- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (a wnaed Fel)
Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol).
18. An importer shall not place a product on the market unless it is in conformity with the essential health and safety requirements.
19.—(1) Before placing a product on the market, an importer shall ensure that—
(a)a relevant conformity assessment procedure has been carried out by the manufacturer;
(b)the manufacturer has drawn up the technical documentation;
(c)the product—
(i)bears the CE marking where applicable;
(ii)is accompanied by the EU declaration of conformity or the attestation of conformity as appropriate; and
(iii)is accompanied by the required documents; and
(d)the manufacturer has complied with the requirements set out in regulation 11 (Labelling and packaging of products), regulation 12 (Labelling and packaging of products, other than components) and regulation 13 (Information identifying manufacturer).
(2) In paragraph (1)(c)(iii), “required documents” means any documents that are required to be provided with a product pursuant to—
(a)regulation 11(2) (Labelling and packaging of products);
(b)regulation 13(2)(b) (Information identifying manufacturer);
(c)regulation 14(1) (Instructions and safety information).
20.—(1) Where an importer considers, or has reason to believe, that a product is not in conformity with the essential health and safety requirements, the importer shall not place the product on the market.
(2) Where the product presents a risk, the importer shall inform the manufacturer and the market surveillance authority of that risk.
21.—(1) Before placing a product on the market, an importer shall indicate on the product—
(a)the name, registered trade name or registered trade mark of the importer; and
(b)a postal address at which the importer can be contacted.
(2) The information specified in paragraph (1) shall be in a language which can be easily understood by end-users and by the competent national authority in the Member State in which it is to be made available to end-users.
(3) Where it is not possible to indicate the information specified in paragraph (1) on the product, the importer shall indicate that information—
(a)on the packaging; or
(b)in a document accompanying the product.
22.—(1) When placing a product on the market, an importer shall ensure that it is accompanied by instructions and safety information in a language which can be easily understood by end-users in the Member State in which the product is to be made available.
(2) Where the Member State referred to in paragraph (1) is the United Kingdom, the language referred to in that paragraph shall be English.
23. Each importer shall ensure that, whilst a product is under that importer’s responsibility, its storage or transport conditions do not jeopardise its conformity with the essential health and safety requirements.
24.—(1) When deemed appropriate, with regard to the risks to the health and safety of end-users presented by a product, an importer shall—
(a)carry out sample testing of a product made available by the importer on the market;
(b)investigate complaints that a product placed on the market by the importer is not in conformity with Part 2; and
(c)keep distributors informed of actions carried out under sub-paragraphs (a) and (b).
(2) An importer shall keep a register of—
(a)complaints that a product is not in conformity with Part 2;
(b)products which are found not to be in conformity with Part 2; and
(c)product recalls.
(3) An importer shall keep an entry made in the register for a period of at least 10 years beginning on the day on which the obligation to make the entry arose.
25.—(1) An importer who considers, or has reason to believe, that a product which the importer has placed on the market is not in conformity with Part 2 shall immediately take the corrective measures necessary to—
(a)bring the product into conformity;
(b)withdraw the product; or
(c)recall the product.
(2) Where the product presents a risk, the importer shall immediately inform the market surveillance authority, and the competent national authorities of any other Member State in which the importer made the product available on the market, of the risk, giving details of—
(a)the respect in which the product is considered not to be in conformity with Part 2; and
(b)any corrective measures taken.
26.—(1) An importer shall, further to a reasoned request from the market surveillance authority and within such period as the market surveillance authority may specify, provide the authority with the information and documentation necessary to demonstrate that the product is in conformity with Part 2—
(a)in paper or electronic form; and
(b)in a language which can be easily understood by the market surveillance authority.
(2) An importer shall, at the request of the market surveillance authority, cooperate with the authority on any action taken to—
(a)evaluate a product in accordance with regulation 55 (Evaluation of a product presenting a risk);
(b)eliminate the risks posed by the product which the importer has placed on the market.
27. An importer shall, for a period of ten years beginning on the day on which the product was placed on the market, keep and, upon request, make available to the market surveillance authority—
(a)a copy of the EU declaration of conformity or, where applicable, the attestation of conformity; and
(b)the technical documentation.
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.
Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Rule and provides information about its policy objective and policy implications. They aim to make the Statutory Rule accessible to readers who are not legally qualified and accompany any Northern Ireland Statutory Rule or Draft Northern Ireland Statutory Rule laid before the UK Parliament during the suspension of the Northern Ireland Assembly.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys