BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2132280-1999-00001

    MDR report key: 221068 · Received April 16, 1999

    Report

    Report Number
    2132280-1999-00001
    Event Type
    Injury
    Date Received
    April 16, 1999
    Date of Event
    March 24, 1999
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FSA PC 350

    Patients

    Seq Age Sex Outcome Treatment
    1