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

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    Filters Status: Malfunction ×

    FLOSEAL ENDOSCOPIC APPLICATOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code LMF·July 17, 2008

    ACTIVA PC+S

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·November 9, 2018

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 29, 2018

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·March 5, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·February 3, 2011

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·April 13, 2018

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MBX·February 19, 2019