# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 8.7

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

The packaging and/or label of the device must distinguish between identical or similar products sold in both sterile and non-sterile condition.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/I/division/II/division/8/division/8.7 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-I/division-II/division-8/division-8.7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.