BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VENFLON I 18GA 1.2 MM X 45MM

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FOZ·October 28, 2019

    BD VENFLON¿ IV CANNULA

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMI·October 21, 2019

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD .·Product code MCM·April 2, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE·Product code ITI·March 22, 2011

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·April 18, 2008

    ALINITY M RESP-4-PLEX AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

    ALINITY M RESP-4-PLEX AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

    ALINITY M RESP-4-PLEX AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

    ALINITY M RESP-4-PLEX AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025