BEUDAMED
    FDA Adverse Event Summary report: N

    APTIMA

    MDR report key: 3363980 · Received September 3, 2013

    Report

    Report Number
    3363980
    Date Received
    September 3, 2013
    Date of Event
    August 30, 2013
    Report Date
    September 3, 2013
    Manufacturer
    GEN-PROBE, INC.
    Product Code
    MKZ
    Report Source
    User Facility report
    Reporter Location
    IL, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    436533 APTIMA DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA MKZ GEN-PROBE, INC. * 610515A

    Patients

    Seq Age Sex Outcome Treatment
    1 *