BEUDAMED
    5 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    INJECTION GOLD PROBE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 5, 2008

    UNK - PDL IMPLANT

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MJO·August 18, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·July 3, 2013

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 8, 2015

    REAGENT RED BLOOD CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·September 22, 2010