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

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    Filters FDA Adverse Event ×

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 22, 2014

    TI PROXIMAL TIBIA LISS PLATE 9 HOLES/220MM-LEFT

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HRS·February 4, 2013

    UNKNOWN BIGLIANI/FLATOW SHOULDER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSD·December 22, 2010