SIST EN ISO 15223-1:2021/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)
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)
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 38
- Дата публикации:
- 24 ноября 2025 г.
- Издание:
- ISO 15223 1:2021/Amd 1:2025
- ICS:
- 01.080.20
Abstract
Overview
EN ISO 15223-1:2021/A1:2025 is a CEN-adopted amendment to the international standard on used in manufacturer-supplied information. This Amendment 1 (/Amd 1:2025) adds a defined term for and updates the so it is not specific to any single country or region. The document was approved by CEN and is intended to be implemented into national standards by May 2026.
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