-13:2006/A1:2008 en,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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

EUROPEAN STANDARD
EN 60601-2-13/A1

NORME EUROPÉENNE
March 2007
EUROPÄISCHE NORM

ICS 11.040.10


English version


Medical electrical equipment -
Part 2-13: Particular requirements for the safety
and essential performance of anaesthetic systems
(IEC 60601-2-13:2003/A1:2006)


Appareils électromédicaux -  Medizinische elektrische Geräte -
Partie 2-13: Règles particulières Teil 2-13: Besondere Festlegungen
de sécurité et performance essentielle für die Sicherheit
pour les systèmes d'anesthésie von Anästhesiesystemen
(CEI 60601-2-13:2003/A1:2006) (IEC 60601-2-13:2003/A1:2006)




This amendment A1 modifies the European Standard EN 60601-2-13:2006; it was approved by CENELEC on
2007-03-01. 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, Bulgaria, 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


© 2007 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-2-13:2006/A1:2007 E

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

EN 60601-2-13:2006/A1:2007 - 2 -
Foreword
The text of amendment 1:2006 to the International Standard IEC 60601-2-13:2003, prepared by SC 62D,
Electromedical equipment, of IEC TC 62, Electrical equipment in medical practice, was submitted to the
Unique Acceptance Procedure and was ap
...

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