SD Biosensor

  • STANDARD F CK-MB FIA is a fluorescent immunoassay for the quantitative measurement of Creatine Kinase Isoenzyme-MB level in human serum and whole blood. This test is to screen and monitor the Acute Myocardial Infarction (AMI).
    Specimen Serum, Whole blood
    Sample volume 100µl
    Range 1~200ng/mL
    Time 15mins
    Temperature 2-30? / 36-86?
    Shelf life 18 months
    Requires Standard F Analyzer system 
     
  • STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained
    Specimen Plasma, Whole blood
    Sample volume 10µl
    Measurement Range 25-5,000mg/mL
    Time 7mins
    Temperature 2-30? / 36-86?
    Shelf life 18 months
    Requires Standard F Analyzer system 
  • STANDARD F hs-CRP FIA performs quantitative measurement of high-sensitivity C-Reactive Protein (hs-CRP) in serum, plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.
    Specimen Serum, Plasma, Whole blood
    Sample volume 5µl
    Range 0.1-15.0mg/L
    Time 3mins
    Temperature 2-30? / 36-86?
    Shelf life 18 months
    Requires Standard F Analyzer system 
  • STANDARD F NT-proBNP FIA is a quantitative test for the determination of the N-terminal pro brain-type natriuretic peptide (NT-proBNP) level in human serum and whole blood(EDTA).
    Specimen Whole blood (EDTA), Serum
    Sample volume 100µl
    Measurement Range 0 ~ 25,000pg/mL
    Time 15mins
    Temperature 2-30? / 36-86?
    Shelf life 18 months
    Requires Standard F Analyzer system 
  • KOREA MFDS Approved 

    STANDARD F COVID-19 Ag FIA is the fluorescent immunoassay to detect SARS-CoV-2 infection in human nasopharyngeal swab specimen, identifying existence of SARS-CoV-2 viral nucleoprotein antigens.

    • Fast results as soon as 15 mins
    • Higher sensitivity than rapid test
    • Easy to use
    • Fluorescent Immunoassay (Europium)
  • This kit is the fluorescent immunoassay to detect the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid. KOREA MFDS Approved 

    STANDARD F COVID-19 IgM/IgG Combo FIA is the fluorescent immunoassay to detect the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

    • Fast results as soon as 15 mins
    • Higher sensitivity than rapid test
    • Easy to use
    • Fluorescent Immunoassay (Europium)
  • STANDARD F COVID-19 Ag FIA is the fluorescent 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.
  • This small fluorescence immunoassay device can perform qualitative and quantitative analysis on infections, respiratory diseases and chronic diseases, and it is operable with battery
  • 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.
  • 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.
  • 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.
    A more comparative overview can been seen in this table below:
  • This kit is the fluorescent immunoassay to detect the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

    The STANDARD M Flu/SARS-CoV-2 Real-Time Detection Kit is a real-time reverse transcription PCR assay for the simultaneous detection of Flu A, Flu B and SARS-CoV-2 nucleic acids in human nasopharyngeal swab, oropharyngeal swab, and sputum specimens.

    • Single tube reaction for detection of SARS-CoV-2, Flu A and Flu B
    • One-step Real-Time RT-PCR
    • Provide all reagents required for RT-PCR
    • Multiple SARS-CoV-2 target genes: ORF1ab and E gene
    • Conserved Flu target region: Flu A (Matrix gene), Flu B (NS1 gene)
    • Internal control: RNA process control (from NA extraction)
  • FDA EUA Approved  KOREA MFDS Approved  STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples.
    • One tube reaction for identification and detection of 2019-nCoV
    • One-step Real-Time RT-PCR
    • Provide all reagents required for PCR
    • Designed according to “WHO interim guidance for laboratory testing for 2019 novel coronavirus (2019-nCoV) in humans”
    • nCoV primers/probes ORF1ab (RdRp) gene, E gene
    • Provide Internal controls
  • WHO EUL  KOREA MFDS Approved  TGA Approved 

    STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.

    • Fast results within 15~30 mins
    • Easy to use
    • Specimen : Nasopharyngeal swab
    • All necessary reagents provided & no equipment needed
  • This kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

    STANDARD Q COVID-19 IgM/IgG Combo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.

    • Rapid testing for SARS-CoV-2 antibodies within 10~15 minutes
    • Specimen : Whole blood (20ul), serum , plasma (10ul)
    • Suitable for Point of Care Testing. No need for extra equipment
  • This kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

    STANDARD Q COVID-19 IgM/IgG Duo Test Kit is a rapid immunochromatography test designed for the qualitative presumptive detection of specific IgM and IgG to SARS-CoV-2 in humoral fluid.

    • Rapid testing for SARS-CoV-2 antibodies within 10 minutes
    • Just 10ul of specimen : Whole blood, serum , plasma
    • Suitable for Point of Care Testing. No need for extra equipment

Title

Go to Top