BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1052997-1997-00001

    MDR report key: 98598 · Received June 14, 1997

    Report

    Report Number
    1052997-1997-00001
    Event Type
    Malfunction
    Date Received
    June 14, 1997
    Date of Event
    March 27, 1997
    Product Code
    FLE
    Removal / Correction Number
    1052997-19
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1