BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INDIANA TOME

    MDR report key: 173241 · Received June 17, 1998

    Report

    Report Number
    1825034-1998-00054
    Event Type
    Injury
    Date Received
    June 17, 1998
    Date of Event
    February 9, 1998
    Report Date
    June 17, 1998
    Manufacturer
    BIOMET, INC.
    Product Code
    EKD
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INDIANA TOME INSTRUMENT, MANUAL, SURGICAL EKD BIOMET, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other