NF EN ISO 80601-2-13

NF EN ISO 80601-2-13

April 2013
Standard Current

Medical electrical equipment - Part 2-13 : particular requirements for basic safety and essential performance of an anaesthetic workstation

ISO/IEC 80601-2-13:2011 is applicable to the basic safety and essential performance of an anaesthetic workstation for administering inhalational anaesthesia whilst continuously attended by a professional operator. ISO/IEC 80601-2-13:2011 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; anaesthetic vapour delivery system; anaesthetic ventilator; monitoring equipment; alarm system; protection device.ISO/IEC 80601-2-13:2011 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 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, as relevant.Hazards inherent in the intended physiological function of an anaesthetic workstation and its individual components within the scope of ISO/IEC 80601-2-13:2011 are not covered by specific requirements in ISO/IEC 80601-2-13:2011 except in 7.2.13 and 8.4.1 of IEC 60601-1:2005.ISO/IEC 80601-2-13:2011 is not applicable to any anaesthetic workstation intended for use with flammable anaesthetic agents, as determined by Annex BB.

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Main informations

Collections

National standards and national normative documents

Publication date

April 2013

Release date

juin 2025 par NF EN ISO 80601-2-13 de 2013

Number of pages

133 p.

Reference

NF EN ISO 80601-2-13

ICS Codes

11.040.10   Anaesthetic, respiratory and reanimation equipment

Classification index

S95-186-2-13

Print number

1 - 12/03/2013

International kinship

European kinship

EN ISO 80601-2-13:2012
Sumary
Medical electrical equipment - Part 2-13 : particular requirements for basic safety and essential performance of an anaesthetic workstation

ISO/IEC 80601-2-13:2011 is applicable to the basic safety and essential performance of an anaesthetic workstation for administering inhalational anaesthesia whilst continuously attended by a professional operator.

ISO/IEC 80601-2-13:2011 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;
  • anaesthetic vapour delivery system;
  • anaesthetic ventilator;
  • monitoring equipment;
  • alarm system;
  • protection device.

ISO/IEC 80601-2-13:2011 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 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, as relevant.

Hazards inherent in the intended physiological function of an anaesthetic workstation and its individual components within the scope of ISO/IEC 80601-2-13:2011 are not covered by specific requirements in ISO/IEC 80601-2-13:2011 except in 7.2.13 and 8.4.1 of IEC 60601-1:2005.

ISO/IEC 80601-2-13:2011 is not applicable to any anaesthetic workstation intended for use with flammable anaesthetic agents, as determined by Annex BB.

Replaced standards (7)
NF EN ISO 8835-2
July 2009
Standard Cancelled
Inhalational anaesthesia systems - Part 2 : anaesthetic breathing systems

ISO 8835-2:2007 specifies requirements for anaesthetic breathing systems that are supplied either assembled by the manufacturer or for assembly by the user in accordance with the manufacturer's instructions. ISO 8835-2:2007 also covers circle absorber assemblies, exhaust valves, inspiratory and expiratory valves and, in some designs, those parts of an anaesthetic breathing system that are incorporated within an inhalation anaesthetic system, including the expiratory gas pathway of an anaesthetic ventilator.

NF EN ISO 8835-3
October 2009
Standard Cancelled
Inhalational anaesthesia systems - Part 3 : transfer and receiving systems of active anaesthetic gas scavenging systems

ISO 8835-3:2007 specifies requirements for transfer and receiving systems of active anaesthetic gas scavenging systems (active AGSSs) intended to reduce exposure of healthcare personnel to anaesthetic gases and vapours while providing patient protection (e.g. against excessive flow and pressure). ISO 8835-3:2007 also specifies requirements for transfer and receiving systems of active anaesthetic gas scavenging systems in which the power device is integral with the transfer and receiving system.

NF EN ISO 8835-3/A1
January 2011
Standard Cancelled
Inhalational anaesthesia systems - Part 3 : transfer and receiving systems of active anaesthetic gas scavenging systems

NF EN ISO 8835-4
July 2009
Standard Cancelled
Inhalational anaesthesia systems - Part 4 : anaesthetic vapour delivery devices

For the purposes of ISO 8835-4:2004, the requirements in IEC 60601-1:1988, Clause 1 apply except as follows. Addition: ISO 8835-4:2004 specifies particular requirements for the essential performance of anaesthetic vapour delivery devices (AVDDs), as defined in 3.1. ISO 8835-4:2004 is applicable to AVDDs which are a component of an anaesthetic system and are intended to be continuously operator-attended. ISO 8835-4:2004 gives specific requirements for AVDDs which are supplementary to the applicable general requirements in IEC 60601-2-13. ISO 8835-4:2004 is not applicable to AVDDs intended for use with flammable anaesthetics, as determined by Annex CC, and AVDDs intended for use within anaesthetic breathing systems (e.g. draw-over vaporizers). The requirements of ISO 8835-4:2004 which replace or modify the requirements of IEC 60601-1:1988 and its Amendments 1 (1991) and 2 (1995) are intended to take precedence over the corresponding general requirements.

