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FluAB

Influenza A+B Test allows for the rapid, qualitative detection of influenza type A and type B antigens directly from nasal swab, nasopharyngeal swab, nasal aspirate, and nasal wash specimens. The test is

intended for use as an aid in the rapid differential diagnosis of acute influenza type A and type B viral infections. The test is not intended to detect influenza C antigens. Negative results should be confirmed by cell

culture; they do not preclude influenza virus infection and should not be used as the sole basis for treatment or other management decisions. The test is intended for professional and laboratory use.


Sample type:

    Product Advantage:

    • High Detection accuracy
    • High cost performance
    • Quality assurance
    • Fast delivery

    MATERIALS

    Materials Provided

    Test devices Droppers Buffer Package insert

    Materials Required But Not Provided

    Specimen collection containers Lancets (for fingerstick whole blood only)

    Centrifuge Micropipette Timer

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    DIRECTIONS FOR USE

    1.This test is for in vitro diagnostic use only. Do not swallow.

    2.Discard after first use.The test cannot be reused.

    3.Do not use test kit beyond expiration date.

    4.Do not use the kit if the pouch is punctured or not well sealed.

    5.Keep out of the reach of children.

    6.Keep your hand dry and clean before and during testing.

    7.Do not use the product out of doors.

    8.The procedures should be followed precisely for accurate results.

    9.Do not disassemble the battery. The battery is not detachable or changeable.

    10.Please follow local regulations to discard used tests.

    11.This device meets the electromagnetic emissions requirement of EN61326.Its electromagnetic emission is therefor low.Interference from other electrically driven equipment is not expected. This test should not be used in close proximity to sources of strong electromagnetic radiation,e.g.mobile phone,as there may prevent the test from working correctly.To avoid electrostatic discharge,do not use the test in a very dry environment,especially one in which synthetic materials are present.

    Clinical

    Table 1-1: Lyher T est Kit - Influenza A

    Sensitivity: 96.6%       Specificity: 100%     Accuracy: 98.7%

    Table 1-2: Lyher T est Kit - Inluenza B

    Sensitivity: 96.0%       Specificity: 100%     Accuracy: 98.9%

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