BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2242551-1996-00013

    MDR report key: 52382 · Received November 25, 1996

    Report

    Report Number
    2242551-1996-00013
    Event Type
    Injury
    Date Received
    November 25, 1996
    Date of Event
    October 22, 1996
    Product Code
    BYE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1