DS/EN ISO 15223-1:2021/A1:2025
Current
Current
The latest, up-to-date edition.
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)
Amendment of
Published date
20-11-2025
Publisher
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This document identifies requirements for symbols used in medical device labelling that convey information on the safe and effective use of medical devices. It also lists symbols that satisfy the requirements of this document.
| Committee |
DS/S-257
|
| DocumentType |
Amendment
|
| PublisherName |
Danish Standards
|
| Status |
Current
|
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