# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 3.1

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

If the device is intended for use in combination with other devices or equipment, the whole combination, including the connection system, must be safe and must not impair the specified performances of the devices. Any restrictions on use must be indicated on the label and/or in the instructions for use.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/I/division/B/division/3/division/3.1 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-I/division-B/division-3/division-3.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.