- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (31/12/2022)
- Gwreiddiol (a wnaed Fel)
Point in time view as at 31/12/2022.
There are currently no known outstanding effects for the The Electromagnetic Compatibility Regulations 2016, PART 3.
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39.—(1) Equipment which is in conformity with a [F1designated] standard (or part of such a standard) F2... is to be presumed to be in conformity with the essential requirements covered by that standard (or that part of that standard).
(2) The presumption in paragraph (1) is rebuttable.
Extent Information
E1This version of this provision extends to England, Wales and Scotland only; a separate version has been created for Northern Ireland only
Textual Amendments
F1Word in reg. 39(1) substituted (E.W.S.) (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 20 para. 25(a) (with Sch. 20 para. 33) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)
F2Words in reg. 39(1) omitted (E.W.S.) (31.12.2020) by virtue of The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 20 para. 25(b) (with Sch. 20 para. 33) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)
39.—(1) Equipment which is in conformity with a harmonised standard (or part of such a standard) the reference to which has been published in the Official Journal is to be presumed to be in conformity with the essential requirements covered by that standard (or that part of that standard).
(2) The presumption in paragraph (1) is rebuttable.
40.—(1) Subject to paragraph (2), the manufacturer must demonstrate the conformity of the apparatus with the essential requirements by means of either—
(a)the procedure set out in Schedule 2 (Module A: internal production control); or
(b)the procedures set out in Schedule 3 (Module B: EU type examination followed by Module C: conformity to type based on internal production control).
(2) The manufacturer may choose to demonstrate the conformity of apparatus with some of the essential requirements by following the procedure referred to in paragraph (1)(b) provided that the procedure referred to in paragraph (1)(a) is followed for the remaining essential requirements.
41. The F4... declaration of conformity for apparatus must—
(a)state that the fulfilment of the essential requirements has been demonstrated in respect of the apparatus;
(b)contain the elements of the relevant conformity assessment procedure or procedures followed in respect of the apparatus; and
(c)have the model structure set out in Schedule 4.
Extent Information
E2This version of this provision extends to England, Wales and Scotland only; a separate version has been created for Northern Ireland only
Textual Amendments
F3Word in reg. 41 heading substituted (E.W.S.) (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 20 para. 26(a) (with Sch. 20 para. 33) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)
F4Word in reg. 41 omitted (E.W.S.) (31.12.2020) by virtue of The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 20 para. 26(b) (with Sch. 20 para. 33) (as amended by S.I. 2020/676, regs. 1(1), 2); 2020 c. 1, Sch. 5 para. 1(1)
41. The EU declaration of conformity for apparatus must—
(a)state that the fulfilment of the essential requirements has been demonstrated in respect of the apparatus;
(b)contain the elements of the relevant conformity assessment procedure or procedures followed in respect of the apparatus; and
(c)have the model structure set out in Schedule 4.
42.—[F6(1) The UK marking must be affixed visibly, legibly and indelibly—
(a)to the apparatus;
(b)to its data plate; or
(c)where paragraph (1A) applies, to—
(i)a label affixed to the apparatus or its data plate; or
(ii)to a document accompanying the apparatus.]
[F7(1A) For a period of [F8seven years] beginning with IP completion day, the UK marking may be affixed to—
(a)a label affixed to the apparatus or its data plate; or
(b)a document accompanying the apparatus.]
(2) Where [F9paragraph (1A) does not apply and] it is not possible or warranted, on account of the nature of the apparatus, to affix the [F10UK] marking in accordance with paragraph (1), the CE marking must be affixed to—
(a)the packaging; and
(b)the accompanying documents.
Extent Information
E3This version of this provision extends to England, Wales and Scotland only; a separate version has been created for Northern Ireland only
Textual Amendments
F5Word in reg. 42 heading substituted (E.W.S.) (31.12.2020) by S.I. 2019/696, Sch. 20 para. 27(a) (as substituted by The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020 (S.I. 2020/1460), reg. 1(4), Sch. 3 para. 12(4))
F6Reg. 42(1) substituted (E.W.S.) (31.12.2020) by S.I. 2019/696, Sch. 20 para. 27(b) (as substituted by The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020 (S.I. 2020/1460), reg. 1(4), Sch. 3 para. 12(4))
F7Reg. 42(1A) inserted (E.W.S.) (31.12.2020) by S.I. 2019/696, Sch. 20 para. 27(c) (as substituted) by The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020 (S.I. 2020/1460), reg. 1(4), Sch. 3 para. 12(4))
F8Words in reg. 42(1A) substituted (E.W.S.) (31.12.2022) by The Product Safety and Metrology (Amendment and Transitional Provisions) Regulations 2022 (S.I. 2022/1393), regs. 1(1), 3, Sch. 2 para. (i)
F9Words in reg. 42(2) inserted (E.W.S.) (31.12.2020) by S.I. 2019/696, Sch. 20 para. 27(d) (as substituted by The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020 (S.I. 2020/1460), reg. 1(4), Sch. 3 para. 12(4))
F10Word in reg. 42(2) substituted (E.W.S.) (31.12.2020) by S.I. 2019/696, Sch. 20 para. 27(a) (as substituted by The Product Safety and Metrology etc. (Amendment etc.) (UK(NI) Indication) (EU Exit) Regulations 2020 (S.I. 2020/1460), reg. 1(4), Sch. 3 para. 12(4))
42.—(1) The CE marking must be affixed visibly, legibly and indelibly to the apparatus or to its data plate.
(2) Where it is not possible or warranted, on account of the nature of the apparatus, to affix the CE marking in accordance with paragraph (1), the CE marking must be affixed to—
(a)the packaging; and
(b)the accompanying documents.
Extent Information
E4This version of this provision extends to Northern Ireland only; a separate version has been created for England, Wales and Scotland only
42A.—(1) Where the CE marking is affixed on the basis of an assessment or a certificate issued by a notified body established in the United Kingdom, a UK(NI) indication must be affixed in relation to the apparatus, in accordance with this regulation.
(2) The UK(NI) indication must be affixed—
(a)visibly, legibly and indelibly; and
(b)before apparatus is placed on the market in Northern Ireland.
(3) The UK(NI) indication must accompany the CE marking, wherever that is affixed in accordance with regulation 42.
(4) The UK(NI) indication must be affixed by—
(a)the manufacturer; or
(b)the manufacturer's authorised representative.
(5) When placing apparatus on the market in Northern Ireland, an importer must ensure that the manufacturer has complied with their obligations under this regulation.
Textual Amendments
42B.—(1) The Secretary of State must ensure that—
(a)each notified body established in the United Kingdom is assigned an identification number; and
(b)there is a register of—
(i)notified bodies established in the United Kingdom;
(ii)their notified body identification number;
(iii)the activities for which they have been notified;
(iv)any restrictions on those activities.
(2) The Secretary of State must ensure that the register referred to in paragraph (1) is maintained and made publicly available.
(3) The Secretary of State may authorise the United Kingdom Accreditation Service to compile and maintain the register in accordance with paragraph (1)(b).]
Textual Amendments
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