BEUDAMED
    5 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 9, 2014

    CONTAK RENEWAL 3

    FDA Adverse Event
    Death ·CLONMEL·Product code NIK·March 3, 2006

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 31, 2007

    OXF ANAT BRG LT SM SIZE 4 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·April 8, 2019

    OXF TWIN-PEG CMNTD FEM SM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·April 8, 2019