# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 5.2

Extent: E+W+S+N.I.

The notified body must affix, or have affixed its identification number to each approved product and must draw up a written certificate of conformity relating to the tests carried out.

---
Source: https://www.legislation.gov.uk/eudr/1993/42/annex/IV/division/5/division/5.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-IV/division-5/division-5.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.