Division II Module B — EU-type examination
United Kingdom
- 1Division 1
- 2EU-type examination may be carried out in one of the following ways:
- 3The manufacturer shall lodge an application for EU-type examination with a single notified body of his choice.
- 4The notified body shall:
- 4.1examine the technical documentation and supporting evidence to assess the adequacy of the technical design of the interoperability constituent;
- 4.2Division 4.2
- 4.3Division 4.3
- 4.4Division 4.4
- 4.5Division 4.5
- 5Division 5
- 6Where the type meets the requirements of the specific legislative instrument that apply to the interoperability constituent concerned, the notified body shall issue an EU-type examination certificate to the manufacturer. The certificate shall contain the name and address of the manufacturer, the conclusions of the examination, the conditions (if any) for its validity and the necessary data for identification of the approved type. The certificate may have one or more annexes attached.
- 7The notified 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 the legislative instrument, and shall determine whether such changes require further investigation. If so, the notified body shall inform the manufacturer accordingly.
- 8Each notified body shall inform its notifying authorities concerning the EU-type examination certificates and/or any additions thereto which it has issued or withdrawn, and shall, periodically or upon request, make available to its notifying authorities the list of certificates and/or any additions thereto refused, suspended or otherwise restricted.
- 9Division 9
- 10Division 10
Notes on Division
Footnotes
- f1
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Decision No 768/2008/EC of the European Parliament and of the Council of 9 July 2008 on a common framework for the marketing of products and repealing Council Decision 93/465/EEC (Text with EEA relevance).