BEUDAMED
    3 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·January 15, 2013

    DELTA VALVE, REGULAR, LEVEL 2.0

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·December 1, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE·Product code KDJ·July 7, 2014