BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR17000901-000

    MDR report key: 7050397 · Received November 21, 2017

    Report

    Report Number
    COR17000901-000
    Event Type
    No answer provided
    Date Received
    November 21, 2017
    Report Date
    November 20, 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
    826955 RCC

    Patients

    Seq Age Sex Outcome Treatment
    1