BEUDAMED
    4 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·June 5, 2014

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·November 29, 2012

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·June 17, 2015

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·September 30, 2022