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

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    Filters FDA Adverse Event ×

    VERSA-DIAL 42X18X46 HUMERAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 7, 2018

    PT HYBRID GLENOID POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 7, 2018

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 7, 2018

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 4, 2014

    INRATIO

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC·Product code GJS·November 26, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code DSK·September 27, 2010