BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    E350I ELECTROCARDIOGRAPH

    FDA 510(k)

    TORQUE DEVICE FOR A GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOOD, OPERATING, SURGICAL

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

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 17, 2024

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·November 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2012