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

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    C900 X-RAY FILM PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    UROFLEX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    EQUINOXE REVERSE HUMERAL LINER

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·June 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 19, 2010