NF EN 13328-2

NF EN 13328-2

January 2003
Standard Cancelled

Breathing system filters for anaesthetic and respiratory use - Part 2 : non-filtration aspects

Le présent document spécifie les exigences s'appliquant aux aspects autres que la filtration des filtres pour systèmes respiratoires destinés à filtrer les gaz respirés par les êtres humains. Il traite des orifices de raccordement, des fuites, de la résistance au débit, de l'emballage, du marquage et des informations fournies.

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Main informations

Collections

National standards and national normative documents

Publication date

January 2003

Number of pages

10 p.

Reference

NF EN 13328-2

ICS Codes

11.040.10   Anaesthetic, respiratory and reanimation equipment

Classification index

S95-172-2

Print number

1 - 22/01/2003

European kinship

EN 13328-2:2002
Sumary
Breathing system filters for anaesthetic and respiratory use - Part 2 : non-filtration aspects

Le présent document spécifie les exigences s'appliquant aux aspects autres que la filtration des filtres pour systèmes respiratoires destinés à filtrer les gaz respirés par les êtres humains. Il traite des orifices de raccordement, des fuites, de la résistance au débit, de l'emballage, du marquage et des informations fournies.
Standard replaced by (1)
NF EN ISO 23328-2
August 2008
Standard Cancelled
Breathing system filters for anaesthetic and respiratory use - Part 2 : non-filtration aspects

ISO 23328-2:2002 specifies requirements for non-filtration aspects of breathing system filters (BSF) intended for anaesthetic and respiratory use, and addresses connection ports, leakage, resistance to flow, packaging, marking and information supplied. The test method is intended for BSF used with a clinical breathing system. It is not applicable to other types of filter, e.g. those designed to protect vacuum sources or gas sample lines, to filter compressed gases, or to protect test equipment for physiological respiratory measurements. A method for assessing filtration performance of BSF is given in ISO 23328-1.

Table of contents
  • Avant-propos
    3
  • 1 Domaine d'application
    3
  • 2 Références normatives
    3
  • 3 Termes et définitions
    4
  • 4 Raccords d'orifices de filtre pour système respiratoire
    4
  • 4.1 Système respiratoire et orifices de raccordement côté patient
    4
  • 4.2 Orifices accessoires
    4
  • 5 Méthodes d'essai
    5
  • 5.1 Conditions d'essai
    5
  • 5.2 Mesurage de la chute de pression
    5
  • 5.3 Méthode d'essai de résistance aux fuites de gaz
    5
  • 6 Exigences relatives aux filtres pour système respiratoire fournis stériles
    5
  • 6.1 Assurance de stérilité
    5
  • 6.2 Emballage des filtres fournis stériles
    5
  • 7 Marquage
    5
  • 7.1 Utilisation de symboles
    5
  • 7.2 Marquage du filtre pour système respiratoire
    6
  • 7.3 Marquage de l'emballage
    6
  • 7.4 Filtres non réutilisables
    6
  • 8 Informations à fournir par le fabricant
    6
  • Annexe ZA (informative)Articles de la présente norme européenne concernant les exigences essentielles ou d'autres dispositions des Directives UE
    7
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