BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEGAR

    MDR report key: 234961 · Received July 29, 1999

    Report

    Report Number
    2431021-1999-00004
    Event Type
    Injury
    Date Received
    July 29, 1999
    Date of Event
    July 14, 1999
    Report Date
    July 29, 1999
    Manufacturer
    MILTEX INSTRUMENT CO. INC.
    Product Code
    HDQ
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEGAR UTERINE DILATOR HDQ MILTEX INSTRUMENT CO. INC. 30-530 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1