BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IMPLANT: HA, SPLINE, 13MM, 3.25

    FDA Adverse Event
    Injury ·SULZER CALCITEK INC.·Product code DZE·May 22, 1997

    FR3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 19, 2014

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 7, 2011