# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 1

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

The manufacturer must ensure application of the quality system approved for the manufacture of the products concerned and carry out the final inspection, as specified in Section 3, and is subject to the Community surveillance referred to in Section 4.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/V/division/1 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-V/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.