# Council Directive of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (90/385/EEC), Division 7.3

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

The manufacturer or his authorized representative shall keep with the technical documentation a copy of the EC type-examination certificates and the supplements to them for a period of at least 15 years from the manufacture of the last product .

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Source: https://www.legislation.gov.uk/eudr/1990/385/annex/3/division/7/division/7.3 (the official version)
Page: https://openlegislation.uk/eu-directive-1990-385/annex-3/division-7/division-7.3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.