BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    COR17000414-000

    MDR report key: 6569234 · Received May 16, 2017

    Report

    Report Number
    COR17000414-000
    Event Type
    No answer provided
    Date Received
    May 16, 2017
    Report Date
    May 12, 2017
    Product Code
    RCG
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER
    Health Professional
    I

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    349520 RCG

    Patients

    Seq Age Sex Outcome Treatment
    1