BEUDAMED
    FDA Adverse Event Other Summary report: N

    2250051-2000-00509

    MDR report key: 296279 · Received September 11, 2000

    Report

    Report Number
    2250051-2000-00509
    Event Type
    Other
    Date Received
    September 11, 2000
    Date of Event
    August 8, 2000
    Product Code
    JTC
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JTC

    Patients

    Seq Age Sex Outcome Treatment
    1