The HSV-2 IgG/IgM Rapid Test is an in vitro immunoassay for the qualitative determination of IgG and IgM class antibodies to HSV2 in human serum. The test is intended for use as an aid in the assessment of immune status and as an aid in the diagnosis of HSV infection. The HSV-2 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 -Herpes simplex viruses2 (HSV-2) infection -For in vitro diagnostic use only. For professional use only.

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.

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.

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.

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

The Biotime Helicobacter pylori (H.pylori) Antigen Rapid Test is intended to qualitatively detect the Helicobacter pylori (H.pylori) antigen in human faeces samples on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an early aid diagnosis and screening of  Helicobacter pylori infection. For in vitro diagnostic use only. For professional use only.

The BiotimeTSH/FT3/FT4Rapid Quantitative Test is intended to quantitatively detect the concentration of thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), and free thyroxine (FT4) in human serum and plasma samples on the Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an adjunctive diagnosis of thyroid function. For in vitro diagnostic use only. For professional use only.

The Biotime TSH/TT3/TT4Rapid Quantitative Testis intended to quantitatively detect theconcentration of thyroid stimulating hormone (TSH),total triiodothyronine (TT3) and total thyroxine (TT4) in human serum and plasma samples on Biotime FIA Analyzer byfluorescent immunoassay. The test is used as an aiddiagnosis of thyroiddisease. For in vitro diagnostic use only. For professional use only.