NF EN ISO 17510-1

NF EN ISO 17510-1

July 2009
Standard Cancelled

Sleep apnoea breathing therapy - Part 1 : sleep apnoea breathing therapy equipment

ISO 17510-1:2007 specifies requirements for equipment intended for sleep apnoea breathing therapy for domiciliary use, ships, aircraft and other transport vehicles and for use in healthcare institutions. ISO 17510-1:2007 applies to equipment intended for use with adults and children, and excludes equipment intended for use with neonates. Jet and very high frequency ventilation and oscillation are not considered in ISO 17510-1:2007.

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Collections

National standards and national normative documents

Publication date

July 2009

Number of pages

51 p.

Reference

NF EN ISO 17510-1

ICS Codes

11.040.10   Anaesthetic, respiratory and reanimation equipment
11.040.60   Therapy equipment

Classification index

S95-182-1

Print number

1 - 18/06/2009

International kinship

European kinship

EN ISO 17510-1:2009
Sumary
Sleep apnoea breathing therapy - Part 1 : sleep apnoea breathing therapy equipment

ISO 17510-1:2007 specifies requirements for equipment intended for sleep apnoea breathing therapy for domiciliary use, ships, aircraft and other transport vehicles and for use in healthcare institutions.

ISO 17510-1:2007 applies to equipment intended for use with adults and children, and excludes equipment intended for use with neonates.

Jet and very high frequency ventilation and oscillation are not considered in ISO 17510-1:2007.

Replaced standards (1)
NF EN ISO 17510-1
November 2007
Standard Cancelled
Sleep apnoea breathing therapy - Part 1 : sleep apnoea breathing therapy equipment

Le présent document spécifie les exigences relatives aux équipements destinés à la thérapie respiratoire de l'apnée du sommeil pour un usage à domicile , en transport ainsi que dans les établissements hospitaliers. Il s'applique aux équipements destinés aux adultes et aux enfants, à l'exclusion des équipements destinés aux nouveaux-nés. Le présent document est une norme harmonisée entrant dans le cadre de la Directive UE 93/42/CEE. La partie 2 traite des masques et accessoires.

Standard replaced by (1)
NF EN ISO 80601-2-70
November 2020
Standard Current
Medical electrical equipment - Part 2-70 : particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment

<p>This document is applicable to the <i>basic safety</i> and <i>essential performance</i> of <i>sleep apnoea breathing therapy equipment</i>, hereafter referred to as <i>ME equipment, </i>intended to alleviate the symptoms of <i>patients</i> who suffer from obstructive sleep apnoea by delivering a therapeutic breathing pressure to the respiratory tract of the <i>patient.</i> <i>Sleep apnoea breathing therapy equipment</i> is intended for use in the <i>home healthcare environment</i> by <i>lay operators</i> as well as in professional healthcare institutions.</p> <p>* <i>Sleep apnoea breathing therapy equipment</i> is not considered to utilize a <i>physiologic closed-loop-control system</i> unless it uses a physiological <i>patient</i> variable to adjust the therapy settings.</p> <p>This document excludes <i>sleep apnoea breathing therapy equipment</i> intended for use with neonates.</p> <p>This document is applicable to <i>ME equipment</i> or an <i>ME system</i> intended for those <i>patients</i> who are not dependent on mechanical ventilation. </p> <p>This document is not applicable to <i>ME equipment</i> or an <i>ME system</i> intended for those <i>patients</i> who are dependent on mechanical ventilation such as <i>patients</i> with central sleep apnoea. </p> <p>This document is also applicable to those <i>accessories</i> intended by their <i>manufacturer</i> to be connected to <i>sleep apnoea breathing therapy equipment</i>, where the characteristics of those <i>accessories</i> can affect the <i>basic safety</i> or <i>essential performance</i> of the <i>sleep apnoea breathing therapy equipment</i>. </p> <p><i>Masks</i> and application <i>accessories</i> intended for use during sleep apnoea breathing therapy<i> </i>are additionally addressed by ISO 17510. Refer to Figure AA.1 for items covered further under this document. </p> <p>If a clause or subclause is specifically intended to be applicable to <i>ME equipment</i> only, or to <i>ME systems</i> only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to <i>ME equipment</i> and to <i>ME systems</i>, as relevant.</p> <p><i>Hazards</i> inherent in the intended physiological function of <i>ME equipment</i> or <i>ME systems</i> within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of the general standard.</p> <p>NOTE See also 4.2 of the general standard.</p> <p>This document is not applicable to high-frequency jet ventilators (HFJVs) or high-frequency oscillatory ventilators (HFOVs), which are given in ISO 80601-2-87<sup>[13]</sup>.</p> <p>This document does not specify the requirements for ventilators or <i>accessories</i> intended for critical care ventilators for ventilator-dependent <i>patients,</i> which are given in ISO 80601‑2‑12.</p> <p>This document does not specify the requirements for ventilators or <i>accessories</i> intended for anaesthetic applications, which are given in ISO 80601-2-13<sup>[8]</sup>.</p> <p>This document does not specify the requirements for ventilators or <i>accessories</i> intended for home care ventilators for ventilator-dependent <i>patients,</i> which are given in ISO 80601-2-72<sup>[9]</sup>.</p> <p>This document does not specify the requirements for ventilators or <i>accessories</i> intended for emergency and transport, which are given in ISO 80601-2-84<sup>[12]</sup>.</p> <p>This document does not specify the requirements for ventilators or <i>accessories</i> intended for home-care ventilatory support, which are given in ISO 80601-2-79<sup>[10]</sup> and ISO 80601‑2‑80<sup>[11]</sup>. </p>