NF EN ISO 8835-5
October 2009
Standard Cancelled
Inhalational anaesthesia systems - Part 5 : anaesthetic ventilators

ISO 8835-5:2004 specifies particular requirements for the essential performance of anaesthetic ventilators (as defined in 3.1). ISO 8835-5:2004 is applicable to anaesthetic ventilators which are always a component of an anaesthetic system and are intended to be continuously attended by an operator. ISO 8835-5:2004 is not applicable to anaesthetic ventilators intended for use with flammable anaesthetics, as determined by Annex BB. The requirements of ISO 8835-5:2004 which replace or modify the requirements of IEC 60601-1:1988 and its Amendments 1 (1991) and 2 (1995) are intended to take precedence over the corresponding general requirements. This Scope is additional to the Scope given in IEC 60601-1:1988, Clause 1, except as noted above.

NF EN 60601-2-13
February 2007
Standard Cancelled
Medical electrical equipment - Part 2-13 : particular requirements for the safety and essential performance of anaesthetic systems

Le présent document spécifie des exigences de sécurité et de performance essentielle pour un SYSTEME D'ANESTHESIE ainsi que pour les dispositifs individuels destinés à être utilisés dans un SYSTEME D'ANESTHESIE. Ce document entre dans le champ d'application de la Directive n°93/42/CEE du 14/06/1993 relative aux dispositifs médicaux.

NF EN 60601-2-13/A1
September 2007
Standard Cancelled
Medical electrical equipment - Part 2-13 : particular requirements for the safety and essential performance of anaesthetic systems

Le présent document modifie la norme NF EN 60601-2-13 de février 2007. Ce document entre dans le champ d'application de la Directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux.

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Table of contents
  • Avant-propos
    v
  • Introduction
    vi
  • 201.1 Domaine d'application, objet et normes connexes
    1
  • 201.2 Références normatives
    3
  • 201.3 Termes et définitions
    5
  • 201.4 Exigences générales
    10
  • 201.5 Exigences générales relatives aux essais des APPAREILS EM
    12
  • 201.6 Classification des APPAREILS EM et des SYSTEMES EM
    13
  • 201.7 Identification, marquage et documentation des APPAREILS EM
    13
  • 201.8 Protection contre des DANGERS d'origine électrique provenant des APPAREILS EM
    17
  • 201.9 Protection contre les DANGERS mécaniques des APPAREILS EM et des SYSTEMES EM
    18
  • 201.10 Protection contre des DANGERS dus aux rayonnements involontaires et excessifs
    19
  • 201.11 Protection contre les températures excessives et les autres DANGERS
    19
  • 201.12 Précision des commandes, des instruments et protection contre les caractéristiques de sortie présentant des risques
    22
  • 201.13 SITUATIONS DANGEREUSES et conditions de défaut
    27
  • 201.14 SYSTEMES ELECTROMEDICAUX PROGRAMMABLES (SEMP)
    28
  • 201.15 Construction de l'APPAREIL EM
    28
  • 201.16 SYSTEMES EM
    28
  • 201.17 Compatibilité électromagnétique des APPAREILS EM et des SYSTEMES EM
    29
  • 201.101 Exigences supplémentaires applicables aux SYSTEMES D'ADMINISTRATION DE GAZ ANESTHESIQUE
    29
  • 201.102 Exigences supplémentaires applicables à un SYSTEME D'ANESTHESIE PAR VOIE RESPIRATOIRE
    35
  • 201.103 Exigences supplémentaires applicables à une SYSTEME D'EVACUATION DES GAZ ANESTHESIQUES
    44
  • 201.104 Exigences supplémentaires applicables à un SYSTEME D'ADMINISTRATION DE VAPEUR ANESTHESIQUE
    48
  • 201.105 Exigences supplémentaires applicables à un ventilateur d'anesthesie
    53
  • 201.106 Boucles d'affichage
    59
  • 201.107 Évaluation clinique
    60
  • 202 Compatibilité électromagnétique - Exigences et essais
    60
  • 203 Exigences générales applicables à une radioprotection dans les appareils à rayonnement X de diagnostic
    60
  • 206 Aptitude à l'utilisation
    60
  • 208 Exigences générales, essais et guide pour les SYSTEMES D'ALARME des APPAREILS ELECTROMEDICAUX et des SYSTEMES ELECTROMEDICAUX
    61
  • 209 Exigences pour une conception éco-responsable
    62
  • 210 Exigences de PROCESSUS pour le développement des asservissements physiologiques en boucle fermée
    62
  • 211 Exigences applicables aux APPAREILS ELECTROMEDICAUX et aux SYSTEMES ELECTROMEDICAUX utilisés dans l'environnement des soins à domicile
    62
  • ANNEXE C (informative) Guide pour le marquage et exigences d'étiquetage pour les APPAREILS EM et les SYSTEMES EM ou bien leurs parties
    63
  • ANNEXE D (informative) Symboles des marquages
    76
  • ANNEXE AA (informative) Lignes directrices particulières et justifications
    78
  • ANNEXE BB (normative) Essai d'inflammabilité des agents anesthésiques
    96
  • ANNEXE CC (informative) Aspects environnementaux
    97
  • ANNEXE DD (informative) Référence aux principes essentiels
    100
  • Bibliographie
    110
  • Index alphabétique des termes définis utilisés dans la présente Norme particulière
    112
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