Cat No : 11NCo10. SD biosensor STANDARD M nCoV Real-Time Detection kit is used for identification and detectionof novel coronavirus (2019-nCoV) ORF1ab (RdRp) gene and E gene in humannasopharyngeal swab, oropharyngeal swab, and sputum specimens using reversetranscription (RT) real-time PCR. This kit is helpful for the auxiliary diagnosis of 2019novel coronavirus disease (COVID-19). The test results are for clinical referenceonly and cannot be used as a basis for confirming or excluding cases alone.
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Product Description Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity Differentiates Between Igg And Igm To Determine Stage Of Infection One Step Procedure Minimizes Operator Error Due To Sample Preparation High Level Of Reproducibility Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
Genbody Influenza/ Covid - 19 Ag Triple, Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy. Production information: 1.Specimen: nasopharyngeal swab or Viral transport medium (VTM) 2.No Cross-reaction with 27 kinds of other respiratory viruses. 3.No interference with 23 kinds of interfering substances. 4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2. 5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax. Product specifications : Sensitivity - 100% Specificity -100% Rapid Result time within 20 - 30 Minutes. Detects P. falciparum and P. vivax. Storage at 1 40C. Specimen Type- Whole Blood
CTK biotech, OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood. CE certified.
CTK Biotech's , The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
WHO Approved, First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen. Sensitivity - 100% Specificity - 100% Rapid Result time within 20 - 30 Minutes. Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum Storage at 1 40C. Specimen Type- Whole Blood
CTK Biotech's, OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
CTK BioTech's ' Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL, Higher accuracy, sensitivity and specificity than the Guaiac Test, No dietary restrictions, Clear, easy-to-interpret result, Individually sealed foil pouches containing: One cassette test device,, One desiccant, Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011), Patient ID stickers, One package insert (instruction for use).
UNIQUE FEATURES: EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 �µL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 µL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers 70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patient's visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 µL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use).
Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen. Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2 10 µl of specimen: Serum, Plasma & Whole Blood Long term storage of 24 months at 2 - 30 C Complementary to RT-PCR Test Can be performed without extra equipment
Cat No: 41FK10. Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection.
Cat No : COVAG025. GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
Cat. No : 5513C. COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
Cat. No : F-NCOV-01G. 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.
Cat. No : ICO-3000. iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
The iFinDx COVID-19 IgM/IgG is a rapid test kit for differential detection of specific IgM and IgG against COVID-19 in human serum, plasma and whole blood.