BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ASSY, PROBE, BLADDERSCAN BVI 9400/9600

    MDR report key: 2972556 · Received February 15, 2013

    Report

    Report Number
    3022472-2013-00058
    Event Type
    Malfunction
    Date Received
    February 15, 2013
    Date of Event
    January 18, 2013
    Report Date
    January 18, 2013
    Manufacturer
    VERATHON MEDICAL
    Product Code
    IYO
    PMA / PMN Number
    K071217
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE DEVICE DID NOT TURN ON. DURING TROUBLESHOOTING, THE CUSTOMER WAS ADVISED OF HOW TO HARD RESET AND TO TAKE THE BATTERY OUT AND WAIT BEFORE TO TURN IT ON. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    69685 ASSY, PROBE, BLADDERSCAN BVI 9400/9600 NONE IYO VERATHON MEDICAL 0570-0188

    Patients

    Seq Age Sex Outcome Treatment
    1