BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GYNECARE LAPAROSCOPIC MORCELLATOR

    MDR report key: 272774 · Received April 10, 2000

    Report

    Report Number
    2210968-2000-00068
    Event Type
    Injury
    Date Received
    April 10, 2000
    Date of Event
    March 9, 2000
    Manufacturer
    GYNECARE INNOVATION CENTER
    Product Code
    HFG
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GYNECARE LAPAROSCOPIC MORCELLATOR LAPAROSCOPIC MORCELLATOR HFG GYNECARE INNOVATION CENTER NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN