BEUDAMED
    FDA Adverse Event Summary report: N

    FLO-LAB

    MDR report key: 2406085 · Received January 5, 2012

    Report

    Report Number
    2406085
    Date Received
    January 5, 2012
    Date of Event
    December 29, 2011
    Report Date
    January 5, 2012
    Manufacturer
    PARKS MEDICAL ELECTRONICS
    Product Code
    JAF
    Report Source
    User Facility report
    Reporter Location
    MD, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLO-LAB SYSTEM, ULTRASOUND, PULSE VOLUME RECORDER JAF PARKS MEDICAL ELECTRONICS 2100SX *

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR