BEUDAMED
    FDA Adverse Event Other Summary report: N

    8031673-2000-00001

    MDR report key: 284744 · Received June 29, 2000

    Report

    Report Number
    8031673-2000-00001
    Event Type
    Other
    Date Received
    June 29, 2000
    Date of Event
    January 1, 2000
    Product Code
    JJC
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JJC AIA PA PSA & NEXIA ANALYZ. SEVERAL

    Patients

    Seq Age Sex Outcome Treatment
    1