# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 5.1

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

Every product is examined individually and the appropriate tests defined in the relevant standard(s) referred to in Article 5 or equivalent tests must be carried out in order to verify, where appropriate, the conformity of the products with the EC type described in the type-examination certificate and with the requirements of the Directive which apply to them.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/IV/division/5/division/5.1 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-IV/division-5/division-5.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.