ISO 80601-2-69:2026

Medical electrical equipment Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment (Edition 3, 2026)

Medical electrical equipment Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment (Edition 3, 2026)

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Referenced standards

IEC 61672-1:2013IEC 62443-4-2:2019IEC 62570:2014IEC 81001-5-1:2021IEC Guide 115:2023ISO 14937:2009ISO 14971:2019ISO 15223-1:2021ISO 16142-1:2016ISO 17256:2024ISO 17664-1:2021ISO 17664-2:2021ISO 18562-1:2024ISO 19223:2019ISO 20417:2026ISO 3744:2010ISO 4135:2022ISO 4871:1996ISO 9000:2015
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ISO 80601-2-69:2026

Medical electrical equipment Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment (Edition 3, 2026)

Medical electrical equipment Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment (Edition 3, 2026)

Abstract
This document is applicable to a transit-operable and non-transit-operable oxygen concentrator. This document is applicable to an oxygen concentrator integrated into or used with other medical devices, ME equipment or ME systems.

EXAMPLE 1 An oxygen concentrator with integrated oxygen conserving equipment function or humidifier function.

EXAMPLE 2 An oxygen concentrator used with a flowmeter stand.

EXAMPLE 3 An oxygen concentrator as part of an anaesthetic system for use in areas with limited logistical supplies of electricity and anaesthetic gases[2].

EXAMPLE 4 An oxygen concentrator with an integrated liquid reservoir function or gas cylinder filling system function.

This document is also applicable to those accessories intended by their manufacturer to be connected to an oxygen concentrator, where the characteristics of those accessories can affect the basic safety or essential performance of the oxygen concentrator.

NOTE 2 Such accessories can include, but are not limited to, masks, cannulae, extension tubing, humidifiers, carts, carrying cases, external power sources and oxygen conserving equipment.

This document does not specify requirements for oxygen concentrators for use with a medical gas pipeline system.

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 7.2.13 and 8.4.1 of the general standard.

NOTE 3 See also 4.2 of the general standard.

General information
Status : Published
Publication date : 2026-04
Stage : International Standard published
Edition : 3
Number of pages : 68