ISO 20417:2021

Medical devices — Information to be supplied by the manufacturer ISO 20417:2021

General information

90.92 Standard to be revised   Dec 18, 2023

ISO

ISO/TC 210 Quality management and corresponding general aspects for medical devices

International Standard

11.040.01   Medical equipment in general

Scope

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.

Life cycle

NOW

PUBLISHED
ISO 20417:2021
90.92 Standard to be revised
Dec 18, 2023

REVISED BY

IN_DEVELOPMENT
ISO/CD 20417