BEUDAMED
    20 results · 62ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    HS CATHETER, 5F

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

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·April 7, 2022

    ROSCH-UCHIDA TRANSJUGULAR LIVER ACCESS SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·September 21, 2021

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·May 19, 2021

    ZILVER VENA VENOUS SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code QAN·October 13, 2021

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 29, 2022