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Division 20 Label and instructions for useF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 20.1General requirements regarding the information supplied by the manufacturer
  2. 20.2Information on the label
  3. 20.3Information on the packaging which maintains the sterile condition of a device (‘sterile packaging’):
  4. 20.4Information in the instructions for use

Annotations

Textual amendments

F1

Regulation revoked (31.12.2020) by The Medical Devices Regulations 2002 (S.I. 2002/618), reg. 4P (as inserted by S.I. 2019/791, regs. 1(1), 3(7) (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 paras. 2, 9(m)); 2020 c. 1, Sch. 5 para. 1(1))