BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 917532 · Received March 23, 2007

    Report

    Report Number
    2954730-2007-00137
    Event Type
    Malfunction
    Date Received
    March 23, 2007
    Date of Event
    March 19, 2007
    Report Date
    March 22, 2007
    Manufacturer
    HEMOSENSE, INC.
    Product Code
    JPA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INRATIO PRECISION DATE PROVIDED BY END-USER LOT #060452/020685: FIRST TEST INR = 7.2, SECOND TEST INR = 6.4; THIRD TEST INR = 4.8 MEAN = 6.13; SD = 1.22; %CV = 19.9%. THE %CV IS LESS THAN OR EQUAL TO 20%. PER INTERNAL PROCEDURE, THE PRECISION PASSES THE CRITERIA FOR PRECISION. THE TEST IS CONSIDERED PRECISE AND NO FURTHER TESTING IS REQUIRED AT THIS TIME.

    Description of Event or Problem · 1

    CALLER ALLEGED IMPRECISION WITH INRATIO. RESULTS AS FOLLOWS: FIRST INR = 7.2, SECOND TEST INR = 6.4; THIRD TEST INR = 4.8.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST JPA HEMOSENSE, INC. * 060452

    Patients

    Seq Age Sex Outcome Treatment
    1 *