BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR17000835-001

    MDR report key: 7072525 · Received November 30, 2017

    Report

    Report Number
    COR17000835-001
    Event Type
    No answer provided
    Date Received
    November 30, 2017
    Report Date
    November 28, 2017
    Product Code
    RCC
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    849054 RCC

    Patients

    Seq Age Sex Outcome Treatment
    1