BEUDAMED
    9 results · 49ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MIVI Q CATHETER

    FDA Adverse Event
    Malfunction ·MIVI NEUROSCIENCE, INC.·Product code DQY·August 18, 2023

    MIVI Q CATHETER

    FDA Adverse Event
    Injury ·MIVI NEUROSCIENCE, INC.·Product code NRY·September 1, 2023

    MODEL Q6-69145

    FDA Adverse Event
    Injury ·MIVI NEUROSCIENCE, INC.·Product code DQY·June 27, 2019

    Q6 ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·MIVI NEUROSCIENCE, INC.·Product code DQY·April 11, 2019

    MIVI Q CATHETER

    FDA Adverse Event
    Malfunction ·MIVI NEUROSCIENCE, INC.·Product code DQY·January 16, 2023

    MIVI Q CATHETER

    FDA Adverse Event
    Malfunction ·MIVI NEUROSCIENCE, INC.·Product code DQY·May 15, 2023

    MIVI Q DISTAL ACCESS CATHETER

    FDA Adverse Event
    Injury ·MIVI NEUROSCIENCE, INC.·Product code DQY·November 9, 2022

    MIVI Q CATHETER

    FDA Adverse Event
    Injury ·MIVI NEUROSCIENCE, INC.·Product code NRY·October 13, 2023

    MIVI Q ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·MIVI NEUROSCIENCE, INC.·Product code DQY·January 26, 2022