BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 74949 · Received February 27, 1997

    Report

    Report Number
    2024170-1997-00007
    Event Type
    Malfunction
    Date Received
    February 27, 1997
    Date of Event
    February 1, 1997
    Product Code
    LSZ
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    CORRECTED DATA: THIS REPORT IS SUBMITTED TO CORRECT THE MFG# REPORT NUMBER TO READ "2024170-1997-00007". THIS REPORT WAS INITIALLY SUBMITTED WITH REPORT# "2124170-1997-00007", WHICH IS INCORRECT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1