NF EN ISO 10524-3
Pressure regulators for use with medical gases - Part 3 : pressure regulators integrated with cylinder valves (VIPRs)
This document specifies design, type testing, and marking requirements for cylinder valves with integrated pressure regulators [as defined in 3.26 and referred to hereafter as valves with integrated pressure regulators (VIPRs)] intended for the administration of medical gases in the treatment, management, diagnostic evaluation and care of patients or for gases used for driving surgical tools. Examples of gases include oxygen, medical air and oxygen/nitrous oxide mixtures. This document applies to VIPRs mounted on refillable cylinders with a working pressure up to 30 000 kPa (300 bar) intended to be filled in cylinder filling facilities or on self-filling systems as used in homecare applications. VIPRs covered by this document are pressure pre-set and provided with a pressure outlet and/or pre-set flow outlet(s).
This document specifies design, type testing, and marking requirements for cylinder valves with integrated pressure regulators [as defined in 3.26 and referred to hereafter as valves with integrated pressure regulators (VIPRs)] intended for the administration of medical gases in the treatment, management, diagnostic evaluation and care of patients or for gases used for driving surgical tools.
Examples of gases include oxygen, medical air and oxygen/nitrous oxide mixtures.
This document applies to VIPRs mounted on refillable cylinders with a working pressure up to 30 000 kPa (300 bar) intended to be filled in cylinder filling facilities or on self-filling systems as used in homecare applications.
VIPRs covered by this document are pressure pre-set and provided with a pressure outlet and/or pre-set flow outlet(s).
Le présent document fixe les exigences et essais des détendeurs dans les robinets de gaz médicaux. Ces détendeurs peuvent être équipés de dispositifs de régulation et de mesure de débit.
Le présent document est l'amendement 1 à la norme homologuée NF EN ISO 10524-3 de juillet 2006. Il modifie les paragraphes 5.4.9 et 8.1.
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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 Nomenclature
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5 Exigences générales
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6 Exigences relatives à la conception
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7 Exigences relatives à la construction
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8 Méthodes d'essai pour les essais de type non spécifiques au gaz
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9 * Essais de type spécifiques au gaz
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10 Marquage, code couleur et emballage
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11 * Informations devant être fournies par le fabricant
- Annexe A Exemples de VIPR
- Annexe B Justificatif
- Annexe C Écarts régionaux et nationaux en matière de code couleur et de nomenclature des gaz médicaux
- Bibliographie
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