BEUDAMED
    7 results · 64ms · 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 FDA Adverse Event ×

    MEVION S250I

    FDA Adverse Event
    Malfunction ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·November 4, 2020

    MEVION S250I

    FDA Adverse Event
    Malfunction ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·October 22, 2020

    MEVION S250I

    FDA Adverse Event
    Malfunction ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·May 22, 2024

    MEVION S250I

    FDA Adverse Event
    Malfunction ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·June 11, 2020

    MEVION S250I

    FDA Adverse Event
    Injury ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·February 1, 2024

    MEVION S250

    FDA Adverse Event
    Injury ·MEVION MEDICAL SYSTEMS, INC.·Product code LHN·January 13, 2017

    MEVION S250I PROTON THERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·MEVION MEDICAL SYSTEMS INC.·Product code LHN·January 15, 2025