BEUDAMED
    FDA Adverse Event Other Summary report: N

    8010168-1999-00001

    MDR report key: 227765 · Received June 9, 1999

    Report

    Report Number
    8010168-1999-00001
    Event Type
    Other
    Date Received
    June 9, 1999
    Date of Event
    April 16, 1999
    Product Code
    HDA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1