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

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    Filters Regulation: Us FDA ×

    Bifurcated Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    YUWELL Finger Pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Intense Pulsed Light Equipment

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MAXPLUS EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·July 15, 2011

    LEAD MODEL 303

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·November 5, 2008

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013