BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    DIGI -FLOW

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PSA4000 EEG MONITOR WITH FRONTAL PSI

    FDA 510(k)
    FDA Class 2 ·Neurology

    DIGITAL PACIFIER THERMOMETER (MODEL NO.: TM-03)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 17, 2013

    SIGMA 300 SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·December 13, 2010

    ASSURITY DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 8, 2014