BEUDAMED
    59 results · 75ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR

    FDA Adverse Event
    Injury ·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015

    HS CATHETER, 5F

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·July 16, 2015

    J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR

    FDA Adverse Event
    Injury ·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015

    J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR

    FDA Adverse Event
    Injury ·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015

    UTERINE MANIPULATOR & INJECTOR (PUMI) 4.5MM

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·November 17, 2017

    CONNECTOR TUBING BX 100

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021

    CONNECTOR TUBING BX 100

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021

    CONNECTOR TUBING BX 100

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021

    CONNECTOR TUBING BX 100

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021

    UTERINE MANIPULATOR/INJECTOR

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·March 13, 2017

    CONNECTOR TUBING BX 100

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021

    ZANNANTI MANIPULATOR

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·November 28, 2016

    ZINNANTI MANIPULATOR

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·April 21, 2017

    PUMI

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC.·Product code LKF·May 1, 2017

    UTERINE MANIPULATOR / INJECTOR

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC·Product code LKF·May 3, 2017

    K-UMI MANIPULATOR, SIZE 5 MM, LENGTH 33CM

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC. (THOMAS MEDICAL)·Product code LKF·September 19, 2024

    UTERINE MANIPULATOR

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC. (THOMAS MEDICAL)·Product code LKF·September 28, 2017

    CANNULA, MANIPULATOR/INJECTOR, UTERINE

    FDA Adverse Event
    Malfunction ·CATHETER RESEARCH, INC./THOMAS MEDICAL INC.·Product code LKF·September 12, 2017

    ZANNANTI MANIPULATOR

    FDA Adverse Event
    Injury ·CATHETER RESEARCH INC DBA THOMAS MEDICAL INC·Product code LKF·December 20, 2011

    HS CATHETER, 5F

    FDA Adverse Event
    Injury ·CATHETER RESEARCH, INC. DBA THOMAS MEDICAL INC·Product code DRA·April 9, 2015