EN 60601-2-13:2006/A1:2007
(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Superseded by EN ISO 80601-2-13:2012 (the DOW of which is 2015-12-31)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- Withdrawn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
- 15-Mar-2007
- Withdrawal Date
- 30-Dec-2015
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62D - IEC_SC_62D
- Parallel Committee
- IEC/SC 62D - IEC_SC_62D
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 31-Dec-2015
- Completion Date
- 31-Dec-2015
Relations
- Effective Date
- 29-Jan-2023
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Frequently Asked Questions
EN 60601-2-13:2006/A1:2007 is a amendment published by CLC. Its full title is "Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems". This standard covers: Superseded by EN ISO 80601-2-13:2012 (the DOW of which is 2015-12-31)
Superseded by EN ISO 80601-2-13:2012 (the DOW of which is 2015-12-31)
EN 60601-2-13:2006/A1:2007 is classified under the following ICS (International Classification for Standards) categories: 11.040.10 - Anaesthetic, respiratory and reanimation equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-13:2006/A1:2007 has the following relationships with other standards: It is inter standard links to EN 60601-2-13:2006. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-13:2006/A1:2007 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/432. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
EN 60601-2-13:2006/A1:2007 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
SLOVENSKI STANDARD
01-februar-2008
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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
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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
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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