# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 5.1

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

Devices shall be designed, manufactured and packaged in such a way that exposure of users and other persons to the emitted radiation is minimised.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/I/division/B/division/5/division/5.1 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-I/division-B/division-5/division-5.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.