BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 561042 · Received September 2, 2003

    Report

    Report Number
    MW1033823
    Date Received
    September 2, 2003
    Date of Event
    March 28, 2003
    Manufacturer
    *
    Product Code
    CEJ
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    NO INFORMATION

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * TANNING BED CEJ * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *