BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    DRILL BIT, 1.7MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·August 12, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 2, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 8, 2025

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 4, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 5, 2025

    9900

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

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 15, 2010