Analizador CLIA CLI-1600

TheRubella IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toRubella in human serum.IgG results with this assay are used to indicate past or recent infection withRubella. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recent Rubella infections. Rubella 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.

D-Dimer Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the D-Dimer concentration in human sodium citrate anticoagulant-contained plasma (1:9) and venous whole blood samples, mainly used for auxiliary diagnosis of cardiac diseases.

CK-MB Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Creatine kinase-MB (CK-MB) concentration in human serum, plasma that contains heparin /EDTA and other anticoagulants and venous whole blood samples, mainly used for auxiliary diagnosis of cardiac diseases.

HbA1c Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Glycated hemoglobin A1c (HbA1c) concentration in human whole blood that contains EDTA or without anticoagulants samples, mainly used for the supervising of long-term glycemic control in diabetic individuals and auxiliary diagnosis of diabetes and identify patients at risk of diabetes.

TheToxoplasma IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toToxoplasma gondii in human serum.IgG results with this assay are used to indicate past or recent infection withToxoplasma gondii. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recentToxoplasma gondii infections. Toxoplasma 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 -Toxoplasma gondii infection -For in vitro diagnostic use only. For professional use only.

Biotime 2 en 1 El kit de prueba puede ayudar al operador a distinguir la infección bacteriana y la infección viral, y mejorar la precisión del diagnóstico clínico de enfermedades infecciosas.

El analizador hba1c totalmente automatizado HLC-100 de biotime brinda una solución rápida, confiable para el diagnóstico de diabetes. utiliza la técnica analítica de cromatografía líquida de alto rendimiento (HPLC), un estándar de oro que ayuda a detectar la hemoglobina glicosilada (hba1c) con una calidad superior precisión. su capacidad para medir hba1c, hbf, y otros fragmentos de hemoglobina permite a los médicos realizar diagnósticos rápidos, precisos,, lo que facilita el tratamiento oportuno para el paciente.

The Biotime S100-β Rapid Quantitative Test is intended to quantify the concentration of S100-β 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 neurological injury.