BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    LYOPLANT DURA SUBSTITUTE(VARIOUS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARTHROCARE SPINEWANDS

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

    Anterior Spine Truss System (STS) Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INDIGO 1.0CM LASER FIBER

    FDA Adverse Event
    Death ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 29, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 25, 2011