You are here:

  1. Home
  2. NICE Guidance
  3. Conditions and diseases
  4. Infections
  5. COVID-19

FebriDx for C-reactive protein and myxovirus resistance protein A testing

  • Medtech innovation briefing
  • Reference number: MIB224
  • Published:  26 August 2020

Download (PDF)
  • Overview
  • Summary
  • The technology
  • Regulatory information
  • Equality considerations
  • Clinical and technical evidence
  • Expert comments
  • Expert commentators
  • Development of this briefing

Regulatory information

FebriDx was CE marked as an in vitro diagnostic device in September 2014. This was updated in October 2018.


Next page Equality considerations Previous page The technology
Back to top