Eurlex法规编号：	(EU) 2017/2185
OJ编号：	OJ L 309, 24.11.2017, p. 7–17
中文标题：	2017年11月23日委员会实施条例(EU) 2017/2185：关于明确在欧盟议会和欧盟理事会(EU) 2017/745号条例中所指定医疗器械领域的认证机构、欧洲议会和理事会(EU) 2017/746号条例中载明的体外诊断医疗器械的代码列表和相应类型的设备
原文标题：	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)
发布日期	2017-11-16
原文链接	查看欧盟官网文件