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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    THERA-TRONIC THERAPEUTIC TREATMENT TABLE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    C-FLEX SYSTEM SINGLE USE DISPOSABLE INJECTOR, MODEL R-INJ-02

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    AccuLIF TL and PL Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    PULSAR MAX

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·October 4, 2010

    EXCEL 23KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, LTD.·Product code LFL·November 27, 2012