BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    INSTRUMENTARIUM MEGA4, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377069054·RELINE C Screw, 4.5x28mm MA

    Solstice Occipito-Cervico-Thoracic System

    FDA UDI
    Life Spine, Inc.·00190837014773·

    MODEL 8806 SD SUNGLASSES W/ACRYLIC LENSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    BIOCLOT C KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    INTERLOCKING DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRD·November 22, 2010

    INCEPTA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 4, 2012