BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DRIVER SHAFT, T10 HEXALOBE, CANNULATED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·April 7, 2021

    DRIVER SHAFT, T10 HEXALOBE, CANNULATED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 12, 2023

    DRIVER SHAFT, T10 HEXALOBE, CANNULATED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 15, 2025

    DRV SFT,T8 HEXALOBE CANN,STR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 12, 2023

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 19, 2010

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 14, 2012