BEUDAMED
    8 results · 107ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HYDROFINITY HYDROPHILLIC GUIDE WIRE

    FDA Adverse Event
    Malfunction ·NITINOL DEVICES AND COMPONENTS INC·Product code DQX·March 12, 2014

    GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·June 5, 2023

    IMPL SYS,CMC MINI T-ROPE,1.1 MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTN·March 21, 2024

    ABRE VENOUS SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code QAN·April 1, 2026

    BANANA SUTURELASSO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 20, 2024

    RIA DRIVESHAFT L520

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·March 30, 2018

    RIA DRIVESHAFT L520

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·March 30, 2018

    DRIVE SHAFT FOR RIA 2 520MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·September 16, 2021