BEUDAMED
    FDA Adverse Event Other Summary report: N

    COR16000208-000

    MDR report key: 5683010 · Received May 26, 2016

    Report

    Report Number
    COR16000208-000
    Event Type
    Other
    Date Received
    May 26, 2016
    Report Date
    May 23, 2016
    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
    335652 RCG

    Patients

    Seq Age Sex Outcome Treatment
    1