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

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    HOWMEDICA(R) MONO-TUBE(TM) EXTERNAL FIXATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    D-STAT-DRY HEMOSTATIC BANDAGE; D-STAT RADIAL HEMOSTATIC BANDAGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    SchurSign Tissue Marker

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

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·December 16, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 12, 2014