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

页码：921 / 923

页数：3

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