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

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    NEOCUSSOR (MASSAGER, BATTERY) POWERED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169139824·TRAY 1855129 CDHS SAS IMPLNT-INSTR EU

    MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN

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

    4010 NON CONDUCTIVE VENTILATOR CIRCUIT W/BACTERIAL

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 9, 2014

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·December 3, 2012

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·September 30, 2010