# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 7.2

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 3.2(c) 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/II/division/7/division/7.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-II/division-7/division-7.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.