Detection Kit for Monkeypox Virus ( Real-time PCR )

Detection Kit for Monkeypox Virus ( Real-time PCR ) is designed for the qualitative detection of Monkeypox Virus (MPV) DNA extracted from skin, fluid, or crusts collected directly from skin lesions. It's based on real-time PCR technology, the primers and probes target specific sequences of MPV, and do not react with nucleic acids of other pathogens.

MPV Ag Rapid Test

The MPV Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of Monkeypox Virus (MPV) Antigen in human serum, oropharyngeal, skin lesion samples (skin surface and / or exudate swabs).

MPV IgG/IgM Rapid Test

The MPV IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of IgM and IgG antibodies to Monkeypox Virus (MPV) in human serum, plasma, venous whole blood, or fingertip blood. It is intended for use as an aid in identifying individuals with an adaptive immune response to MPV, indicating recent or prior infection. At this time, it is unknown how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The MPV IgG/IgM Rapid Test should not be used to diagnose acute MPV infection. For professional in vitro diagnostic use only.

Affinity A1c Analyzer

Affinity A1c Analyzer is a quantitative detection system based on boronate affinity chromatography, which is used with glycohemoglobin test kit to detect the level of hemoglobin A1c (HbA1c) in human whole blood (venous blood/finger prick).

SARS-CoV-2 IgG/IgM Rapid Qualitative Test

The Biotime SARS-CoV-2 IgG/IgM Rapid Qualitative Test is intended to qualify the SARS-CoV-2 IgG and IgM antibody in human plasma, serum or whole blood by colloidal gold immunochromatography assay. The test can be used as an aid detection to SARS-CoV-2 infection and thus caused COVID-19 disease.

CCP Rapid Quantitative Test (Fluorescence Immunoassay)

The Biotime CCP Rapid Quantitative Test is intended to quantify the concentration of CCP in human serum, plasma and whole blood on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of rheumatoid arthritis. -Fluorescence immunoassay -Rheumatoid arthritis For in vitro diagnostic use only. For professional use only.

ASO Rapid Quantitative Test (Fluorescence Immunoassay)

The Biotime ASO Rapid Quantitative Test is intended to quantify the concentration of ASO in human serum, plasma and whole blood onBiotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of auxiliary diagnosis of acute rheumatic fever. -Fluorescence immunoassay -Auxiliary diagnosis of acute rheumatic fever For in vitro diagnostic use only. For professional use only.

FLI-600 FIA Immunoassay Analyzer

FLI-600 is a fluorescent immunoassay system with 6 channels that uses blood and urine to measure the quantitative concentration of targeted analyte. Its automated test process enables to carry out multiple simultaneous tests for six different samples.

CMV IgG/IgM Rapid Test (Fluorescence Immunoassay)

TheCMV IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toCMV in human serum. IgG results with this assay are used to indicate past or recent infection with CMV. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recent CMV infections. CMV IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Cytomegalovirus (CMV) infection -For in vitro diagnostic use only. For professional use only.