Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance)

欧盟 · 最近核对：2026-09-08

编号

32017R2185

类型

法规/条例

颁布机关

European Commission

状态

in_force

主管机构

欧盟委员会 / MDCG

这份文件管什么

规定公告机构指定范围所用的器械代码表（MD/IVD/MDS/MDT 等代码）；判断某公告机构能否受理你的产品，查的就是这张代码表。

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