BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GOBED II

    FDA Adverse Event
    Malfunction ·FLEXTRONICS EMS CANADA·Product code FNL·January 21, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 27, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP/DRIVELINE

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·December 19, 2022

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·July 11, 2013

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP/DRIVELINE

    FDA Adverse Event
    Death ·HEARTWARE, INC.·Product code DSQ·December 19, 2022