BEUDAMED
    FDA Adverse Event Other Summary report: N

    9681384-1997-00026

    MDR report key: 80629 · Received March 26, 1997

    Report

    Report Number
    9681384-1997-00026
    Event Type
    Other
    Date Received
    March 26, 1997
    Date of Event
    February 1, 1997
    Product Code
    FEG
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1