# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 1.1d

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

Where demonstration of conformity with essential requirements based on clinical data is not deemed appropriate, adequate justification for any such exclusion has to be given based on risk management output and under consideration of the specifics of the device/body interaction, the clinical performances intended and the claims of the manufacturer. Adequacy of demonstration of conformity with the essential requirements by performance evaluation, bench testing and pre-clinical evaluation alone has to be duly substantiated.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/X/division/1/division/1.1d (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-X/division-1/division-1.1d
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.