STANDARD

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ÖNORM EN ISO 10651-4

Issue date: 2023 10 15

Lung ventilators - Part 4: Particular requirements for user-powered resuscitators (ISO 10651-4:2023)

This document specifies requirements for user-powered resuscitators intended for use with all age groups and which are intended to provide lung ventilation to patients whose breathing is inadequate. User-powered resuscitators are designated according to ideal body mass range. Example user-powered resuscitators include: - self-inflating bag resuscitators intended to be squeezed by the user’s hand and refilled by elastic recoil; and - flow-inflating bag resuscitators intended to be squeezed by the user’s hand and refilled by a flow from a medical gas source. This document is also applicable to those accessories that are intended for use with resuscitators where the characteristics of those accessories can affect the safety of the user-powered resuscitator. Examples of such accessories include face masks, PEEP valves, capnometric indicators, manometers, metronomes, flow restrictors, filters, gas refill valves, oxygen gas mixers, connectors, electronic feedback devices, electronic sensors and transmission of data to other equipment. This document is also applicable to point-of-use packaging. This document does not specify the requirements for: - gas-powered emergency resuscitators, which are given in ISO 10651-5; - electrically-powered resuscitators; - gas powered resuscitators for professional healthcare facilities; and - anaesthetic reservoir bags, which are given in ISO 5362.

General information on ÖNORM EN ISO 10651-4

Format
Digital | 88 Pages
Language
German | English | Download GER/ENG
Publisher
Austrian Standards International

Timeline

An overview of the development of ÖNORM EN ISO 10651-4 from 2002 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 10993-1:2018
Titel
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process (Corrected version 2018-10)
Ausgabedatum
2018 08 17
Art
Standard
Dokumentnummer
ISO 11195:2018
Titel
Gas mixers for medical use — Stand-alone gas mixers
Ausgabedatum
2018 01 25
Art
Standard
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 14971:2019
Titel
Medical devices — Application of risk management to medical devices
Ausgabedatum
2019 12 10
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 18562-1:2017
Titel
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
Ausgabedatum
2017 03 13
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 23328-2:2002
Titel
Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects
Ausgabedatum
2002 10 22
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

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