NF EN ISO 5367

NF EN ISO 5367

November 2014
Standard Cancelled

Anaesthetic and respiratory equipment - Breathing sets and connectors

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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Main informations

Collections

National standards and national normative documents

Publication date

November 2014

Number of pages

45 p.

Reference

NF EN ISO 5367

ICS Codes

11.040.10   Anaesthetic, respiratory and reanimation equipment

Classification index

S95-135

Print number

1

International kinship

European kinship

EN ISO 5367:2014
Sumary
Anaesthetic and respiratory equipment - Breathing sets and connectors

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.

Replaced standards (1)
NF EN 12342+A1
November 2009
Standard Cancelled
Breathing tubes intended for use with anaesthetic apparatus and ventilators.

Le présent document spécifie les prescriptions des tubes respiratoires utilisés avec des appareils d'anesthésie et la plupart des ventilateurs, humidificateurs et nébuliseurs. Il définit également les matériaux, la conception, la longueur, la résistance à l'écoulement, les moyens de raccordement, l'étanchéité, l'augmentation de la résistance à l'écoulement sous flexion, la compliance des tubes respiratoires, les informations fournies par le fabricant, la résistance électrique, les exigences relatives aux tubes respiratoires fournis stériles ainsi que le marquage. Le présent document vient à l'appui des exigences essentielles de la Directive UE 93/42/CEE sur les dispositifs médicaux.

Standard replaced by (1)
NF EN ISO 5367
July 2023
Standard Current
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.

Table of contents
  • Avant-propos
    iv
  • Introduction
    vi
  • 1 Domaine d'application
    1
  • 2 Références normatives
    1
  • 3 Termes et définitions
    2
  • 4 Exigences générales
    4
  • 5 Exigences particulières
    5
  • 6 Prévention des charges électrostatiques
    9
  • 7 Exigences concernant les systèmes respiratoires et les tubes respiratoires fournis à l'état stérile
    10
  • 8 Marquage
    10
  • Annexe A (informative) Justifications
    14
  • Annexe B (informative) Identification des dangers pour l'appréciation des risques
    24
  • Annexe C (normative) Essai concernant la sécurité du raccordement entre une extrémité simple et un raccord conique
    25
  • Annexe D (normative) Essai concernant la sécurité du raccordement entre l'adaptateur et le tube respiratoire
    26
  • Annexe E (normative) Essai concernant les fuites
    27
  • Annexe F (normative) Mesurage de la résistance à l'écoulement
    29
  • Annexe G (normative) Essai concernant l'augmentation de la résistance à l'écoulement avec la flexion
    32
  • Annexe H (normative) Essai concernant la compliance
    34
  • Bibliographie
    36
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