BEUDAMED
    FDA Adverse Event Injury Summary report: N

    4173505

    MDR report key: 298308 · Received October 2, 2000

    Report

    Report Number
    1718873-2000-00011
    Event Type
    Injury
    Date Received
    October 2, 2000
    Date of Event
    September 11, 2000
    Report Date
    September 29, 2000
    Product Code
    FOS
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4173505 UVC, CATH SILICON, 35 FR, SL FOS NA 100029-1

    Patients

    Seq Age Sex Outcome Treatment
    1