BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 3606807 · Received August 28, 2013

    Report

    Report Number
    3606807
    Date Received
    August 28, 2013
    Date of Event
    August 22, 2013
    Report Date
    August 27, 2013
    Manufacturer
    LIFE INSTRUMENT CORP.
    Product Code
    HAE
    Report Source
    User Facility report
    Reporter Location
    MA, US

    Narratives

    Description of Event or Problem · 1

    PITUITARY BROKE IN PATIENT'S LUMBAR SPINE ALL PIECES WERE RETRIEVED AND VERIFIED BY THE SURGEON AND BY X-RAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    424787 * RONGEURS HAE LIFE INSTRUMENT CORP. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR