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Annex II The list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of in vitro diagnostic medical devices under Regulation (EU) 2017/746F1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. ICODES REFLECTING THE DESIGN AND INTENDED PURPOSE OF THE DEVICE
  2. IIHORIZONTAL CODES

Annotations

Textual amendments

F1

Regulation revoked (with saving) (31.12.2020) by S.I. 2002/618, reg. 4M (as inserted by The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/791), regs. 1(1), 3(7) (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 para. 2); 2020 c. 1, Sch. 5 para. 1(1))