BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6000023-1999-00073

    MDR report key: 265922 · Received November 12, 1999

    Report

    Report Number
    6000023-1999-00073
    Event Type
    Malfunction
    Date Received
    November 12, 1999
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    DEVICED TESTED OUT OF SPECIFICATION DURING MFGR'S ANALYSIS.

    Patients

    Seq Age Sex Outcome Treatment
    1 000 Other