NF EN ISO 10524-2

NF EN ISO 10524-2

July 2006
Standard Cancelled

Pressure regulators for use with medical gases - Part 2 : manifold and line pressure regulators

ISO 10524-2:2005 specifies requirements for manifold pressure regulators intended to be connected to cylinders with nominal filling pressures up to 25 000 kPa at 15 °C and for line pressure regulators for inlet pressures up to 3 000 kPa and intended for use in pipeline systems for the following medical gases:oxygen; nitrous oxide; air for breathing; carbon dioxide; oxygen/nitrous oxide mixtures; air for driving surgical tools; nitrogen for driving surgical tools; oxygen produced by an oxygen concentrator.ISO 10524-2:2005 applies to manifold pressure regulators and line pressure regulators supplied as individual units or to the relevant components incorporated within an assembly. It does not apply to pressure regulators for use with vacuum pipeline systems.

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Main informations

Collections

National standards and national normative documents

Publication date

July 2006

Number of pages

41 p.

Reference

NF EN ISO 10524-2

ICS Codes

11.040.10   Anaesthetic, respiratory and reanimation equipment
23.060.40   Pressure regulators

Classification index

S95-159-2

Print number

1 - 07/06/2006

International kinship

European kinship

EN ISO 10524-2:2006
Sumary
Pressure regulators for use with medical gases - Part 2 : manifold and line pressure regulators

ISO 10524-2:2005 specifies requirements for manifold pressure regulators intended to be connected to cylinders with nominal filling pressures up to 25 000 kPa at 15 °C and for line pressure regulators for inlet pressures up to 3 000 kPa and intended for use in pipeline systems for the following medical gases:

oxygen; nitrous oxide; air for breathing; carbon dioxide; oxygen/nitrous oxide mixtures; air for driving surgical tools; nitrogen for driving surgical tools; oxygen produced by an oxygen concentrator.

ISO 10524-2:2005 applies to manifold pressure regulators and line pressure regulators supplied as individual units or to the relevant components incorporated within an assembly. It does not apply to pressure regulators for use with vacuum pipeline systems.

Replaced standards (1)
NF EN 738-2
January 1999
Standard Cancelled
Pressure regulators for use with medical gases. Part 2 : manifold and line pressure regulators.

Le présent document fait partie d'une série de normes sur les détendeurs médicaux. Il fixe toutes les caractéristiques et les essais associés des détendeurs de rampes de bouteilles (à 200 bar) abaissant la pression jusqu'au niveau du réseau primaire (10 bar en France) de canalisation de gaz médicaux.

Standard replaced by (1)
NF EN ISO 10524-2
January 2019
Standard Current
Pressure regulators for use with medical gases - Part 2 : manifold and line pressure regulators

ISO 10524-2:2018 specifies design, construction, type testing, and marking requirements for manifold pressure regulators (as defined in 3.7) and line pressure regulators (as defined in 3.5) intended for use in medical gas pipeline systems. Examples of gases include oxygen, medical air and oxygen/nitrous oxide mixtures. ISO 10524-2:2018 applies to manifold pressure regulators and line pressure regulators supplied as individual units or to the relevant components incorporated within an assembly. Manifold pressure regulators are intended to be connected to a manifold system which has a nominal inlet pressure, P1 of up to 30 000 kPa (300 bar). Line pressure regulators are intended to be connected downstream of the manifold pressure regulator with a supply pressure up to 3 000 kPa (30 bar). ISO 10524-2:2018 does not apply to pressure regulators for use with vacuum pipeline systems. NOTE Requirements for pressure regulators for use with vacuum pipeline systems are covered in ISO 10079‑3.

Table of contents
  • Avant-propos
    iv
  • Introduction
    v
  • 1 Domaine d'application
    1
  • 2 Références normatives
    1
  • 3 Termes et définitions
    2
  • 4 Symboles
    4
  • 5 Exigences générales
    4
  • 5.1 Sécurité
    4
  • 5.2 Autre construction
    4
  • 5.3 Matériaux
    4
  • 5.4 Exigences relatives à la conception
    5
  • 5.5 Exigences relatives à la construction
    9
  • 6 Méthodes d'essai
    9
  • 6.1 Conditions
    9
  • 6.2 Méthodes d'essai des détendeurs de rampes
    10
  • 6.3 Méthodes d'essai des détendeurs de canalisations
    16
  • 6.4 Méthode d'essai pour la détermination de la température d'auto-inflammation des matériaux d'étanchéité et des lubrifiants
    18
  • 6.5 Méthode d'essai pour la durabilité du marquage et du code couleur
    19
  • 7 Marquage, code couleur et emballage
    20
  • 7.1 Marquage
    20
  • 7.2 Code couleur
    22
  • 7.3 Emballage
    22
  • 8 Informations à fournir par le fabricant
    22
  • Annexe A (informative) Exemples de détendeurs
    23
  • Annexe B (informative) Justificatif
    25
  • Annexe C (informative) Écarts régionaux et nationaux en matière de code couleur et de nomenclature pour les gaz médicaux
    27
  • Bibliographie
    29
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