BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1831750-1997-00020

    MDR report key: 141327 · Received December 30, 1997

    Report

    Report Number
    1831750-1997-00020
    Event Type
    Injury
    Date Received
    December 30, 1997
    Date of Event
    September 5, 1997
    Product Code
    FPO
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1