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.

This first edition of ISO 21856 cancels and replaces ISO 16201:2006, which has been technically revised. The main changes compared to the previous edition are as follows: — scope changed to requirements and test methods for assistive products in general.

This first edition of ISO 21856 cancels and replaces ISO 16201:2006, which has been technically revised. The main changes compared to the previous edition are as follows:? scope changed to requirements and test methods for assistive products in general.

I.S. EN ISO 21856:2022 V1.00 is the version of the NSAI adopted European document EN ISO 21856:2022, Assistive products - General requirements and test methods (ISO 21856:2022), including any Corrections, Amendments etc. to EN ISO 21856:2022. This normative document by CEN/CENELEC the elaboration of which includes a public enquiry, followed

This first edition of ISO 21856 cancels and replaces ISO 16201:2006, which has been technically revised. The main changes compared to the previous edition are as follows: — scope changed to requirements and test methods for assistive products in general.

Jul 25, 2022 · Assistive products – General requirements and test methods (ISO 21856:2022) 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.

ISO 21856 was prepared by ISO/TC 173, Assistive Products for persons with disability which is in line with EN 12182 Assistive Products for persons with disability - General Requirements and Test methods. This document supersedes ISO 16201 (E).

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.

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.