# The Medical Devices Regulations 2002, Paragraph 19


In Annex VIII—
(a) in Section 1, for “authorized representative” substitute “UK responsible person”;
(b) in Section 2.2 in the seventh indent for “Directive 2003/32/EC” substitute “Regulation 722/2012”;
(c) in Section 3, for “competent national authorities” substitute “Secretary of State”;
(d) in Sections 3.1 and 3.2, for “this Directive” each time it occurs substitute “the Regulations”;
(e) in Section 3.2—
(i) in the fourth indent, for “Article 5” in both places it occurs substitute “regulation 3A of the Regulations”;
(ii) in the sixth indent, for “Directive 2003/32/EC” substitute “Regulation 722/2012”;
(f) omit Section 5.

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Source: https://www.legislation.gov.uk/uksi/2002/618/schedule/2A/paragraph/19 (the official version)
Page: https://openlegislation.uk/medical-devices-regulations-2002/schedule-2A/paragraph-19
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.