BEUDAMED
    66 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VERSA-DIAL 46X18X53 HUMERAL HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·December 8, 2016

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·December 8, 2016

    COMPREHENSIVE SHOULDER SYSTEM STANDARD TAPER ADAPTOR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBF·December 8, 2016

    BD MICRO-FINE¿ IV INSULIN SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·December 26, 2018

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 14, 2024

    CRYSTALENS ACCOMODATING IOL

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code NAA·May 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 24, 2014

    LINOX S 65

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·May 24, 2011

    COMPREHENSIVE PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 24, 2017

    VERSA-DIAL/COMPREHENSIVE 46X18X53 HUMERAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·October 24, 2017

    SM HYBRID COMPREHENSIVE GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 24, 2017

    VERSA-DIAL/COMPREHENSIVE TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·October 24, 2017

    COMPREHENSIVE VERSA-DIAL HUMERAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·May 29, 2018

    CR PROLONG 36MM BRNG STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 31, 2022

    SM HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 9, 2022

    UNKNOWN GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 30, 2024

    STANDARD 36MM DIAMETER BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 30, 2024

    BIO-MOD HUM HEAD 40DIAX15MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·November 9, 2022

    COMPR METAL IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PHX·April 8, 2026

    HYBRID ARCOM GLENOID BASE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·July 13, 2017