Part 2A Making available on the market and putting into service under Regulation (EU) 2017/746F1
- 10ACertificates of free sale under Regulation (EU) 2017/746 – fee
- 10BRetention of documentation relating to conformity assessments
- 10CUK(NI) indication under Regulation (EU) 2017/746
Annotations
Textual amendments
- F1
Pt. 2A inserted (21.3.2024) by The Medical Devices (In Vitro Diagnostic Devices etc.) (Amendment) Regulations 2024 (S.I. 2024/221), regs. 1(2), 33