BEUDAMED
    6 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    HARTFORD TOTAL HIP SYSTEM (TRI-WEDGE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    B.G. COMPRESSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CO2 EASY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 12, 2014

    XMTR MMT-7703NA MINILINK GST1 17L REPL

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·October 11, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·December 12, 2012