BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 294885 · Received September 8, 2000

    Report

    Report Number
    1319447-2000-00002
    Event Type
    Other
    Date Received
    September 8, 2000
    Date of Event
    July 28, 2000
    Product Code
    BYD
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1