BEUDAMED
    3 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    S4 IMPLANTS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·April 21, 2008

    EVOLUT FX PLUS VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 14, 2025