BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CASE IV

    MDR report key: 253628 · Received December 10, 1999

    Report

    Report Number
    2118418-1999-00002
    Event Type
    Injury
    Date Received
    December 10, 1999
    Date of Event
    November 1, 1999
    Report Date
    December 10, 1999
    Manufacturer
    WR MEDICAL ELECTRONICS
    Product Code
    LLN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THERMAL STIMULATOR NO GOOD. BURNED DR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CASE IV COMPUTER AIDED SENSORY EVALUATOR LLN WR MEDICAL ELECTRONICS IV *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention