The following documents shall be added. In case of extension or renewal, only new or modified documents shall be submitted.
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)
The following documents shall be added. In case of extension or renewal, only new or modified documents shall be submitted.