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DIN EN ISO 15223-1:2026

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021 + Amd. 1:2025); German version EN ISO 15223-1:2021 + A1:2025

This document identifies requirements for symbols used in medical device labelling that may convey information on the safe and effective use of medical devices. The Amendment includes the addition of defined term for authorized representative (clause 3.20), modified EC REP symbol to not be country or region specific (Item 5.1.2 in Table 1 and A.4 in Annex A)

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Deutsches Institut für Normung [din]

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