ISO 15223-1:2021/Amd 1:2025
(Amendment)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
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
Dispositifs médicaux — Symboles à utiliser avec les informations à fournir par le fabricant — Partie 1: Exigences générales — Amendement 1: Ajout du terme défini représentant autorisé (mandataire) et modification du symbole EC REP pour ne pas être spécifique d’un pays ou d’une région
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ISO 15223-1
Fourth edition
Medical devices — Symbols to
2021-07
be used with information to be
supplied by the manufacturer —
AMENDMENT 1
2025-03
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
Dispositifs médicaux — Symboles à utiliser avec les informations
à fournir par le fabricant —
Partie 1: Exigences générales
AMENDEMENT 1: Ajout du terme défini représentant autorisé
(mandataire) et modification du symbole EC REP pour ne pas
être spécifique d’un pays ou d’une région
Reference number
ISO 15223-1:2021/Amd.1:2025(en) © ISO 2025
ISO 15223-1:2021/Amd.1:2025(en)
© ISO 2025
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ii
ISO 15223-1:2021/Amd.1:2025(en)
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