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

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    Filters FDA Adverse Event ×

    L9000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·August 30, 2011

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·November 14, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 29, 2013

    SHARP HOOK

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code GDG·October 20, 2014