BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR23000012-000

    MDR report key: 16253851 · Received January 25, 2023

    Report

    Report Number
    COR23000012-000
    Event Type
    No answer provided
    Date Received
    January 25, 2023
    Report Date
    January 17, 2023
    Product Code
    RDW
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    377734 RDW

    Patients

    Seq Age Sex Outcome Treatment
    1 NA