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

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    TENDERFOOT(R), MODIFICATION

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IMAGE1 GI CCU MODEL 22203020-114

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

    MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX

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

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·December 1, 2010

    ENERGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    EXPANDING HUMERAL INSERT TRIAL - SMALL 32MM STANDARD

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWS·July 3, 2014