BEUDAMED
    11 results · 73ms · Sources: EU EUDAMED, US FDA

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    FRESENIUS

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE AG·Product code KDL·February 25, 2002

    ULTRAFLUX AV 1000 S

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH·Product code KDI·May 6, 2022

    ULTRAFLUX AV 1000 S

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH·Product code KDI·May 6, 2022

    ULTRAFLUX AV 1000 S

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH·Product code KDI·May 6, 2022

    ULTRAFLUX AV 600 S

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH·Product code KDI·February 11, 2022

    MEDOS HILITE 7000 LT OXYGENATOR

    FDA Adverse Event
    Injury ·OGDEN MANUFACTURING PLANT·Product code DTZ·June 12, 2020

    FRESENIUS NOVALUNG NOVALUNG DEVICE FOR ECMO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE/XENIOS AG·Product code QJZ·January 31, 2025

    NOVALUNG SYSTEM FOR ECMO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE/XENIOS AG·Product code DWF·January 31, 2025

    NOVALUNG SYSTEM FOR ECMO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE/XENIOS AG·Product code QJZ·January 31, 2025

    XLUNG

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE/ XENIOS AG·Product code QJZ·January 21, 2025

    NOVALUNG SYSTEM FOR ECMO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE/XENIOS AG·Product code QJZ·January 31, 2025