# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 5

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

The devices must be designed, manufactured and packed in such a way that their characteristics and performances during their intended use will not be adversely affected during transport and storage taking account of the instructions and information provided by the manufacturer.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/I/division/I/division/5 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-I/division-I/division-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.