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Consumer Rights Act 2015

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Changes over time for: Cross Heading: Power to decommission or switch off fixed installations

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Changes to legislation:

Consumer Rights Act 2015, Cross Heading: Power to decommission or switch off fixed installations is up to date with all changes known to be in force on or before 09 June 2025. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations. Help about Changes to Legislation

Power to decommission or switch off fixed installationsU.K.

30(1)The power in sub-paragraph (2) is available to an officer of a domestic enforcer acting pursuant to the duty in [F1regulation 52(1)(a)(ii) or (b)(ii) of the Electromagnetic Compatibility Regulations (S.I. 2016/1091)].U.K.

(2)The officer may decommission or switch off any fixed installation (as defined in those Regulations) or part of such an installation.

Textual Amendments

F1Words in Sch. 5 para. 30(1) substituted (8.12.2016) by The Electromagnetic Compatibility Regulations 2016 (S.I. 2016/1091), regs. 1, 76(4)(d) (with reg. 75(3))

Commencement Information

I1Sch. 5 para. 30 in force at 27.5.2015 for specified purposes for E. by S.I. 2015/965, art. 2(b)

I2Sch. 5 para. 30 in force at 27.5.2015 for specified purposes by S.I. 2015/1333, art. 2(a)

I3Sch. 5 para. 30 in force at 1.10.2015 in so far as not already in force by S.I. 2015/1630, art. 3(h) (with art. 8)

[F230A(1)The power in sub-paragraph (2) is available to an officer of a domestic enforcer acting [F3pursuant to— U.K.

(a)the duty in regulation 61(1A) or (1B) of the Medical Devices Regulations 2002 (S.I. 2002/618),

(b)a duty in regulations made under section 15(1) of the Medicines and Medical Devices Act 2021, or

(c)the duty in regulation 26 of the Medical Devices (Northern Ireland Protocol) Regulations 2021.]

(2)The officer may decommission or switch off any [F4relevant medical device] which is installed at a given location.

[F5(3)In sub-paragraph (2), “relevant medical device” means—

(a)where a domestic enforcer is acting pursuant to a duty mentioned in sub-paragraph (1)(a) or (b), any medical device to which the Medical Devices Regulations 2002 apply;

(b)where a domestic enforcer is acting pursuant to the duty mentioned in sub-paragraph (1)(c), any medical device to which Regulation (EU) 2017/745 on medical devices [F6or Regulation (EU) 2017/746 on in vitro diagnostic medical devices] applies.]]

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