# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 7.6

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

Devices must be designed and manufactured in such a way as to reduce, as much as possible, risks posed by the unintentional ingress of substances into the device taking into account the device and the nature of the environment in which it is intended to be used.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/I/division/II/division/7/division/7.6 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-I/division-II/division-7/division-7.6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.