注册

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

目录

基础信息

标准号
ISO 15223-1:2021/Amd 1:2025
版本
4
标准来源
ISO
标准发布组织
ISO
国际组织机构
ISO/TC 210    
标准语言
EN
发布日期
2025-03-03