# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 6.2

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

The manufacturer may place the devices on the market, unless the notified body communicates to the manufacturer within the agreed time-frame, but not later than 30 days after reception of the samples, any other decision, including in particular any condition of validity of delivered certificates.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/IV/division/6/division/6.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-IV/division-6/division-6.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.