BEUDAMED
    9 results · 43ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DYNESYS SET SCREWS

    FDA Adverse Event
    Malfunction ·U&I CORP.·Product code NQP·April 14, 2011

    OPTIMA ZS TRANSITION SCREW

    FDA Adverse Event
    Injury ·U&I CORP.·Product code MNI·December 30, 2014

    OPTIMA SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·U&I CORP.·Product code MNI·December 30, 2014

    PREFIX SPINAL SYSTEM

    FDA Adverse Event
    Injury ·U&I CORP.·Product code MNH·February 6, 2016

    PERFIX SPINAL SYSTEM

    FDA Adverse Event
    Injury ·U&I CORP.·Product code MNH·February 23, 2015

    OPTIMA SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·U&I CORP.·Product code KWQ·August 21, 2006

    POLY SCREW DRIVER

    FDA Adverse Event
    Injury ·U&I CORP.·Product code HXX·August 16, 2006

    OPTIMA 2.5MM HEX DRIVER

    FDA Adverse Event
    Malfunction ·U&I CORP., AMERICA·Product code HXX·December 22, 2003

    OPTIMA 4MM HEX DRIVER

    FDA Adverse Event
    Malfunction ·U&I CORP., AMERICA·Product code HXX·December 22, 2003