# Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin (Text with EEA relevance), Division 18: Conclusion of this assessment:

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

Based on the evaluation of data and the assessment process it is our preliminary decision that the application meets the requirements of conformity with
 Part 3 of the Medical Devices Regulations 2002  Part 2 of the Medical Devices Regulations 2002
and Regulation (EU) No 722/2012.

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Source: https://www.legislation.gov.uk/eur/2012/722/annex/II/division/3/division/1/division/18 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-722/annex-II/division-3/division-1/division-18
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.