BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6000023-1999-00062

    MDR report key: 265478 · Received September 8, 1999

    Report

    Report Number
    6000023-1999-00062
    Event Type
    Malfunction
    Date Received
    September 8, 1999
    Date of Event
    February 22, 1999
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    TESTED OUT OF SPECIFICATIONS DURING MFGR'S ANALYSIS.

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other