Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for European Union reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)
Information
Type
Implementing regulation
Regulated products
IVDMD, Medical Devices
Published
June 17, 2022
Last updated
June 17, 2022
Description
Commission Implementing Regulation (EU) 2022/944 lays down rules for the application of Regulation (EU) 2017/746 on in vitro diagnostic medical devices.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0