BEUDAMED
    4 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·HOUSTON·Product code LYJ·December 23, 2025

    ERBE VIO 300 D

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·March 4, 2022

    UNKNOWN KNEE

    FDA Adverse Event
    Death ·ZIMMER BIOMET, INC.·Product code HRY·July 9, 2015

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·December 29, 2022