BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1003071 · Received January 31, 2008

    Report

    Report Number
    2250051-2008-00070
    Event Type
    Malfunction
    Date Received
    January 31, 2008
    Product Code
    JTC
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    NO INVESTIGATION COULD BE PEFORMED. 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 * JTC

    Patients

    Seq Age Sex Outcome Treatment
    1