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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medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation (Text with EEA relevance) (repealed)

EU Regulation No 2007/2006 · Adopted 22 December 2006 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

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(Text with EEA relevance) (repealed)

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Annotations to the whole text

Textual amendments

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Repealed by Commission Regulation (EU) No 142/2011 of 25 February 2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive Text with EEA relevance.

Contents

  1. 1Scope Repealed
  2. 2Definition Repealed
  3. 3Importation Repealed
  4. 4Checks, transport and labelling Repealed
  5. 5Use and dispatch Repealed
  6. 6Records on use and dispatch Repealed
  7. 7Control Repealed
  8. 8Amendment to Annexes VIII and X of Regulation (EC) No 1774/2002 Repealed
  9. 9Entry into force Repealed
  10. Signature
  11. Annex I: Conditions for the registration or approval of the plant of origin in accordance with point (b) of Article 3 Repealed
  12. 1The operator or owner of the plant or his representative shall: Repealed
  13. 2The 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. Repealed
  14. 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 reagents Repealed
  15. MODEL 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 Repealed
  16. Annex IIIAnnex III Repealed

1ScopeF1

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2DefinitionF1

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3ImportationF1

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4Checks, transport and labellingF1

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5Use and dispatchF1

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6Records on use and dispatchF1

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7ControlF1

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8Amendment to Annexes VIII and X of Regulation (EC) No 1774/2002F1

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9Entry into forceF1

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Signature

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1The operator or owner of the plant or his representative shall:F1

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2The 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.F1

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MODEL 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 IIIF1

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