BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1220894-2000-00002

    MDR report key: 280824 · Received May 24, 2000

    Report

    Report Number
    1220894-2000-00002
    Event Type
    Malfunction
    Date Received
    May 24, 2000
    Date of Event
    April 21, 2000
    Product Code
    FPA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1