Table of contents
View the extract
  • Avant-propos
    v
  • Introduction
    vi
  • 1 Domaine d'application
    1
  • 2 Références normatives
    2
  • 3 Termes et définitions
    3
  • 4 Exigences
    4
  • 5 Classification et désignation
    4
  • 6 Marquage, étiquetage et emballage
    4
  • 7 Puissance absorbée
    8
  • 8 Catégories fondamentales de sécurité
    8
  • 9 Moyens de protection amovibles
    8
  • 10 Conditions d'environnement
    8
  • 11 Non utilisé
    9
  • 12 Non utilisé
    9
  • 13 Généralités
    9
  • 14 Exigences relatives à la classification
    9
  • 15 Limitation de la tension et/ou de l'énergie
    10
  • 16 Enveloppes et capots de protection
    10
  • 17 Séparation
    10
  • 18 Mise à la terre de protection, mise à la terre fonctionnelle et égalisation des potentiels
    10
  • 19 Courants de fuite permanents et courant auxiliaire patient
    10
  • 20 Tension de tenue
    10
  • 21 Résistance mécanique
    10
  • 22 Parties en mouvement
    10
  • 23 Surfaces, angles et arêtes
    10
  • 24 Stabilité en utilisation normale
    11
  • 25 Projection d'objets
    11
  • 26 Vibrations et bruit
    11
  • 27 Puissance pneumatique et puissance hydraulique
    12
  • 28 Masses suspendues
    12
  • 29 Rayonnements X
    12
  • 30 Rayonnements alpha, bêta, gamma, neutroniques et d'autres particules
    12
  • 31 Rayonnements à micro-ondes
    12
  • 32 Rayonnements lumineux (y compris les rayonnements lasers)
    12
  • 33 Rayonnements infrarouges
    12
  • 34 Rayonnements ultraviolets
    12
  • 35 Énergie acoustique (y compris les ultrasons)
    12
  • 36 Compatibilité électromagnétique
    13
  • 37 Localisations et exigences fondamentales
    13
  • 38 Marquage et documents d'accompagnement
    13
  • 39 Exigences communes aux appareils de la catégorie AP et de la catégorie APG
    13
  • 40 Exigences et essais pour les appareils de la catégorie AP, parties et composants de ceux-ci
    13
  • 41 Exigences et essais pour les appareils de la catégorie APG, parties et composants de ceux-ci
    13
  • 42 Températures excessives
    13
  • 43 Prévention du feu
    14
  • 44 Débordements, renversements, fuites, humidité, pénétration de liquides, nettoyage, stérilisation et désinfection
    14
  • 45 Réservoirs et parties sous pression
    15
  • 46 Erreurs humaines
    15
  • 47 Charges électrostatiques
    15
  • 48 Biocompatibilité
    15
  • 49 Coupure de l'alimentation électrique
    16
  • 50 Précision des caractéristiques de fonctionnement
    16
  • 51 Protection contre les caractéristiques de sortie présentant des risques
    16
  • 52 Fonctionnement anormal et conditions de défauts
    17
  • 53 Essais d'environnement
    17
  • 54 Généralités
    17
  • 55 Enveloppes et capots
    18
  • 56 Composants et ensembles
    18
  • 57 Parties reliées au réseau, composants et montage
    20
  • 58 Mise à la terre de protection - Bornes et raccordements
    20
  • 59 Construction et montage
    20
  • Annexe AA (informative) Exposé des motifs
    21
  • Annexe BB (normative) Méthodes d'essai portant sur l'exactitude de la pression en utilisation normale
    27
  • Annexe CC (normative) Méthode d'essai du débit maximal
    30
  • Annexe DD (informative) Aspects environnementaux
    31
  • Annexe EE (informative) Référence aux principes essentiels
    33
  • Annexe FF (informative) Terminologie - Index alphabétique des termes définis
    35
  • Bibliographie
    37
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