BEUDAMED
    FDA Adverse Event Injury Summary report: N

    9681900-1997-00018

    MDR report key: 97438 · Received June 11, 1997

    Report

    Report Number
    9681900-1997-00018
    Event Type
    Injury
    Date Received
    June 11, 1997
    Date of Event
    April 1, 1996
    Product Code
    CAE
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    UNKNOWN

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *