# Commission Implementing Regulation (EU) No 920/2013 of 24 September 2013 on the designation and the supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42/EEC on medical devices (Text with EEA relevance), Article 2: Interpretation of designation criteria

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

The criteria set out in Annex 8 to Directive 90/385/EEC or in Annex XI to Directive 93/42/EEC shall be applied as laid down in Annex I.

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Source: https://www.legislation.gov.uk/eur/2013/920/article/2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-920/article-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.