NF EN ISO 80601-2-13
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.
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.
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.
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.
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.
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.
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.
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.
- Avant-proposv
- Introductionvi
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201.1 Domaine d'application, objet et normes connexes1
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201.2 Références normatives3
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201.3 Termes et définitions5
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201.4 Exigences générales10
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201.5 Exigences générales relatives aux essais des APPAREILS EM12
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201.6 Classification des APPAREILS EM et des SYSTEMES EM13
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201.7 Identification, marquage et documentation des APPAREILS EM13
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201.8 Protection contre des DANGERS d'origine électrique provenant des APPAREILS EM17
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201.9 Protection contre les DANGERS mécaniques des APPAREILS EM et des SYSTEMES EM18
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201.10 Protection contre des DANGERS dus aux rayonnements involontaires et excessifs19
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201.11 Protection contre les températures excessives et les autres DANGERS19
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201.12 Précision des commandes, des instruments et protection contre les caractéristiques de sortie présentant des risques22
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201.13 SITUATIONS DANGEREUSES et conditions de défaut27
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201.14 SYSTEMES ELECTROMEDICAUX PROGRAMMABLES (SEMP)28
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201.15 Construction de l'APPAREIL EM28
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201.16 SYSTEMES EM28
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201.17 Compatibilité électromagnétique des APPAREILS EM et des SYSTEMES EM29
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201.101 Exigences supplémentaires applicables aux SYSTEMES D'ADMINISTRATION DE GAZ ANESTHESIQUE29
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201.102 Exigences supplémentaires applicables à un SYSTEME D'ANESTHESIE PAR VOIE RESPIRATOIRE35
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201.103 Exigences supplémentaires applicables à une SYSTEME D'EVACUATION DES GAZ ANESTHESIQUES44
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201.104 Exigences supplémentaires applicables à un SYSTEME D'ADMINISTRATION DE VAPEUR ANESTHESIQUE48
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201.105 Exigences supplémentaires applicables à un ventilateur d'anesthesie53
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201.106 Boucles d'affichage59
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201.107 Évaluation clinique60
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202 Compatibilité électromagnétique - Exigences et essais60
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203 Exigences générales applicables à une radioprotection dans les appareils à rayonnement X de diagnostic60
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206 Aptitude à l'utilisation60
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208 Exigences générales, essais et guide pour les SYSTEMES D'ALARME des APPAREILS ELECTROMEDICAUX et des SYSTEMES ELECTROMEDICAUX61
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209 Exigences pour une conception éco-responsable62
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210 Exigences de PROCESSUS pour le développement des asservissements physiologiques en boucle fermée62
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211 Exigences applicables aux APPAREILS ELECTROMEDICAUX et aux SYSTEMES ELECTROMEDICAUX utilisés dans l'environnement des soins à domicile62
- ANNEXE C (informative) Guide pour le marquage et exigences d'étiquetage pour les APPAREILS EM et les SYSTEMES EM ou bien leurs parties63
- ANNEXE D (informative) Symboles des marquages76
- ANNEXE AA (informative) Lignes directrices particulières et justifications78
- ANNEXE BB (normative) Essai d'inflammabilité des agents anesthésiques96
- ANNEXE CC (informative) Aspects environnementaux97
- ANNEXE DD (informative) Référence aux principes essentiels100
- Bibliographie110
- Index alphabétique des termes définis utilisés dans la présente Norme particulière112
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