# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 1

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

EC verification is the procedure whereby the manufacturer or his authorized representative established in the Community 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/1993/42/annex/IV/division/1 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-IV/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.