# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 7.3

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

The manufacturer or his authorised representative must keep with the technical documentation copies of EC type-examination certificates and their additions for a period ending at least five years after the last device has been manufactured. In the case of implantable devices, the period shall be at least 15 years after the last product has been manufactured.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/III/division/7/division/7.3 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-III/division-7/division-7.3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.