BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR26000112-000

    MDR report key: 25068755 · Received May 4, 2026

    Report

    Report Number
    COR26000112-000
    Event Type
    No answer provided
    Date Received
    May 4, 2026
    Report Date
    May 4, 2026
    Product Code
    IZO
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    148486 IZO

    Patients

    Seq Age Sex Outcome Treatment
    1 NA