BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR17000846-000

    MDR report key: 6988692 · Received October 30, 2017

    Report

    Report Number
    COR17000846-000
    Event Type
    No answer provided
    Date Received
    October 30, 2017
    Report Date
    October 30, 2017
    Product Code
    RDV
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    765593 RDV

    Patients

    Seq Age Sex Outcome Treatment
    1