BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6000026-1999-00018

    MDR report key: 257890 · Received December 23, 1999

    Report

    Report Number
    6000026-1999-00018
    Event Type
    Malfunction
    Date Received
    December 23, 1999
    Date of Event
    November 24, 1999
    Report Date
    December 1, 1999
    Product Problem
    Yes
    Report Source
    Manufacturer report

    Patients

    Seq Age Sex Outcome Treatment
    1 Other