# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 7.2

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

Other notified bodies may obtain a copy of the EC type-examination certificates and/or the supplements thereto. The Annexes to the certificates must be made available to other notified bodies on reasoned application, after the manufacturer has been informed.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/III/division/7/division/7.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-III/division-7/division-7.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

