On the new regulation of medical devices in Europe

被引：25
|
作者：
Migliore, Antonio [1 ]
机构：
[1] Agenas, Agenzia Nazl & Serv Sanitari Reg, Innovat & Dev Dept, Rome, Italy
来源：
EXPERT REVIEW OF MEDICAL DEVICES | 2017年 / 14卷 / 12期
关键词：
Medical devices; regulation; CE mark; high-risk; class III; Europe;
D O I：
10.1080/17434440.2017.1407648
中图分类号：
R318 [生物医学工程];
学科分类号：
0831 ;
摘要：
引用
收藏
页码：921 / 923
页数：3
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