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ILNAS-EN ISO 80601-2-13:2022 Edition 06/2022
Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation (ISO 80601-2-13:2022)
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Abstract

This document is applicable to the basic safety and essential performance of an anaesthetic workstation for administering inhalational anaesthesia whilst continuously attended by a professional operator. This document specifies particular requirements for a complete anaesthetic workstation and the following anaesthetic workstation components which, although considered as individual devices in their own right, may be utilized, in conjunction with other relevant anaesthetic workstation components, to form an anaesthetic workstation to a given specification: anaesthetic gas delivery system; anaesthetic breathing system; anaesthetic gas scavenging system (AGSS); anaesthetic vapour delivery system; anaesthetic ventilator; monitoring equipment; alarm system; protection device. NOTE 1        Monitoring equipment, alarm systems and protection devices are summarized in Table AA.1. An anaesthetic workstation supplied complete and its individual components are considered as ME equipment or ME systems with regard to the general standard. NOTE 2        The applicability of this document is indicated in Table AA.2. This document is also applicable to those accessories intended by their manufacturer to be connected to an anaesthetic workstation where the characteristics of those accessories can affect the basic safety and essential performance of the anaesthetic workstation. If a clause or subclause is specifically intended to be applicable to anaesthetic workstation components or its accessories only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to an anaesthetic workstation and its individual components including accessories, as relevant. Hazards inherent in the intended physiological function of an anaesthetic workstation and its individual components including accessories within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1. NOTE 3        See also IEC 60601-1:2005+AMD1:2012+AMD2:2020, 4.2. This document is not applicable to any anaesthetic workstation intended for use with flammable anaesthetic agents, as determined by Annex BB.

Status

Standard - Active

Origin

Technical Committee :
CEN/TC 215 : Respiratory and anaesthetic equipment

Implementation

start of the vote on the project    05/09/2019   date of ratification (dor)    25/05/2022
end of the vote on the project    26/11/2019   date of anouncement (doa)    30/09/2022
start of the vote on the final project    16/12/2021   date of publication (dop)    31/12/2022
end of the vote on the final project    13/02/2022   date of withdrawal (dow)    30/06/2025


Publication Official Journal
of the Grand-Duchy of Luxembourg
14/12/2022
Reference Mémorial A N° 623

Relations

Evolutions

Relations to older standards
ILNAS-EN ISO 80601-2-13:2012/A2:2019
ILNAS-EN ISO 80601-2-13:2012/A1:2019
ILNAS-EN ISO 80601-2-13:2012

Relations to international standards
ISO 80601-2-13:2022 
ISO 80601-2-13 

International Classification for Standards (ICS codes) :

11.040.10 : Anaesthetic, respiratory and reanimation equipment

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