MEDICAL DEVICES

IN VITRO DIAGNOSTIC MEDICAL DEVICES

The Medical Device Regulation (MDR)

Regulation (EU) 2017/745 of the European Parliament and of the Council

of 5 April 2017

on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC