BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183446-1999-00001

    MDR report key: 218669 · Received March 30, 1999

    Report

    Report Number
    2183446-1999-00001
    Event Type
    Injury
    Date Received
    March 30, 1999
    Date of Event
    March 3, 1999
    Product Code
    FAT
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1