# 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 type-examination is the part of the procedure whereby a notified body ascertains and certifies that a representative sample of the production envisaged fulfils the relevant provisions of this Directive.

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