BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DRIVER SHAFT, T6, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·September 25, 2025

    DRIVER SHAFT, T6, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·September 23, 2025

    DRIVER SHAFT, T6, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 19, 2025

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 28, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR...·Product code CBK·December 10, 2012

    ECHELON LINEAR CUTTER RELOAD

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 25, 2015