BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    IMPACT, MODEL E-12

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

    PressON™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788203300·Distraction Screwdriver, Springless

    PENUMBRA COIL SYSTEM/PENUMBRA COIL 400

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEPLOYABLE OXYGEN CONCENTRATION SYSTEM (DOCS)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

    GREENLIGHT XPS LASER SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 11, 2015

    COVIDIEN

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KNT·May 15, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 6, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 30, 2010