BEUDAMED
    FDA Adverse Event Other Summary report: N

    INTELECT

    MDR report key: 1012373 · Received March 7, 2008

    Report

    Report Number
    1022819-2008-00080
    Event Type
    Other
    Date Received
    March 7, 2008
    Date of Event
    February 20, 2008
    Report Date
    March 6, 2008
    Manufacturer
    CHATTANOOGA GROUP
    Product Code
    IPF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    AWAITING RETURN AND EVAL OF THE DEVICE.

    Description of Event or Problem · 1

    PT REPORTED SHOCKING SENSATION DURING ELECTROTHERAPY TREATMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTELECT POWER MUSCLE STIMULATOR IPF CHATTANOOGA GROUP INT002

    Patients

    Seq Age Sex Outcome Treatment
    1 Other