BEUDAMED
    41 results · 39ms · Sources: EU EUDAMED, US FDA

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    UNI-VENT MODEL 73X

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOVEREIGN

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TORQUE INSTRUMENT, MODEL 8500

    FDA 510(k)
    FDA Unclassified ·Unknown

    COBALT HV BN CMT 40G-JAPAN

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LOD·July 29, 2016

    REFOBACIN PLUS BONE CEMENT 40

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L·Product code LOD·December 3, 2015

    REFOBACIN BONE CEMENT R 40X2 GERMAN

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L·Product code LOD·November 23, 2015

    OPTIPAC-S 40 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 22, 2016

    OPTIPAC-S 60 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

    OPTIPAC SOFTPAC HIPSET

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

    OPTIPAC-S 60 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

    OPTIPAC-S 60 REFOB BN CMT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

    OPTIPAC-S 40 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

    OPTIPAC-S 40 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

    OPTIPAC-S 80 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

    OPTIPAC-S 60 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 6, 2016

    OPTIPAC-S 40 REFOBACIN BONE CEMENT R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 7, 2016

    OPTIPAC-S 80 REFOBACIN PLUS BONE CEMENT

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 5, 2016

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 10, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·April 12, 2011

    CLINICAL INFORMATION CENTER

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code DSI·May 21, 2008