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 relev
2017年11月23日关于代码和相应类型设备清单的委员会实施条例(EU)2017/2185 目的是根据欧洲议会和理事会条例(EU)2017/745规定指定为医疗设备领域的公告机构 并根据欧洲委员会条例(EU)2017/746规定指定为体外诊断医疗设备议会和理事会(EEA版本的文本)
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. )