BEUDAMED
    FDA Adverse Event Other Summary report: N

    SAFEPICO

    MDR report key: 2132586 · Received March 2, 2009

    Report

    Report Number
    1523456-2009-00001
    Event Type
    Other
    Date Received
    March 2, 2009
    Date of Event
    February 14, 2009
    Report Date
    February 18, 2009
    Manufacturer
    RADIOMETER MEDICAL
    Product Code
    JKA
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SAFEPICO SAFEPICO JKA RADIOMETER MEDICAL SAFEPICO WQ50

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other