# Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, Division 13.5

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

Wherever reasonable and practicable, the devices and detachable components must be identified, where appropriate in terms of batches, to allow all appropriate action to detect any potential risk posed by the devices and detachable components.

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Source: https://www.legislation.gov.uk/eudr/1993/42/annex/I/division/II/division/13/division/13.5 (the official version)
Page: https://openlegislation.uk/eu-directive-1993-42/annex-I/division-II/division-13/division-13.5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.