BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221923-2002-00001

    MDR report key: 377357 · Received February 6, 2002

    Report

    Report Number
    1221923-2002-00001
    Event Type
    Other
    Date Received
    February 6, 2002
    Date of Event
    January 8, 2002
    Product Code
    HIF
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1