Enabling TORCH screening at the point of care

Exclusive method

Solid-phase method

Accuracy rate: 100%

INTENDED USE

The kit is intended to qualitatively detect ABO blood group system A/B antigen and Rh blood group system D antigen in fresh finger prick blood/ anticoagulated venous whole blood.

Human blood contains a wide variety of blood groups, of which ABO and RhD are the most common. Blood group identification is a crucial test item prior to clinical blood transfusion, and has important clinical significance. When the blood group antigen on the surface of red blood cells comes in contact with the corresponding antibody, red blood cells will undergo agglutination reaction, which will eventually lead to hemolysis of red blood cells and endanger life. As a result, correct identification of ABO and RhD blood antigens is an essential prerequisite to ensure safe blood transfusion and avoid related diseases.

Ultra Sensitive

INTENDED USE

The AQ+ COVID-19 Ag Rapid Test is a colloidal gold enhanced, rapid immunochromatographic assay for qualitative detection of SARS-CoV-2 antigens in the nasopharyngeal/ nasal specimen collected by swabs from individuals who are suspected of having COVID-19. The test is used as an aid in the diagnosis of SARS-CoV-2 infection. The test is suitable for use under healthcare professional supervision. Individuals should have appropriate training in how to administer the test correctly. Remote healthcare professional supervision can be used with appropriate clinical governance, once training has been completed and verified.

﹒Sensitivity: 93.64%

﹒Specificity: 100.00%

﹒Specimen: Nasal specimen

﹒ISO13485

AQ⁺ HIV Ag/Ab Combo Rapid Test is an in vitro, qualitative immunoassay for the detection of Human Immunodeficiency Virus type 1 (HIV-1) antibody, type 2 (HIV-2) antibody and free HIV-1 p24 antigen in human whole blood (venous and fingertip), serum，plasma. It is intended for use as a point-of-care test to aid in the diagnosis of HIV infection.

INTENDED USE

The kit is intended to qualitatively detect Toxoplasma IgM, Toxoplasma IgG, Cytomegaloviru IgM, Cytomegaloviru IgG and Rubella virus IgG in human serum, plasma or whole blood in vitro. It is suitable for clinical auxiliary diagnosis of Toxoplasma infection, Cytomegalovirus infection and Rubella virus infection as well as their epidemiological inverstigation.

INTENDED USE

The AQ+ Rapid COVID-19/Flu Combo Test is a colloidal gold enhanced, rapid immunochromatographic assay for qualitative detection of antigens to SARS-CoV-2 and Influenza A and influenza B present in human nasopharyngeal/nasal specimens. The test is used as an aid in the diagnosis of COVID-19 infection and/or Influenza A and Influenza B.

INTENDED USE

The Rapid Dengue Duo (NS1 Ag & IgM/IgG Ab) Test is a colloidal gold enhanced, rapid immunochromatographic assay for the qualitative detection of both dengue virus NS1 Ag and IgM& IgG antibodies to dengue virus (DV) in human whole blood, serum or plasma, and serves as an aid in the diagnosis of Dengue infections. It only provides preliminary analysis results but not critical diagnosis criteria, the obtained results should be analyzed in connection with other clinical information, e.g. clinical symptoms, and using more specific alternative diagnosis methods to make final decision. This test is a screening test, and all positives must be confirmed using an alternate test. The test is intended for healthcare professional use only.