INTENDED USE

The AQ+ COVID-19 Ag Rapid Self-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.

The test is for self-test with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older with symptoms of COVID-19 within the first seven (7) days of symptom onset. Or self-test with adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first seven (7) days of symptom onset.

INTENDED USE

The Advanced Quality Rapid Anti-HIV (1&2) Test is a colloidal gold enhanced immunochromatographic assay for the qualitative detection of antibodies to human immunodeficiency virus (HIV) in human whole blood, serum or plasma from all groups (including neonates, pregnant women, etc). This is a screening test, and all positives must be confirmed using an alternative test such as western blot.

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

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.

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.