BEUDAMED
    5 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MODULAR LATERALIZED TAPERLOC FEMORAL POROUS COATED 12.5 X 145 MM STEM TYPE I TAP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·November 15, 2012

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDI·September 24, 2015

    1.1MM THREADED GUIDE WIRE 150MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FZX·May 9, 2013

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 19, 2014

    M2A MAGNUM MODULAR HEAD 54MM HEAD DIAMETER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 21, 2012