BEUDAMED
    10 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GORE® CARDIOFORM SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MLV·July 12, 2023

    OPTOMONITOR 3

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·April 19, 2024

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·January 20, 2017

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·June 11, 2019

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·June 10, 2019

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·June 10, 2019

    OPTOWIRE

    FDA Adverse Event
    Malfunction ·OPSENS INC·Product code DQX·January 24, 2023

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·November 18, 2016

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·October 25, 2016

    SAVVYWIRE

    FDA Adverse Event
    Death ·OPSENS INC.·Product code DQX·March 28, 2025