BEUDAMED
    FDA Adverse Event Summary report: N

    1043534-1997-00006

    MDR report key: 209247 · Received September 2, 1997

    Report

    Report Number
    1043534-1997-00006
    Date Received
    September 2, 1997
    Date of Event
    November 13, 1996
    Product Code
    JWH
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1