BEUDAMED
    9 results · 61ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    C4D (SP91)

    FDA Adverse Event
    Injury ·CELL MARQUE CORPORATION·Product code NJT·October 17, 2018

    KAPPA (EP171) RABBIT MONOCLONAL ANTIBODY

    FDA Adverse Event
    Malfunction ·CELL MARQUE CORPORATION·Product code NJT·July 31, 2019