BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GLIDESCOPE COBALT AVL BATON 3-4

    MDR report key: 2972568 · Received February 15, 2013

    Report

    Report Number
    9615393-2013-00087
    Event Type
    Malfunction
    Date Received
    February 15, 2013
    Date of Event
    January 18, 2013
    Report Date
    January 18, 2013
    Manufacturer
    VERATHON MEDICAL (CANADA) ULC.
    Product Code
    CCW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION RESULTS PENDING ANALYSIS OF THE PRODUCT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE ADULT BATON DID NOT DISPLAY AN OUTPUT ON THE LED'S. THERE WERE NO LIGHTS. NO PATIENT INJURY WAS INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    69950 GLIDESCOPE COBALT AVL BATON 3-4 NONE CCW VERATHON MEDICAL (CANADA) ULC. 0570-0313

    Patients

    Seq Age Sex Outcome Treatment
    1