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medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation (Text with EEA relevance) (repealed)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

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medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation (Text with EEA relevance) (repealed)

## Introductory text

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(Text with EEA relevance) (repealed)
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## 1 Scope

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## 2 Definition

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## 3 Importation

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## 4 Checks, transport and labelling

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## 5 Use and dispatch

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## 6 Records on use and dispatch

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## 7 Control

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

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## 9 Entry into force

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## Signature

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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 reagents

## 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 III 

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Source: https://www.legislation.gov.uk/eur/2006/2007 (the official version)
Page: https://openlegislation.uk/eu-regulation-2006-2007
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.