BEUDAMED
    6 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    "ACORN BUR, TOOLSTEEL, LONG"

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD·Product code HBE·November 19, 2009

    BARD TEGRESS URETHRAL BULKING AGENT

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code LNM·December 27, 2006

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·November 12, 2008

    VERSA DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·August 31, 2011

    FLORENCE DC W/REGULAR SIDERAIL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 16, 2013

    COBRA PZF

    FDA Adverse Event
    Injury ·CELONOVA BIOSCIENCES, INC.·Product code MAF·August 17, 2018