Commission Implementing Regulation (EU) No 920/2013 of 24 September 2013 on the designation and the supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42/EEC on medical devices Text with EEA relevance
Information
Type
Implementing regulation
Regulated products
Medical Devices
Published
September 24, 2013
Last updated
September 24, 2013
Description
Commission Implementing Regulation (EU) No. 920/2013 on the designation and supervision of notified bodies for medical devices.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0