BEUDAMED
    FDA Adverse Event Other Summary report: N

    COR16000180-000

    MDR report key: 5640840 · Received May 9, 2016

    Report

    Report Number
    COR16000180-000
    Event Type
    Other
    Date Received
    May 9, 2016
    Report Date
    May 5, 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
    294421 RCG

    Patients

    Seq Age Sex Outcome Treatment
    1