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

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    Filters FDA Adverse Event ×

    AQUADEX FLEXFLOW

    FDA Adverse Event
    Malfunction ·NUWELLIS INC.·Product code KDI·December 13, 2021

    AQUADEX SMARTFLOW

    FDA Adverse Event
    Injury ·NUWELLIS, INC.·Product code KDI·June 3, 2025

    AQUADEX SMARTFLOW

    FDA Adverse Event
    Injury ·NUWELLIS, INC·Product code KDI·June 3, 2025

    AQUADEX SMARTFLOW

    FDA Adverse Event
    Malfunction ·NUWELLIS, INC.·Product code KDI·June 3, 2025

    AQUADEX SMARTFLOW

    FDA Adverse Event
    Injury ·NUWELLIS, INC·Product code KDI·January 27, 2026

    AQUADEX SMARTFLOW

    FDA Adverse Event
    Injury ·NUWELLIS, INC.·Product code KDI·March 30, 2026

    BARD POWER MIDLINE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code PND·April 14, 2026