BEUDAMED
    7 results · 15ms · 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 ×

    DRIVER SHAFT, T10, NON-RETAINING

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 17, 2024

    DRIVER SHAFT, T10, NON-RETAINING

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 8, 2023

    DRIVER SHAFT, T10, NON-RETAINING

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 7, 2024

    DRIVER SHAFT, T10, NON-RETAINING

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 13, 2026

    GALAXY INTRAVASCULAR ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (CE)·Product code IYO·December 19, 2012

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·October 13, 2010

    HAND PIECE FOR BATTERY POWERED DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 21, 2025