# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic 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.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/VI/division/5/division/5.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-VI/division-5/division-5.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.