
COMMISSION REGULATION (EC) No 2007/2006 of 22 December 2006 implementing Regulation (EC) No 1774/2002 of the European Parliament and of the Council as regards the importation and transit of certain intermediate products derived from Category 3 material intended for technical uses in medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation (Text with EEA relevance) (repealed) 

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Scope
Article 1 
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Definition
Article 2 
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Importation
Article 3 
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Checks, transport and labelling
Article 4 
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Use and dispatch
Article 5 
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Records on use and dispatch
Article 6 
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Control
Article 7 
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Amendment to Annexes VIII and X of Regulation (EC) No 1774/2002
Article 8 
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Entry into force
Article 9 
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ANNEX I
Conditions for the registration or approval of the plant of origin in accordance with point (b) of Article 3
1. The operator or owner of the plant or his representative shall: 

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2. The competent authority of the third country shall at regular intervals carry out inspections of and supervise the plants registered or approved in accordance with this Regulation. 

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ANNEX II
Model declaration for the importation from third countries and for the transit through the European Community of intermediate products to be used for medical devices, in vitro diagnostics and laboratory reagentsMODEL DECLARATION FOR INTERMEDIATE PRODUCTS TO BE USED FOR MEDICAL DEVICES, IN VITRO DIAGNOSTICS AND LABORATORY REAGENTS, FOR DISPATCH TO OR FOR TRANSIT THROUGH THE EUROPEAN COMMUNITY 

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ANNEX III

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