BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    8013650

    FDA Adverse Event
    Malfunction ·October 29, 2018

    THORATEC IVAD

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·March 20, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·March 10, 2011

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·March 14, 2008

    VERSA-DIAL SHOULDER SYSTEM MODULAR HEAD W/VARIABLE OFFSET

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017

    VERSA-DIAL SHOULDER SYSTEM COMPREHENSIVE STANDARD ADAPTOR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017

    VERSA-DIAL SHOULDER SYSTEM MODULAR HEAD WITH VARIABLE OFFSET

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017

    VERSA-DIAL SHOULDER SYSTEM COMPREHENSIVE STANDARD ADAPTOR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·April 28, 2017