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

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    ENZYME LINEARITY CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    2.4MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036088873·2.7X18MM HIGH TORQUE CROSS-DRIVE SCREW

    MODIFICATION TO COROMETRICS MODEL 120IS MATERNAL/FETAL MONITORING SYSTEM.

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NUVASIVE NVM5 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ECHOTIP ULTRA ENDOBRONCHIAL ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·December 19, 2013

    SEVEN CONTINUOUS GLUCOSE MONITORING SENSOR

    FDA Adverse Event
    Other ·DEXCOM, INC.·Product code MDS·October 28, 2010

    ON-Q PAIN PUMP

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code MEB·January 8, 2013

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·July 3, 2014

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·April 15, 2019

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·April 15, 2019