NF EN ISO 5367
Anaesthetic and respiratory equipment - Breathing sets and connectors
This document specifies minimum requirements for breathing sets and breathing tubes intended to be used with anaesthetic breathing systems, ventilator breathing systems, humidifiers or nebulizers. It applies to breathing sets and breathing tubes and patient end adaptors supplied already assembled and to those supplied as components and assembled in accordance with the manufacturer?s instructions.This document is applicable to breathing sets which include special components (e.g. water traps) between the patient end and machine end.Provision is made for coaxial and related bifurcated, double-lumen, or multiple-lumen breathing sets and breathing tubes suitable for use with patient end adaptors.
This document specifies minimum requirements for breathing sets and breathing tubes intended to be used with anaesthetic breathing systems, ventilator breathing systems, humidifiers or nebulizers. It applies to breathing sets and breathing tubes and patient end adaptors supplied already assembled and to those supplied as components and assembled in accordance with the manufacturer?s instructions.
This document is applicable to breathing sets which include special components (e.g. water traps) between the patient end and machine end.
Provision is made for coaxial and related bifurcated, double-lumen, or multiple-lumen breathing sets and breathing tubes suitable for use with patient end adaptors.
ISO 5367:2014 specifies basic requirements for breathing sets and breathing tubes intended to be used with anaesthetic breathing systems, ventilator breathing systems, humidifiers or nebulizers. It applies to breathing sets and breathing tubes and patient end adaptors supplied already assembled and to those supplied as components and assembled in accordance with the manufacturer's instructions. ISO 5367:2014 is applicable to breathing sets which include special components (e.g. water traps) between the patient end and machine end which are supplied already assembled. Provision is made for coaxial and related bifurcated, double-lumen, or multiple-lumen breathing sets and breathing tubes suitable for use with patient end adaptors.
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1 Domaine d'application
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2 Références normatives
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3 Termes et définitions
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4 Exigences générales
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5 Matériaux
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6 Exigences de calcul
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7 Exigences concernant les ensembles respiratoires et les tubes respiratoires fournis à l'état stérile
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8 Emballage
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9 Informations à fournir par le fabricant
- Annexe A (informative) Justifications
- Annexe B (informative) Identification des phénomènes dangereux en vue de la gestion des risques
- Annexe C (normative) Essai concernant la sécurité du raccordement entre une extrémité simple et un raccord conique
- Annexe D (normative) Essai concernant la sécurité du raccordement des extrémités assemblées et la résistance axiale des tubes respiratoires
- Annexe E (normative) Essai concernant les fuites
- Annexe F (normative) Mesurage de la résistance à l'écoulement
- Annexe G (normative) Essai concernant l'augmentation de la résistance à l'écoulement avec la flexion
- Annexe H (normative) Essai de compliance
- Bibliographie
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The identification of these types of clauses is based on the document “ISO / IEC Directives, Part 2 - Principles and rules of structure and drafting of ISO documents ”as well as on a constantly enriched list of verbal forms.
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