Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin Text with EEA relevance
Information
Type
Regulation
Regulated products
Medical Devices
Published
August 8, 2012
Last updated
August 8, 2012
Description
Commission Regulation (EU) No. 722/2012 sets specific requirements for active implantable medical devices and medical devices made from animal tissues.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0