# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 8.2

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

in derogation from Sections 1, 2, 5 and 6, the verifications conducted by the notified body are intended to confirm the conformity of the products in Class IIa with the technical documentation referred to in Section 3 of Annex VII.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/IV/division/8/division/8.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-IV/division-8/division-8.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.