BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2110898-1997-00019

    MDR report key: 105943 · Received July 15, 1997

    Report

    Report Number
    2110898-1997-00019
    Event Type
    Injury
    Date Received
    July 15, 1997
    Date of Event
    August 14, 1990
    Manufacturer
    3M COMPANY
    Product Code
    FTR
    Removal / Correction Number
    UNK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FTR 3M COMPANY UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *