Paragraph 9 F1
England, Wales and Scotland
In Annex 8—
in the title for “when designating inspection bodies to be notified” substitute “when designating approved bodies”;
in Section 1 for “authorized representative” substitute “UK responsible person”;
in Section 3 omit the words “and for which it has been notified”;
in Section 6 omit from “unless liability” to the end;
in Section 7 omit from “(except vis-à-vis” to the end.
Annotations
Textual amendments
- F1
Sch. 2A inserted (E.W.S.) (31.12.2020) by The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/791), regs. 1(1), 12 (as amended by S.I. 2020/1478, regs. 1(3), Sch. 2 paras. 2, 56, 57); 2020 c. 1, Sch. 5 para. 1(1)
- F2
Sch. 2A para. 9(aa) inserted (11.8.2021) by The Medical Devices (Amendment) (EU Exit) Regulations 2021 (S.I. 2021/873), reg. 1(1), Sch. 1 para. 21(e)