BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    ARTERIAL BLOOD FILTER HOLDER MODEL NO. AF-HE

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    Lumify Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    XLTEK STIMULATOR PROBES, MODELS 105233, 105234, 105235, 105236, 105237 AND 105238

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·June 10, 2014

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 10, 2012

    ANTERIOR CERVICAL PLATE ASSEMBLY, 3-LEVEL, 051MM (TI-6AL-4V NITINOL)

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code KWQ·June 23, 2015