BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR21000137-000

    MDR report key: 11799374 · Received May 10, 2021

    Report

    Report Number
    COR21000137-000
    Event Type
    No answer provided
    Date Received
    May 10, 2021
    Report Date
    May 7, 2021
    Product Code
    KPR
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    691933 KPR

    Patients

    Seq Age Sex Outcome Treatment
    1