BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2132280-2001-00004

    MDR report key: 352435 · Received September 19, 2001

    Report

    Report Number
    2132280-2001-00004
    Event Type
    Injury
    Date Received
    September 19, 2001
    Date of Event
    August 4, 2001
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    42720 FSA

    Patients

    Seq Age Sex Outcome Treatment
    1