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Division (Diagnostic) sensitivityF1

United Kingdom

Original text. Later amendments are not shown.

The probability that the device gives a positive result in the presence of the target marker.

Annotations

Textual amendments

F1

Substituted by Commission Decision of 27 November 2009 amending Decision 2002/364/EC on common technical specifications for in vitro diagnostic medical devices (notified under document C(2009) 9464) (Text with EEA relevance) (2009/886/EC).