BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VIDAS 30

    MDR report key: 926927 · Received August 24, 2004

    Report

    Report Number
    3002769706-2004-00012
    Event Type
    Malfunction
    Date Received
    August 24, 2004
    Date of Event
    August 10, 2004
    Report Date
    August 24, 2004
    Manufacturer
    BIOMERIEUX, INC.
    Product Code
    JZT
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VIDAS 30 IMMUNOFLUOROMETER EQUIPMENT JZT BIOMERIEUX, INC. VIDAS 30 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA