BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 584888 · Received March 21, 2005

    Report

    Report Number
    2248721-2005-00001
    Event Type
    Other
    Date Received
    March 21, 2005
    Date of Event
    February 10, 2005
    Manufacturer
    INTERNATIONAL TECHNIDYNE CORP.
    Product Code
    JPA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * JPA INTERNATIONAL TECHNIDYNE CORP. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *