HCV Teste quantitativo rápido

HBSAG ..é o antígeno da superfície do vírus da hepatite B (HBV). Indica a infecção atual da hepatite B Biotime HBSAG ..Kit de teste quantitativo rápido pode detectar o espécime de soro e plasma.

The Biotime Dengue NS1 Antigen Rapid Test is intended to qualitatively detect the dengue NS1 antigen in human serum, plasma, or whole blood samples on the Biotime FIA Analyzer by fluorescent immunoassay. The test is used asthe earlyaid diagnosis and screening of dengue virus infection. For in vitro diagnostic use only. For professional use only.

The Biotime DengueIgG/IgM Antibody Rapid Testis intended to qualitatively detect the dengue IgG/IgM antibody in human serum, plasma or whole blood samples on Biotime FIA Analyzer byfluorescent immunoassay. The test is used asthe early aid diagnosis and screening of dengue virus infection.  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.

NT-probnp é um marcador para detectar a função cardíaca, com uma longa meia-vida e alta especificidade. Biotime NT-probnp Kit de teste detecta a quantidade de nt-probnp em sangue total humano, soro e plasma amostras.

The Biotime DengueIgG/IgM Antibody Rapid Testis intended to qualitatively detect the dengue IgG/IgM antibody in human serum, plasma or whole blood samples on Biotime FIA Analyzer byfluorescent immunoassay. The test is used asthe early aid diagnosis and screening of dengue virus infection.  For in vitro diagnostic use only. For professional use only.

O autoteste combinado COVID-19 ag & flu A/B é uma imunocromatografia de ouro coloidal destinada à detecção qualitativa e diferenciação rápida in vitro , simultânea da proteína N de sars-cov-2, influenza A e influenza B diretamente de amostras de swab nasais obtidas de indivíduos, suspeitos de infecção por COVID-19, influenza A ou influenza B. os resultados são para a identificação simultânea da proteína N de sars-cov-2, influenza A e influenza B.

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.