STANDARD F COVID-19 Ag FIA is the fl uorescent immunoassay for the qualitative detection of specific nucleoprotein antigens to SARS-CoV-2 present in human nasopharynx. STANDARD F COVID-19 Ag FIA should be used with the STANDARD F Analyzers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection.

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.

STANDARD F COVID-19 IgM/IgG Combo FIA is the fl uorescent immunoassay for the qualitative detection of specific antibodies to SARS-CoV-2 present in human serum and whole blood. STANDARD F COVID-19 IgM/IgG Combo FIA should be used with the STANDARD F Analysers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to diagnosis of SARS-CoV-2 infection in convalescent phase of patient with clinical symptoms with SARS-CoV-2 infection.

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

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.

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.

STANDARD M SPIN-X Viral RNA Extraction Kit provides high yield and purity viral RNA extraction from clinical specimens.

STANDARD™ M SARS-CoV-2 qualitatively detects SARS-CoV-2 virus infection from upper and lower repiratory sample of suspected patient. Reverse transcription real-time polymerase chain reaction (Real-time RT-PCR) is used to amplification and detection of SARS-CoV-2.