BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    HANDPIECE, LIFT, ENDO

    FDA 510(k)
    FDA Class 1 ·Dental

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517199850·Archon Screw, 4.0x13mm Self-Drill Var

    Titanium TomoFix Medial High Tibia Plate Anatomical

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LENSES, CONTACT, POLYMETHYL METHACRYLATE

    FDA 510(k)
    FDA Unclassified ·Unknown

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·June 12, 2007

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 3, 2014

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012