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

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    PERIPHERAL NERVE STIMULATOR, MODEL A-200

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Tranquil-L™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788221570·TLIF Trial 9x10x32

    EasyTouch

    FDA UDI
    MHC MEDICAL PRODUCTS, LLC·MHC18221571·

    RF TENT

    FDA 510(k)
    FDA Class 2 ·Radiology

    ECHO Photocoagulator

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·May 20, 2014

    HS ACE 36CM SCISSOR HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·December 3, 2007

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012