OpenLegislation

Division 1.2 Assessment procedureF1

United Kingdom Repealed

Original text. Later amendments are not shown.

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  1. 1.2.1Animals as a source of material
  2. 1.2.2Geographical sourcing
  3. 1.2.3Nature of starting tissue
  4. 1.2.4Inactivation or removal of transmissible agents
  5. 1.2.5Quantities of animal starting tissues or derivatives required to produce one unit of the medical device
  6. 1.2.6Tissues or derivatives of animal origin coming into contact with the patients and users
  7. 1.2.7Route of administration

Annotations

Textual amendments

F1

Repealed by Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin (Text with EEA relevance).