Adenitan

STANDARD F200 Analyser

STANDARD F200 Analyser STANDARD F200 Analyzer is a fluorescence immunoassay device that can perform qualitative and quantitative analyses on infections, respiratory diseases and chronic diseases, and it supports convenient user interface and LIS/HIS connectivity. Optimized for field diagnostics with small size (Clinic, Laboratory) Recognize information stored in 2D barcode Internal quality control LIS/HIS connectivity Intended Use This fluorescence immunoassay device that can perform qualitative and quantitative analysis on infections, respiratory diseases and chronic diseases supports convenient user interface and LIS/HIS connectivity.

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STANDARD Transport Medium

STANDARD Transport Medium STANDARD Transport Medium is intended for the and transport of clinical specimens containing viruses, Chlamydiae, Mycoplasma or Ureaplasma from the collection site to the testing laboratory. Bacterial and fulgal flora inhibition Internal conical tube that can stand alone Available multiple tests with large volume of transport medium Stable at room temperature Intended Use Transport Medium is intended for the transportation and preservation of clinical specimens containing viruses, Chlamydiae, Mycoplasma or Ureaplasma.

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STANDARD Q COVID-19 Ag Saliva

STANDARD Q COVID-19 Ag Saliva STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in Saliva specimens with mucus. Test time : Within 15 mins Easy and convenient testing process for professionals Effective in detecting the SARS-CoV-2 variant Effective in detecting the SARS-CoV-2 variant No need for extra equipment Intended Use STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in human saliva specimens with mucus. This test is for administration by healthcare workers and labs only, as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection. It provides only an initial screening test result. This product is strictly for medical professional use only and not intended for personal use. The administration of the test and the interpretation of the results should be done by a trained health professional. The result of this test should not be the sole basis for the diagnosis; confirmatory testing is required.

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Standard Q Covid -19 Ag

STANDARD Q Covid -19 Ag STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in human nasopharynx. Test time : Within 15 mins Easy and convenient testing process for professionals Effective in detecting the SARS-CoV-2 variant Suitable for Point of Care Testing No need for extra equipment Intended Use STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in human nasopharynx. This test is for administration by healthcare workers and labs only, as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection. It provides only an initial screening test result. This product is strictly for medical professional use only and not intended for personal use. The administration of the test and the interpretation of the results should be done by a trained health professional. The result of this test should not be the sole basis for the diagnosis; confirmatory testing is required.

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STANDARD F Sars-Cov-2 nAb FIA

STANDARD F SARS-Cov2 nAb FIA STANDARD F SARS-CoV-2 nAb FIA is the fluorescent immunoassay for qualitative measurement of circulating neutralizing antibodies against SARS-CoV-2 in human serum and plasma. High correlation with VNT (Virus neutralization test) POCT type of neutralizing antibody test Available for testing by variant group (Group 1: Wuhan/U.K, Group 2: Brazil/South Africa/Japan) Rapid test result (35mins) Intended Use STANDARD F SARS-CoV-2 nAb FIA is a fluorescent ammunoassay for qualitative measurement of neutralizing antibodies against SARS-CoV-2 in human serum. This test is intended for use as an aid in detecting neutralizing antibodies against SARS-CoV-2 virus for purposes of clinical surveillance, post-infection screening, and post-vaccination screening.

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