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ISO 21856:2022

Current Revision

Assistive products - General requirements and test methods

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This document specifies general requirements and test methods for assistive products, considered to be medical devices, intended for use to alleviate or compensate for a disability.

This document does not apply to assistive products which achieve their intended purpose by administering pharmaceutical substances to the user.

NOTE 1    Assistive products are considered to be medical devices in some jurisdictions but not in others.

NOTE 2    Requirements and test methods for particular types of assistive products are given in other International Standards, e.g. see Reference [33].

NOTE 3    Not all the items listed in ISO 9999 are medical devices. Contracting parties might wish to consider if this document or specific clauses or subclauses can be used for assistive products that are not medical devices.


SDO ISO: International Organization for Standardization
Document Number ISO 21856
Publication Date Not Available
Language en - English
Page Count
Revision Level
Supercedes
Committee ISO/TC 173
Publish Date Document Id Type View
Not Available ISO 21856:2022 Revision