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MR-proADM test for use with clinical deterioration scores in cases of suspected infection

Medtech innovation briefing [MIB195] Published: 11 October 2019

  • Overview
  • Summary
  • The technology
  • Regulatory information
  • Equality considerations
  • Clinical and technical evidence
  • Specialist commentator comments
  • Specialist commentators
  • Development of this briefing
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Regulatory information

Regulatory information

MR-proADM is a CE-marked in vitro diagnostic device.


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