BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·April 26, 2011

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·July 3, 2019

    COMP RVRS SHDR GLEN BSPLT +HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·July 3, 2019

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·March 15, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 8, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·April 26, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·April 26, 2011

    COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·August 13, 2018

    VERSA-DIAL/COMPREHENSIVE TI STANDARD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·August 13, 2018

    COMPREHENSIVE REVERSE HUMERAL TI TRAY 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·August 13, 2018

    M2A ACETABULAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 23, 2018