BEUDAMED
    16 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

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    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025

    INSET I

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 12, 2025

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    COULTER ISOTON III DILUENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GIF·May 1, 2014

    COULTER ISOTON III DILUENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GIF·April 28, 2014

    COULTER ISOTON III DILUENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GIF·March 27, 2014