BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    BARTELS RUBELLA IGM EIA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BECTON DICKINSON LOGIC BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    DELTA SHUNT KIT REGULAR, PL 1.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·November 19, 2010

    ANEURX ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·January 18, 2013

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 9, 2014

    AUROUS CENTIMETER VESSEL SIZING CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQO·July 20, 2017