What you need to know about Regulation (EU) 2017/745? This factsheet is aimed at manufacturers of Class I medical devices. It covers devices that have already been placed on the market under Directive 93/42/EEC (MDD) and new devices intended to be placed on the market for the first time in accordance with Regulation (EU) 2017/745 of the European Parliament and the Council of 5 April 2017 (MDR).
April 29, 2021