prEN ISO 20417 rev

Medical devices - Information to be supplied by the manufacturer prEN ISO 20417 rev

General information

10.99 New project approved   Dec 19, 2023


CEN/CLC/JTC 3 Quality management and corresponding general aspects for medical devices

European Norm


NOTE 1        There is guidance or rationale for this Clause contained in Clause A.2.
This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging, marking of a medical device or accessory, and accompanying information. This document does not specify the means by which the information is to be supplied.
NOTE 2        Some authorities having jurisdiction impose different requirements for the identification, marking and documentation of a medical device or accessory.
Specific requirements of medical device product standards or group standards take precedence over requirements of this document.

Related legislation

Legislation related to this standard


Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Life cycle


EN ISO 20417:2021


prEN ISO 20417 rev
10.99 New project approved
Dec 19, 2023