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

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    MAX-I-PROBE HANDPIECE

    FDA 510(k)
    FDA Class 1 ·Dental

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209123148·

    FAMILY OF SELECTA OPHTHALMIC LASER SYSTEMS (SELECTA 1064, SELECTA SLT, SELECTA DUO), DELIVERY DEVICE AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Luggie Super

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UNKNOWN HIP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·June 5, 2014

    COMMUNICATOR

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code LWS·October 4, 2010

    6.0MM TI SELF-DRILLING SCHANZ SCREW 80MM THRD/200MM

    FDA Adverse Event
    Injury ·SYNTHES·Product code HWC·November 29, 2012