ISO 20417:2021现行

NOTE1 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.NOTE2 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.

?VE/?NORM EN ISO 20417:2021 11 15 - Identical

PN-EN ISO 20417:2021 - Identical

UNI CEI EN ISO 20417:2021 - Identical

?VE/?NORM EN ISO 20417:2022 09 01 - Identical

SN EN ISO 20417:2021 - Identical

NF EN ISO 20417:2021 - Identical

SS-ISO 20417:2021 - Identical

I.S. EN ISO 20417:2021 - Identical

EN ISO 20417:2021 - Identical

I.S. EN ISO 20417:2021&LC:2021 - Identical

BS EN ISO 20417:2021 - Identical

BS EN ISO 20417:2021 - Identical

UNE-EN ISO 20417:2021 - Identical