BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    SUTURE REMOVAL KIT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169139831·TRAY 1855131 CDHS XTRA MAS IMP-INST EU

    4013 NON CONDUCTIVE ANESTH. CIRCUIT W/BREATH-BAG

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    CONDUCTIVE ADHESIVE POST-OP ELECTRODE-TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    EXTENSION SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·December 3, 2012

    OT VERIO IQ METER

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

    TI END CAP T25 STRDRV HINDFOOT

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·September 30, 2010