BEUDAMED
    8 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-MAGNUM 42-50 TPR INSRT STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 12, 2017

    MLRY-HD POR FMRL 14X175MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·December 12, 2017

    M2A-MAGNUM RECAP CUP 56ODX50ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 14, 2018

    APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTW·April 18, 2014

    I-STAT PT/INR CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE, CANADA LTD.·Product code JPA·June 25, 2010

    M2A-RINGLOC ACETABULAR LINER 28MM X SIZE 24 10 DEGREE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 26, 2012

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 12, 2017

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 12, 2017