BEUDAMED
    11 results · 79ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CANON AQUILION PRIME

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·June 22, 2021

    CANON AQUILION PRIME

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·June 22, 2021

    RADPRO MOBILE X-RAY SYSTEM

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code IZL·December 17, 2020

    CANON AQUILION ONE

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·November 16, 2022

    CANON AQUILION ONE

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·November 16, 2022

    CANON AQUILION ONE

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·November 16, 2022

    CANON CT SCANNER

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEMS USA, INC.·Product code JAK·November 30, 2018

    RADPRO

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEMS USA, INC.·Product code IZL·September 23, 2021

    AQUILION

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEMS USA, INC.·Product code JAK·January 19, 2018

    TOSHIBA-CANON INFINIX- 1

    FDA Adverse Event
    Injury ·TOSHIBA-CANON MEDICAL SYSTEMS USA, INC.·Product code JAA·December 6, 2018

    ARTIC SUN 5000, 115V NA

    FDA Adverse Event
    Injury ·DYMAX CORP. -2523003·Product code DWJ·July 7, 2017