# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 3

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

The devices must achieve the performances intended by the manufacturer and be designed, manufactured and packaged in such a way that they are suitable for one or more of the functions referred to in Article 1 (2) (a), as specified by the manufacturer.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/I/division/I/division/3 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-I/division-I/division-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.