# The Medical Devices Regulations 2002, Paragraph 26


In Annex III—
(a) in the title and in Section 1, omit “EC”;
(b) in Section 1—
(i) for “authorised representative” substitute “UK responsible person”;
(ii) for “this Directive” substitute “the Regulations”;
(iii) for “CE marking in accordance with Article 16” substitute “UK marking in accordance with regulation 36 of the Regulations”;
(c) in Section 3, for “the Directive” in both places substitute “the Regulations”;
(d) in Section 3, in the sixth indent, for “Article 5” in both places substitute “regulation 3A of the Regulations”;
(e) omit Section 5;
(f) in Section 6, for “a notified body” substitute “an approved body”;
(g) in Section 6.2—
(i) for “notified body”, both times those words occur, substitute “approved body”;
(ii) in the first sentence, for “this Directive” substitute “the Regulations”;
(iii) in the second sentence omit “of the Directive”;
(iv) for “an EC” substitute “a” ;
(h) in Section 6.3—
(i) for “notified body” in both places substitute “approved body”;
(ii) omit each reference to “EC”;
(iii) for “the Directive” substitute “the Regulations”.

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Source: https://www.legislation.gov.uk/uksi/2002/618/schedule/2A/paragraph/26 (the official version)
Page: https://openlegislation.uk/medical-devices-regulations-2002/schedule-2A/paragraph-26
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.