BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    MAYO-HEGAR NEEDLE HOLDER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    LTM-LABAROSCOPIC SURGICAL MESH

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

    WARMER 2000LD

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 16, 2014

    PULSAR GENERATOR

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

    KEEPSAFE DELUXE NO POWER SWITCH

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·August 26, 2010