BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2647856-2000-00017

    MDR report key: 278161 · Received May 16, 2000

    Report

    Report Number
    2647856-2000-00017
    Event Type
    Injury
    Date Received
    May 16, 2000
    Date of Event
    February 24, 2000
    Product Code
    FGD
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FGD

    Patients

    Seq Age Sex Outcome Treatment
    1