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EVS-EN ISO 15223-1:2021/A1:2025

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 (ISO 15223 1:2021/Amd 1:2025)

General information

Valid from 01.12.2025
Estimated date of Estonian translation publication: 03.2026
Base Documents
ISO 15223-1:2021/Amd 1:2025; EN ISO 15223-1:2021/A1:2025
Directives or regulations
None

Standard history

Status
Date
Type
Name
01.12.2025
Amendment
01.12.2025
Main + amendment
01.10.2021
Main
Amendment to EN ISO 15223-1:2021

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