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

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    AORTIC ROOT CANNULA W/INTEGRAL PRESS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FREE GLIDING SLIPPED CAPITAL FEMORAL EPIPHYSIS SCREW (SCFE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER-FREE NITRILE PATIENT EXAMINATION GLOVE, WHITE (NON-COLORED), BLUE AND GREEN COLORED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BRYAN DUMON SILICONE STENT

    FDA Adverse Event
    Malfunction ·LYMOL MEDICAL CORPORATION·Product code NWA·October 28, 2019

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·May 26, 2014

    OMEGA¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·November 14, 2012

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·June 10, 2015