BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR25000228-000

    MDR report key: 22056278 · Received May 20, 2025

    Report

    Report Number
    COR25000228-000
    Event Type
    No answer provided
    Date Received
    May 20, 2025
    Report Date
    May 20, 2025
    Product Code
    IZL
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2142442 IZL

    Patients

    Seq Age Sex Outcome Treatment
    1 NA