STANDARD

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ÖNORM EN ISO 80601-2-79

Issue date: 2025 02 15

Medical electrical equipment - Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment (ISO 80601-2-79:2024)

This document applies to the basic safety and essential performance of ventilatory support equipment for ventilatory impairment, hereafter also referred to as ME equipment, in combination with its accessories: — intended for use in the home healthcare environment; — intended for use by a lay operator; — intended for use with patients who have ventilatory impairment, the most fragile of these patients, would not likely experience injury with the loss of this artificial ventilation; and — not intended for patients who are dependent on artificial ventilation for their immediate life support. Ventilatory support equipment is not considered to use a physiologic closed-loop control system unless it uses a physiological patient variable to adjust the artificial ventilation therapy settings. This document is also applicable to those accessories intended by their manufacturer to be connected to the breathing system of ventilatory support equipment for ventilatory impairment, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilatory support equipment for ventilatory impairment. If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems 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 ME equipment and to ME systems, as relevant. Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1. This document does not specify the requirements for: — ventilators or accessories for ventilator-dependent patients intended for critical care applications, which are given in ISO 80601-2-12; — ventilators or accessories intended for anaesthetic applications, which are given in ISO 80601-2-13; — ventilators or accessories intended for the emergency medical services environment, which are given in ISO 80601-2-84; — ventilators or accessories intended for ventilator-dependent patients in the home healthcare environment, which are given in ISO 80601-2-72; — ventilatory support equipment or accessories intended for ventilatory insufficiency, which are given in ISO 80601-2-80; — sleep apnoea therapy ME equipment, which are given in ISO 80601-2-70; — high-frequency jet ventilators (HFJVs), which are given in ISO 80601-2-87; — high-frequency oscillatory ventilators (HFOVs); — respiratory high flow equipment, which are given in ISO 80601-2-90; — user-powered resuscitators, which are given in ISO 10651-4; — gas-powered emergency resuscitators, which are given in ISO 10651-5; — oxygen therapy constant flow ME equipment; — cuirass or “iron-lung” ventilation equipment.

General information on ÖNORM EN ISO 80601-2-79

Format
Paper | 128 Pages
Language
German | English | Download GER/ENG
Publisher
Austrian Standards International

Timeline

An overview of the development of ÖNORM EN ISO 80601-2-79 from 2004 til today.

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Normative References

Here you will find an extract of the normative references. Please refer to the document itself for the full list.

Dokumentnummer Titel Ausgabedatum Art Link
Dokumentnummer
ISO 14937:2009
Titel
Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Ausgabedatum
2009 10 14
Art
Standard
Dokumentnummer
ISO 17664-1:2021
Titel
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
Ausgabedatum
2021 07 06
Art
Standard
Dokumentnummer
ISO 17664-2:2021
Titel
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
Ausgabedatum
2021 02 25
Art
Standard
Dokumentnummer
ISO 18562-1:2024
Titel
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
Ausgabedatum
2024 03 08
Art
Standard
Dokumentnummer
ISO 20417:2021
Titel
Medical devices — Information to be supplied by the manufacturer (Corrected version 2021-12)
Ausgabedatum
2021 04 13
Art
Standard
Dokumentnummer
ISO 23328-1:2003
Titel
Breathing system filters for anaesthetic and respiratory use — Part 1: Salt test method to assess filtration performance
Ausgabedatum
2003 08 20
Art
Standard
Dokumentnummer
ISO 23328-2:2002
Titel
Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects
Ausgabedatum
2002 10 22
Art
Standard
Dokumentnummer
ISO 3744:2010
Titel
Acoustics — Determination of sound power levels and sound energy levels of noise sources using sound pressure — Engineering methods for an essentially free field over a reflecting plane
Ausgabedatum
2010 09 22
Art
Standard
Dokumentnummer
ISO 4871:1996
Titel
Acoustics — Declaration and verification of noise emission values of machinery and equipment
Ausgabedatum
1996 12 19
Art
Standard
Dokumentnummer
ISO 5356-1:2015
Titel
Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets
Ausgabedatum
2015 03 13
Art
Standard
Dokumentnummer
ISO 5367:2023
Titel
Anaesthetic and respiratory equipment — Breathing sets and connectors
Ausgabedatum
2023 07 14
Art
Standard
Dokumentnummer
ISO 7396-1:2016
Titel
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum
Ausgabedatum
2016 02 15
Art
Standard
Dokumentnummer
ISO 80369-1:2018
Titel
Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements
Ausgabedatum
2018 11 05
Art
Standard
Dokumentnummer
ISO 80601-2-74:2021
Titel
Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
Ausgabedatum
2021 07 13
Art
Standard
Dokumentnummer
ISO 9360-1:2000
Titel
Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 1: HMEs for use with minimum tidal volumes of 250 ml
Ausgabedatum
2000 03 16
Art
Standard
Dokumentnummer
ISO 9360-2:2001
Titel
Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml
Ausgabedatum
2001 05 10
Art
Standard

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