BEUDAMED
    738 results · 65ms · 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 ×

    PRESTILIX 1600XX

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KXJ·February 13, 2012

    AMX

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS MONTERREY MEXICO, S.A. DE C.V.·Product code IZL·May 5, 2026

    VMX MOBILE X-RAY SYSTEM

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZL·February 13, 2012

    AMX

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZL·March 3, 2026

    HORIZON LX 1.5T

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code LNH·December 12, 2016

    GE INNOVA 3100

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZI·November 14, 2016

    SIGNA OPENSPEED

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code LNH·January 11, 2012

    SIGNA 3.0T MR750

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code LNH·March 8, 2012

    REVOLUTION XR/D

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAA·March 8, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·March 20, 2012

    DISCOVERY XR650

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·March 13, 2012

    PRESTIGE SI

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAA·February 23, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·January 10, 2012

    DISCOVERY XR650

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·March 28, 2012

    DISCOVERY XR650

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC.·Product code KPR·February 20, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·February 1, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·February 1, 2012

    DISCOVERY MR750W 3.0T

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code LNH·January 11, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·February 20, 2012

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·February 2, 2012