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 CouncilText with EEA relevance.

32022R1107

Den Europæiske UnionForordning2022

European Union

Metadata

Type: Forordning
År: 2022
Ikrafttrædelsesdato: 1. januar 1970

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 CouncilText with EEA relevance. | TheLawyer.sh