ISO 27427:2023

Anaesthetic and respiratory equipment — Nebulizing systems and components

OVERVIEW

This document specifies requirements for the safety and performance testing of general-purpose nebulizing systems intended for continuous or breath-actuated delivery of liquids, in aerosol form, to humans through the respiratory system.

This document includes gas-powered nebulizers (which can be powered by, e.g., compressors, pipeline systems, cylinders, etc.) and electrically powered nebulizers [e.g. spinning disc, ultrasonic, vibrating mesh (active and passive), and capillary devices] or manually powered nebulizers. This document does not specify the electrical requirements of electrically powered nebulizers.

This document does not specify the minimum performance of nebulizing systems.

This document does not apply to:

a)       devices intended for nasal deposition;

b)       devices intended solely to provide humidification or hydration by providing water in aerosol form.

NOTE 1        ISO 80601-2-74 and ISO 20789 cover these devices.

c)        drug-specific nebulizers or their components (e.g. metered dose inhalers, metered liquid inhalers, dry powder inhalers).

NOTE 2        ISO 20072 covers these devices.

NOTE 3        See Annex A for rationale.

COMMENTS

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PRODUCT DETAILS

Status Current
Edition 2023
No. of Pages 33
ICS Classification 11.040.10 Anaesthetic, respiratory and reanimation equipment
Committee ISO/TC 121/SC 2
Available for Purchase For sale in Singapore only
Adoption ISO