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

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    MYOTONE EMG MONITOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SpheRx

    FDA UDI
    Nuvasive, Inc.·00887517063342·PPS Tulip, 6.25mm Rod Reduction

    Symmetry Polokoff

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482125854·Symmetry® Rasp, Polokoff, Double-Ended, 3 mm an...

    PICO 7 Single Use Negative Pressure Wound Therapy System

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

    RK EPIDURAL NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 25, 2014

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 2, 2012

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·September 18, 2007