# Commission Decision of 7 May 2002 on common technical specifications for in vitro-diagnostic medical devices (notified under document number C(2002) 1344) (Text with EEA relevance) (2002/364/EC), Division: Rapid test

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

‘Rapid test’ means qualitative or semi-quantitative in vitro diagnostic medical devices, used singly or in a small series, which involve non-automated procedures and have been designed to give a fast result.

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Source: https://www.legislation.gov.uk/eudn/2002/364/annex/division/2/division/10 (the official version)
Page: https://openlegislation.uk/eu-decision-2002-364/annex/division-2/division-10
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.