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EN ISO 15223-1:2021/prA1

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/DAM 1:2024)

General information

Draft
Base Documents
ISO 15223-1:2021/DAmd 1; EN ISO 15223-1:2021/prA1
Directives or regulations
None
You can view draft standards in the Commenting portal🡭.

Standard history

Status
Date
Type
Name
Amendment to EN ISO 15223-1:2021

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