BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2250051-2008-00081

    MDR report key: 1011478 · Received February 8, 2008

    Report

    Report Number
    2250051-2008-00081
    Event Type
    Malfunction
    Date Received
    February 8, 2008
    Product Code
    ---
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    NO INVESTIGATION COULD BE PERFORMED. THE CUSTOMER TECHNICAL SERVICES COULD NOT RETRIEVE THE COMPUTER FILE FOR THIS PLATE ON THE USER'S SERVER BECAUSE THE USER HAD DELETED THE REPORT FROM THE FILE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1