Commission Implementing Regulation (EU) 2022/1107 of 4 July 2022 laying down common specifications for certain class D in vitro diagnostic medical devices in accordance with Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance)
Information
Type
Implementing regulation
Regulated products
IVDMD, Medical Devices
Published
July 4, 2022
Last updated
July 4, 2022
Description
Commission Implementing Regulation (EU) 2022/1107 sets common specifications for certain class D in vitro diagnostic medical devices in accordance with Regulation (EU) 2017/746.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0