BEUDAMED
    10,000 results · 79ms · 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 ×

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·November 18, 2014

    ARTHREX INC.

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·December 27, 2003

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·September 28, 2011

    ARTHREX, INC

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FMI·December 29, 2011

    ARTHREX, INC

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GAB·December 29, 2011

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·ARTHREX INC.·Product code HRX·September 8, 2006

    ARTHREX, INC. SCORPION NEEDLE, KNEE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·January 2, 2024

    ARTHREX INC SCORPION MULTIFIRE NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX INC.·Product code GAB·September 13, 2018

    NANOSCOPE CONSOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 11, 2024

    NANOSCOPE CONSOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·April 24, 2024

    SHAVER HP, APSII, HAND CONTROL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·June 7, 2024

    DW OUTFLOW TUBE SET W/REDEUCE TUBING

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·June 6, 2024

    DRILL JACOBS CHUCK 0-4.0 MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 31, 2024

    ARTHREX AR-600,HANDPIECE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 30, 2024

    PIN DRIVER ATTACHMENT 1.0-2.4 MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 31, 2024

    ARTHREX AR-300,HANDPIECE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 31, 2024

    NANOSCOPE CONSOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·May 29, 2024

    WIRE DRIVER ATTACHMENT 0.6-1.6 MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 31, 2024

    BIO-COMP SWVLK 3.5X 15.8MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·April 10, 2024

    BIO-COMP SWVLK 3.5X 15.8MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·April 22, 2024