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IEC 60601-2-13 Ed. 3.1 Edition 08/2009
Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems
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Abstract

IEC 60601-2-13:2003+A1:2006(E) specifies particular safety and essential performance requirements for individual devices designed for use in an anaesthetic system as well as specific requirements for the anaesthetic gas delivery system. This standard specifies requirements and defines interfaces for:
- individual devices designed for use in an anaesthetic systems(s), and
- integrated anaesthetic systems.
This consolidated version consists of the third edition (2003) and its amendment 1 (2006). Therefore, no need to order amendment in addition to this publication.

Status

Standard - Active

Origin

Technical Committee :
62D : Electromedical equipment

Implementation

start of the vote on the project      date of ratification (dor)   
end of the vote on the project      date of anouncement (doa)   
start of the vote on the final project      date of publication (dop)   
end of the vote on the final project      date of withdrawal (dow)   


Publication Official Journal
of the Grand-Duchy of Luxembourg
Reference

International Classification for Standards (ICS codes) :

11.040.10 : Anaesthetic, respiratory and reanimation equipment

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