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

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    Axis Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Proxis Ureteral Access Sheath

    FDA UDI
    C. R. Bard, Inc.·00801741212765·Proxis Ureteral Access Sheath

    TIBIAL NAIL, STANDARD T2 TIBIA 9X300 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 12, 2012

    ESTYLUS ELECTRIC MOTOR SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    PROINSERT

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 20, 2025

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR IRELAND·Product code MIH·August 26, 2011

    PLUM XLMD PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 30, 2008

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 17, 2013