- Draft legislation
This is a draft item of legislation. This draft has since been made as a UK Statutory Instrument: The Medical Devices (Northern Ireland Protocol) Regulations 2021 No. 905
Draft Regulations laid before Parliament under paragraphs 8F(1) and 12(1) of Schedule 7 to the European Union (Withdrawal) Act 2018, for approval by resolution of each House of Parliament.
Draft Statutory Instruments
Medical Devices
Consumer Protection
Made
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Coming into force
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The Secretary of State, in exercise of the powers conferred by section 8C of, and paragraph 1(1)(ab) of Schedule 4, and paragraph 21 of Schedule 7 to, the European Union (Withdrawal) Act 2018(1), makes the following Regulations.
A draft of this instrument has been approved by a resolution of each House of Parliament, in accordance with paragraphs 8F(1)(2) and 12(1) of Schedule 7 to that Act.
The Treasury has consented to the making of these Regulations as required by paragraph 3(1) of Schedule 4 to that Act.
2018 c.16. The European Union (Withdrawal) Act 2018 was amended by the European Union (Withdrawal Agreement) Act 2020 (c. 1) (“the 2020 Act”). Section 8C was inserted by section 21 of the 2020 Act, and paragraph 1(1)(ab) of Schedule 4 by section 28 of that Act. Paragraph 21 of Schedule 7 was amended by paragraph 53(2) of Schedule 5 to the 2020 Act.
Paragraph 8F was inserted by paragraph 51 of Schedule 5 to the 2020 Act.
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