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Standard Q H.Pylori Ag

Standard Q H.Pylori Ag STANDARD Q H.pylori Ag Test is an immunochromatographic assay for the detection of Helicobacter pylori antigen in the human stool sample. Users can easily and rapidly get the accurate result of the test within 10 minutes. Intented Use STANDARD Q H.pylori Ag Test is an immunochromatographic assay for the detection of Helicobacter pylori antigen in human stool sample. Easy to use, Easy to read and interpret Room temperature storage

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STANDARD Q H. pylori Ab

STANDARD Q H. pylori Ab STANDARD Q H. pylori Ab performs qualitative analysis by detecting antibodies specific to Helicobacter pylori in serum, plasma and whole blood using immunochromatography. With a simple test method, With its high sensitivity and specificity, the screening test result can be obtained within 10 minutes. Intented Use STANDARD Q H. pylori Ab Test is a rapid chromatographic immunoassay for the qualitative detection of specific antibodies to H. pylori present in human serum, plasma or whole blood. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of H. pylori infection in patients with clinical symptoms with H. pylori infection. Advantage Getting a fast result in 10-20 minutes. Easy handling, which does not require specific training. Suitable for Point Of Care Testing. No follow-ups or equipment required. Room temperature storage Specification Specimen Whole blood, Serum, Plasma Test time 10-20 minutes Specimen volume 10µl (Serum, Plasma) / 20µl (Whole blood) Storage temperature 2-40℃ / 36-104℉

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Standard Q HCV Ab

Standard Q HCV Ab STANDARD Q HCV Ab qualitatively analyzes antibodies specific to hepatitis C virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis C infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes. Easy to use, Easy to read and interpret Room temperature storage Intended Use STANDARD Q HCV Ab Test is a rapid chromatographic immunoassay for the qualitative detection of specific antibodies to HCV present in human serum, plasma or whole blood. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of HCV infection in patients with clinical symptoms of HCV infection. It provides only an initial screening test result. More specific alternative diagnosis methods should be performed in order to obtain the confirmation of HCV infection. STANDARD Q HCV Ab Test is intended to be used by trained healthcare or laboratory professionals or other health care workers who have received appropriate training. This product can be used by trained lay providers operating in point-of-care settings in resource-limited lower- and middle-income countries. This product is not intended for self-testing.

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Standard Q Malaria P.f Ag

Malaria P.f Ag STANDARD Q H.pylori Ag Test is an immunochromatographic assay for the detection of Helicobacter pylori antigen in the human stool sample. Users can easily and rapidly get the accurate result of the test within 10 minutes. Intended Use STANDARD Q H. pylori Ag Test is a rapid chromatographic immunoassay for the qualitative detection of H. pylori antigen present in faecal specimens. This test is for in vitro professional diagnostic use and is intended as an aid to early diagnosis of H. pylori infection in patients with clinical symptoms of H. pylori infection. It provides only an initial screening test result. Advantage Getting a fast result in 10-15 minutes Easy handling, which does not require specific training Suitable for Point Of Care Testing No follow-ups or equipment required Room temperature storage Specification Specimen Faeces Test time 10-15 mins Specimen volume 40-70 mg Storage temperature 2-30℃ / 36-86℉  

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Standard F Tnl FIA

Standard F Tnl FIA STANDARD F TnI FIA performs quantitative measurement of Troponin I (TnI) level in plasma and whole blood specimens using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained. Intended Use STANDARD F TnI FIA is a fluorescence immunoassay for the quantitative determination of cardiac Troponin I (cTnI) levels in human serum and whole blood using STANDARD F Analyzers, manufactured by SD BIOSENSOR. This test is an in vitro diagnostic use and intended for use as an aid in the screening and monitoring of acute myocardiac infarction (MI). Advantage TnI is a cardiac marker for the diagnosis of myocardial infarction Automatic strip recognition by reading the information stored in 2D barcode Reagents can be stored at room temperature Plasma and Whole blood specimens available

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