BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EMERALD DIAGNOSTIC GUIDEWIRES

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DQX·March 8, 2013

    MITEK BIOINTRAFIX TAPERED SCREW, 6-8 MM X 30 MM

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HWC·August 8, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 16, 2011

    MENTOR MEMORYGEL XTRA BREAST IMPLANT

    FDA Adverse Event
    Malfunction ·MENTOR TEXAS·Product code FTR·August 21, 2025