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Division I CODES REFLECTING THE DESIGN AND INTENDED PURPOSE OF THE DEVICEF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 1Devices intended to be used for blood grouping
  2. 2Devices intended to be used for tissue typing
  3. 3Devices intended to be used for markers of cancer and non-malignant tumours
  4. 4Devices intended to be used for human genetic testing
  5. 5Devices intended to be used to determine markers of infections/immune status
  6. 6Devices intended to be used for non-infectious pathologies, physiological markers, disorders/impairments (except human genetic testing), and therapeutic measures
  7. 7Devices which are controls without a quantitative or qualitative assigned value
  8. 8Class A devices in sterile condition

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))