BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    USA ELITE/USA SERIES DISPOSABLE ACTIVE CORD

    MDR report key: 275027 · Received April 18, 2000

    Report

    Report Number
    1519132-2000-00019
    Event Type
    Malfunction
    Date Received
    April 18, 2000
    Date of Event
    March 10, 2000
    Report Date
    April 18, 2000
    Manufacturer
    CIRCON ACMI
    Product Code
    FFZ
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 USA ELITE/USA SERIES DISPOSABLE ACTIVE CORD ACTIVE CORD FFZ CIRCON ACMI GDAC CC (3/99)

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO