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ANNEX IIIU.K.CONFORMITY ASSESSMENT PROCEDURES FOR SUBSYSTEMS AND SAFETY COMPONENTS: MODULE B: [F1TYPE] EXAMINATION — PRODUCTION TYPE

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1.[F2Type] examination is the part of a conformity assessment procedure in which [F3an approved body] examines the technical design of a subsystem or a safety component and verifies and attests that the technical design meets the requirements of this Regulation that apply to it.U.K.

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2.[F4Type] examination shall be carried out by assessment of the adequacy of the technical design of the subsystem or the safety component through examination of the technical documentation referred to in point 3, plus examination of a specimen, representative of the production envisaged, of the complete subsystem or safety component (production type).U.K.

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3.The manufacturer shall lodge an application for [F5type] examination with a [F6single approved body] of his choice.U.K.

The application shall include:

(a)

the name and address of the manufacturer and, if the application is lodged by the authorised representative, his name and address as well;

(b)

a written declaration that the same application has not been lodged with any [F7other approved body];

(c)

the technical documentation for the subsystem or the safety component according to Annex VIII;

(d)

a representative specimen of the subsystem or the safety component envisaged or details of the premises where it can be examined. [F8The approved body] may request further specimens if needed for carrying out the test programme.

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4.[F9The approved body] shall:U.K.

4.1.

examine the technical documentation to assess the adequacy of the technical design of the subsystem or the safety component;

4.2.

verify that the specimen(s) have been manufactured in conformity with the technical documentation, and identify the elements that have been designed in accordance with the applicable provisions of the [F10relevant designated standards], as well as the elements which have been designed in accordance with other relevant technical specifications;

4.3.

carry out appropriate examinations and tests, or have them carried out, to check whether, where the manufacturer has chosen to apply the solutions in the [F11relevant designated standards], these have been applied correctly;

4.4.

carry out appropriate examinations and tests, or have them carried out, to check whether, where the solutions in the [F12relevant designated standards] have not been applied, the solutions adopted by the manufacturer applying other relevant technical specifications meet the corresponding essential requirements of this Regulation;

4.5.

agree with the manufacturer on a location where the examinations and tests will be carried out.

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5.[F13The approved body] shall draw up an evaluation report that records the activities undertaken in accordance with point 4 and their outcomes. Without prejudice to its obligations vis-à-vis [F14the Secretary of State], [F15the approved body] shall release the content of that report, in full or in part, only with the agreement of the manufacturer.U.K.

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6.Where the type meets the requirements of this Regulation, [F16the approved body] shall issue [F17a type examination] certificate to the manufacturer. The certificate shall contain the name and address of the manufacturer, the conclusions of the examination, any conditions for its validity, the necessary data for identification of the approved type (subsystem or safety component) and if relevant, descriptions of its functioning. The certificate may have one or more annexes attached.U.K.

[F18The type examination] certificate and its annexes shall contain all relevant information to allow the conformity of manufactured subsystems and safety components with the examined type to be evaluated and to allow for in-service control. It shall also indicate any conditions to which its issue may be subject and be accompanied by the descriptions and drawings necessary for identification of the approved type.

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The certificate shall have a maximum validity period of 30 years from the date of its issue.

Where the type does not satisfy the applicable requirements of this Regulation, [F19the approved body] shall refuse to issue [F20a type examination] certificate and shall inform the applicant accordingly, giving detailed reasons for its refusal.

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7.[F21The approved body] shall keep itself apprised of any changes in the generally acknowledged state of the art which indicate that the approved type may no longer comply with the applicable requirements of this Regulation and shall determine whether such changes require further investigation. If so, [F22the approved body] shall inform the manufacturer accordingly.U.K.

The manufacturer shall inform [F23the approved body] that holds the technical documentation relating to [F24the type] examination certificate of any modifications to the approved type that may affect the conformity of the subsystem or the safety component with the essential requirements of this Regulation or the conditions for validity of the certificate.

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[F25The approved body] shall examine the modification and inform the manufacturer whether [F26the type examination] certificate remains valid or whether further examinations, verifications or tests are needed. As appropriate, [F27the approved body] shall issue an addition to [F28the original type] examination certificate or ask for a new application for [F29a type] examination to be submitted.

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8.[F30Each approved body] shall inform [F31the Secretary of State] concerning [F32the type] examination certificates and/or any additions thereto which it has issued or withdrawn, and shall, periodically or upon request, make available to [F31the Secretary of State] the list of such certificates and/or any additions thereto refused, suspended or otherwise restricted.U.K.

[F33Each approved body] shall inform [F34the other approved bodies] concerning [F35the type examination] certificates and/or any additions thereto which it has refused, withdrawn, suspended or otherwise restricted, and, upon request, concerning such certificates and/or additions thereto which it has issued.

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The F36... [F37other approved bodies] may, on request, obtain a copy of [F38the type examination] certificates and/or additions thereto. F39.... [F40The approved body] shall keep a copy of [F38the type examination] certificate, its annexes and additions, as well as the technical file including the documentation submitted by the manufacturer, until the expiry of the validity of that certificate.

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9.The manufacturer shall keep a copy of [F41the type] examination certificate, its annexes and additions together with the technical documentation at the disposal of [F42the Secretary of State] for 30 years after the subsystem or the safety component has been placed on the market.U.K.

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10.The manufacturer's obligations set out in points 7 and 9, may be fulfilled by his authorised representative, provided that they are specified in the mandate.U.K.