# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 6.2

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

For devices in Class IIa the notified body shall assess, as part of the assessment in Section 3.3, the technical documentation as described in Section 3 of Annex VII for at least one representative sample for each device subcategory for compliance with the provisions of this Directive.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/V/division/6/division/6.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-V/division-6/division-6.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.