BEUDAMED
    45 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK 2.0MM X 5MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    TMS SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/PK

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    2.0MM SYSTEM PLATE 4 HOLE PLATE, STRAIGHT, MEDIUM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    2.0MM SYSTEM PLATE DOUBLE-Y-SHAPE, LONG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·July 9, 2020

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·April 17, 2006

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·October 25, 2005

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DTB·January 25, 2005

    GUIDANT VASOVIEW 6 HARVESTING CANNULA

    FDA Adverse Event
    Injury ·GUIDANT CARDIAC SURGERY·Product code GEI·September 1, 2005

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 11, 2009

    TRIDENT CERAMIC ON CERAMIC HIP / HEMISPHERICAL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDIC CORK·Product code MEH·January 12, 2010

    INFUSE BONE GRAFT SMALL KIT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·June 11, 2009