BEUDAMED
    FDA Adverse Event Other Summary report: N

    C-SCAN

    MDR report key: 507425 · Received December 23, 2003

    Report

    Report Number
    8043485-2003-00002
    Event Type
    Other
    Date Received
    December 23, 2003
    Date of Event
    November 25, 2003
    Report Date
    November 27, 2003
    Manufacturer
    ESAOTE S.P.A.
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 C-SCAN MAGNETIC RESONANCE IMAGING DEVICE LNH ESAOTE S.P.A. 9700013002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other