BEUDAMED
    93 results · 32ms · Sources: EU EUDAMED, US FDA

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    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

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·May 10, 2006

    RX ACCULINK CAROTID STENT SYSTEM

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

    SELOX ST 60

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.,·Product code LWS·December 2, 2005

    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

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·July 20, 2007

    NELLCOR N595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code DQA·October 27, 2005

    GUIDANT VASOVIEW 6 HARVESTING CANNULA

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

    ACTROS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.,·Product code DTB·September 19, 2005

    MARKED GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code DQX·March 3, 2008

    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