
ISO 27427:2023
ISO 27427:2023 Anaesthetic and respiratory equipment – Nebulizing systems and components
CDN $273.00
Description
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.
Edition
4
Published Date
2023-07-14
Status
PUBLISHED
Pages
33
Format 
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment
Abstract
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.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-

ISO 80601:2024 Medical electrical equipment – Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
CDN $390.00 Add to cart -

ISO 18562:2024 Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 1: Evaluation and testing within a risk management process
CDN $273.00 Add to cart -

ISO 32:1977 Gas cylinders for medical use – Marking for identification of content
CDN $76.00 Add to cart -

ISO 16571:2024 Systems for evacuation of plume generated by medical devices
CDN $312.00 Add to cart







