BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1526350-1996-00030

    MDR report key: 145563 · Received September 30, 1996

    Report

    Report Number
    1526350-1996-00030
    Event Type
    Injury
    Date Received
    September 30, 1996
    Date of Event
    June 26, 1996
    Manufacturer
    ZIMMER PATIENT CARE DIVISION
    Product Code
    GCY
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GCY ZIMMER PATIENT CARE DIVISION NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1