BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    GENERATORS, PULSE, MODELS 5988/5989

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    CINCH ANCHOR, MODEL 1194

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIATHLON PS X3 TIBIAL INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·April 30, 2014

    PROTÉGÉ ®RX TAPERED CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·EV3 INC.·Product code NIM·October 10, 2012

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·July 27, 2010