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Main page>UNE EN ISO 15223-1:2022/A1:2026 - 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)
Released: 2026-07-22
UNE EN ISO 15223-1:2022/A1:2026 - 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)

UNE EN ISO 15223-1:2022/A1:2026

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)

Productos sanitarios. Símbolos a utilizar con la información a suministrar por el fabricante. Parte 1: Requisitos generales. Modificación 1: Adición del término definido para representante autorizado y modificación del símbolo EC REP para que no sea específico de un país o región (ISO 15223 1:2021/Amd 1:2025)

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English PDF
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110.00 USD
English Hardcopy
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Spanish PDF
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Spanish Hardcopy
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Standard number:UNE EN ISO 15223-1:2022/A1:2026
Released:2026-07-22
Status:Amendment
Pages (English):39
Pages (Spanish):37
DESCRIPTION

UNE EN ISO 15223-1:2022/A1:2026

The draft European Standard does not contain this chapter.

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