Commission Implementing Regulation (EU) 2022/2347 of 1 December 2022 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards reclassification of groups of certain active products without an intended medical purpose (Text with EEA relevance)
Information
Type
Implementing regulation
Regulated products
Medical Devices
Published
December 1, 2022
Last updated
December 1, 2022
Description
Commission Implementing Regulation (EU) 2022/2347 establishes rules for reclassifying certain active products without a medical purpose.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0