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ISO 15223-1:2021/Amd 1:2025

Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific

General information

Valid from 03.03.2025
Directives or regulations
None

Standard history

Status
Date
Type
Name
03.03.2025
Amendment
06.07.2021
Main
Amendment to ISO 15223-1:2021

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