# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 7: Administrative provisions

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 available to the other notified bodies on reasoned application, after the manufacturer has been informed.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/V/division/7 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-V/division-7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.