# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 2.4

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

If the device is not intended to be used solely or principally in a specific part of the body, it must be considered and classified on the basis of the most critical specified use.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/IX/division/II/division/2/division/2.4 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-IX/division-II/division-2/division-2.4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.