BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR22000217-000

    MDR report key: 15710170 · Received November 1, 2022

    Report

    Report Number
    COR22000217-000
    Event Type
    No answer provided
    Date Received
    November 1, 2022
    Report Date
    November 1, 2022
    Product Code
    IZL
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1103579 IZL

    Patients

    Seq Age Sex Outcome Treatment
    1