BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1223688-2000-00027

    MDR report key: 298422 · Received September 27, 2000

    Report

    Report Number
    1223688-2000-00027
    Event Type
    Injury
    Date Received
    September 27, 2000
    Date of Event
    August 21, 2000
    Product Code
    FDI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FDI 61 000977 88CK0349

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R