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Commission Directive 2006/17/EC of 8 February 2006 implementing Directive 2004/23/EC of the European Parliament and of the Council as regards certain technical requirements for the donation, procurement and testing of human tissues and cells (Text with EEA relevance)
Annex IV
Division 1
Division 1.3

Division 1.3.10

United Kingdom

Original text. Later amendments are not shown.

Wherever possible, only CE marked medical devices must be used and all concerned staff must have received appropriate training on the use of such devices.

← Division 1.3.9

Division 1.3.10

Division 1.4 →

Legislation: Commission Directive 2006/17/EC of 8 February 2006 implementing Directive 2004/23/EC of the European Parliament and of the Council as regards certain technical requirements for the donation, procurement and testing of human tissues and cells (Text with EEA relevance)
Citation: EU Directive 2006/17, division 1.3.10
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright
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