Standard

ISO 21856:2022

Jul 2022 Current

Existing or new amendments and versions must be purchased separately.

Language English French

Services Online + Pdf CHF 204,00 Online CHF 175,00

There are no extended editions available for this standard

There are no available corrigendum or amendments for this standard. Any future corrigendum and amendments will be added automatically for subscribers.

Abstract

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.

Products specifications

Standard from ISO
Published: July 4 2022
Edition: 1
Document type: IS
Pages
ISBN:

Publisher: ISO
Distributor: ISO
ICS: 11.180.01
International TC: ISO/TC 173

Product Relations

Adopted by: NF EN ISO 21856:2022
Revises: ISO 16201:2006

ISO 21856:2022

Create subscription

ISO 21856:2022

ISO 16201:2006

Abstract

Products specifications

Product Relations

Product life cycle

Extended editions Extended editions (0)

Version history Related Corrigenda and Amendments (0)

Version history History (2)

ISO 21856:2022

ISO 16201:2006

Abstract

Products specifications

Product Relations

Product life cycle