# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 1

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

EC verification is the procedure whereby the manufacturer or his authorised representative ensures and declares that the products which have been subject to the procedure set out in section 4 conform to the type described in the EC type-examination certificate and meet the requirements of this Directive which apply to them.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/VI/division/1 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-VI/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.