1. | The responsible person must, for each type, draw up the technical file referred to in Annex VII (Part 7 of this Schedule), part A. |
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2. | For each type, the application for [an EC type-] [a Type-] examination shall be submitted by the responsible person to [a notified] [an approved ] body chosen by the responsible person. |
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| The application shall include: |
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| the name and address of the manufacturer and, where appropriate, the manufacturer's authorised representative, |
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| a written declaration that the application has not been submitted to another notified body, |
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| the technical file. |
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| Moreover, the applicant shall place at the disposal of the [notified] [approved] body a sample of the type. The [notified] [approved] body may ask for further samples if the test programme so requires. |
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3. | The [notified] [approved] body shall: |
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3.1. | examine the technical file, check that the type was manufactured in accordance with it and establish which elements have been designed in accordance with the relevant provisions of published harmonised standards, and those elements whose design is not based on the relevant provisions of those standards; |
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3.2. | carry out or have carried out appropriate inspections, measurements and tests to ascertain whether the solutions adopted satisfy the essential health and safety requirements, where [published harmonised] [designated] standards were not applied; |
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3.3. | where [published harmonised] [designated] standards were used, carry out or have carried out appropriate inspections, measurements and tests to verify that those standards were actually applied; |
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3.4. | agree with the applicant as to the place where the check that the type was manufactured in accordance with the examined technical file and the necessary inspections, measurements and tests will be carried out. |
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4. | If the type satisfies the provisions of [the Directive] [these Regulations], the [notified] [approved] body shall issue the applicant with [an EC type-] [a Type-] examination certificate. The certificate shall include the name and address of the manufacturer and the manufacturer's authorised representative, the data necessary for identifying the approved type, the conclusions of the examination and the conditions to which its issue may be subject. |
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| The manufacturer and the [notified] [approved] body shall retain a copy of this certificate, the technical file and all relevant documents for a period of 15 years from the date of issue of the certificate. |
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5. | [If the type does not satisfy the provisions of the Directive, the notified body shall refuse to issue the applicant with an EC type-examination certificate, giving detailed reasons for its refusal. It shall inform the applicant, the other notified bodies and the Member State which notified it. An appeal procedure must be available.] [If the type does not satisfy the provisions of these Regulations, the approved body shall refuse to issue the applicant with a Type-examination certificate, giving detailed reasons for its refusal. It shall inform the applicant, the other approved bodies and the Secretary of State. An appeal procedure must be available.] |
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6. | The applicant shall inform the [notified] [approved] body which retains the technical file relating to the [EC type-] [Type-] examination certificate of all modifications to the approved type. The [notified] [approved] body shall examine these modifications and shall then either confirm the validity of the existing [EC type-] [Type-] examination certificate or issue a new one if the modifications are liable to compromise conformity with the essential health and safety requirements or the intended working conditions of the type. |
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7. | The [Commission, the Member States] [Secretary of State] and the other [notified] [approved] bodies may, on request, obtain a copy of the [EC type-] [Type-] examination certificates. On reasoned request, the [Commission and the Member States] [Secretary of State] may obtain a copy of the technical file and the results of the examinations carried out by the [notified] [approved] body. |
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8. | [Files and correspondence referring to the EC type-examination procedures shall be written in the official language(s) of the [relevant] state where the notified body is established or in any other official Community language acceptable to the notified body.] [Files and correspondence referring to the Type-examination procedures shall be written in English or any other language acceptable to the approved body.] |
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9. | Validity of the [EC type-] [Type-] examination certificate |
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9.1. | The [notified] [approved] body has the ongoing responsibility of ensuring that the [EC type-] [Type-] examination certificate remains valid. It shall inform the manufacturer of any major changes which would have an implication on the validity of the certificate. The [notified] [approved] body shall withdraw certificates which are no longer valid. |
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9.2. | The manufacturer of the machinery concerned has the ongoing responsibility of ensuring that the said machinery meets the corresponding state of the art. |
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9.3. | The manufacturer shall request from the [notified] [approved] body the review of the validity of the [EC type-] [Type-] examination certificate every five years. |
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| If the notified body finds that the certificate remains valid, taking into account the state of the art, it shall renew the certificate for a further five years. |
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| The manufacturer and the notified body shall retain a copy of this certificate, of the technical file and of all the relevant documents for a period of 15 years from the date of issue of the certificate. |
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9.4. | In the event that the validity of the [EC-type] [Type-] examination certificate is not renewed, the manufacturer shall cease the placing on the market of the machinery concerned. |