BEUDAMED
    11 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 12, 2021

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    Y-PLATE, 1.6MM, 6 HOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·June 14, 2021

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 11, 2024

    DRIVER SHAFT, T4, NON-RETAINING, MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 20, 2022

    DRIVER SHAFT, T4, NON-RETAINING, MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 3, 2024

    VA LOCKING SCREW, 1.4X8MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·July 3, 2024

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 3, 2024

    MONOPOLAR CURVED SCISSORSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 12, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 15, 2010

    DRIVER SHAFT, T4, NON-RETAINING, MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 8, 2021