The technical specifications set out in the Annex to this Decision are adopted as common technical specifications for in vitro diagnostic medical devices in list A of Annex II to Directive 98/79/EC [F1as that Annex applied before IP completion day and as modified by Schedule 2A to the Medical Devices Regulations 2002].
Textual Amendments
F1Words in Art. 1 inserted (E.W.S.) (11.8.2021) by The Medical Devices (Amendment) (EU Exit) Regulations 2021 (S.I. 2021/873), reg. 1(1), Sch. 2 para. 1