BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2183613-2010-00022

    MDR report key: 2377005 · Received December 15, 2011

    Report

    Report Number
    2183613-2010-00022
    Event Type
    Malfunction
    Date Received
    December 15, 2011
    Date of Event
    November 13, 2009
    Report Date
    November 25, 2024
    Manufacturer
    MEDTRONIC MILACA, INC.
    PMA / PMN Number
    P820003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    BIOMEDICAL ENGINEER
    Health Professional
    Yes

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown