BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    STERI-TAMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROSTHETIC CEMENT REMOVER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLORECTAL CANCER RISK DETECTOR (TM)

    FDA 510(k)
    FDA Class 2 ·Hematology

    ENDO GIA UNIVERSAL 12 MM SINGLE USE INST

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·February 12, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 1, 2014