摘要
整理医疗器械产品技术要求的相关文件,并探讨其在医疗器械监督抽查检验工作中起的作用及发现的问题。
This article collects relevant documents of CFDA,and discusses the role of product technical requirements in sampling inspection of medical device and the detected problems.
作者
王博
王真
Wang Bo;Wang Zhen(Liaoning Medical Device Test Institute,Shenyang Liaoning 110179,China)
出处
《医疗装备》
2018年第15期47-48,共2页
Medical Equipment
关键词
产品技术要求
医疗器械
抽检
Product technical requirements
Sampling inspection of medical device
