Intended Use The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen. Salient Features Based on “Flow Through Technology”, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity. Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device. Detection of all the subtypes of HCV. Results within 3 minutes. In built quality control dot which validates the test. 100% Sensitivity & 98.9% Specificity as per WHO evaluation. Shelf life : 24 months at 2-8°C

Intended Use Advantage Dengue NS1 Ag card is a rapid solid phase Immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen in Human serum /Plasma.This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue Infection. Salient Features Rapid test based on lateral flow technique. Detection of Dengue in the seronegative stage i.e. from Day 1 of fever. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). Results with in 20 minutes Longer shelf life : 30 months at 2-30°C. Convenient pack size : 25 tests Sensitivity-96% and Specificity- 98%

This product performs qualitative analysis on NS1 antigens of Dengue virus in serum, plasma and whole blood. Intented Use STANDARD Q Dengue NS1 Ag Test is an immunochromatographic assay for the detection of NS1 antigens in human serum, plasma, or whole blood samples. This test kit is for use in in-vitro diagnostic procedures. Specification Specimen Whole blood, serum, plasma Test time 15-20mins (Inaccurate results after 20 minutes) Sensitivity 92.9% (184/198) Specificity 98.7% (222/225) Storage temperature 2-40℃ / 36-104℉ Advantage Getting fast results In 15 ~ 20 minutes Wide storage range of 2~40℃ (36~104℉) Easy and convenient testing process Effective in detecting the antigen(NS1 protein) Suitable for Point of Care Testing No need for using extra equipment

The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite Troponin I Combo Rapid Test is intended to be used by healthcare professionals as an aid in the diagnosis of acute myocardial infarction (AMI). Any use or interpretation of this preliminary test result must also rely on patient’s symptoms and the professional judgment of a physician. A more precise test method such as an instrument method must be used to confirm the test result obtained by this device. Normally the level of cTnI in the blood is very low. cTnI is released into the blood stream in forms of free cTnI and cTnI-C-T complex at 4-6 hours after myocardial cell damage. The elevated level of cTnI could be as high as 50 ng/mL during 60-80 hours after AMI and remains detectable for up to 10-14 days post AMI. Therefore, circulating cTnI is a specific and sensitive marker for AMI. Clinical performance: Relative Sensitivity: 95.8% (95% CI: 91.5-97.9%) compared to a reference CLIA Relative Specificity: 99.7% (95% CI: 98.8-99.9%) Analytical sensitivity: The detection limit of cTnI is 1.0 ng/mL or greater in serum, plasma or whole blood specimen Cross-reactivity: No cross reactivity with 10 µg/mL skeletal muscle TnI, 2,000 ng/mL cardiac muscle TnT, 20 µg/mL cardiac muscle Myosin Dose hook effect: No hook effect was observed for cTnI at concentrations up to 3,521 µg/mL Interference: No interference was seen with 20 mg/dl Acetaminophen, 20 mg/dl Acetylsalicylic acid, 10.5 g/dl Albumin, 20 mg/dl Ascorbic acid, 1,000 mg/dl Bilirubin, 20 mg/dl Caffeine, 800 mg/dl Cholesterol, 200 mg/dl Creatinine, 20 mg/dl Gentistic acid, 1,000 mg/dl Hemoglobin, 600 mg/dl Oxilic acid, 1,600 mg/dl Triglycerides Shelf life: 24 months Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R3002, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Insert MedlinePlus: Troponin Test Poster

The 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. Uses serum, plasma or whole blood specimen Utilizes recombinant antigen derived from the CHIK structure protein IgM immunoassay is the most practical lab method Distinguish from dengue infection which presents with similar symptoms Clinical performance: Sensitivity: 90.4% Specificity: 98.0% comparing to a commercial ELISA Cross-Reactivity: no cross-reactivity found on 10-40 specimens from the 14 disease states and special conditions, such as dengue, Zika, malaria, HIV, TB, HAV, pregnant woman and others No interference with some common substances, such as Acetominophen (20 mg/dL), Heparin (3000 U/L), Ascorbic acid (20 mg/dL), Human IgG (1000 mg/dL), Bilirubin (20 mg/dL), Glucose (55 mmol/L), Creatinine (442 μmol/L), Salicylic acid (4.34 mmol/L), EDTA (3.4 μmol/L), Sodium citrate (3.8%) Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (5 μL) Sample diluent (REF SB-R0066, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Inserts U.S. CDC Chikungunya Virus Homepage: (Transmission, Prevention, etc.) WHO: Chikungunya Virus Fact Sheets

Malaria Pv/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of specific antigens of Plasmodium vivax (Pv) pLDH and Plasmodium falciparum (Pf ) HRP-2, in human whole blood. For professional use only. Relative Sensitivity for Pf HRP II: 98.5% Relative Sensitivity for pv LDH: 100% Relative Specificity for Pf HRP II: 99% Relative Specificity for pv LDH: 99% Pack Size: 50 Tests

Malaria Pan/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for simultaneous and differential detection of Pan (LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae) and Plasmodium falciparum HRP-Il, in human whole blood. For professional use only. Relative Sensitivity for pHRP II: 98.5% Relative Sensitivity for pan LDH: 100% Relative Specificity for pHRP II: 99% Relative Specificity for pan LDH: 99% Pack Size: 10 Tests

Malaria Pan/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Pan LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae and Plasmodium falciparum HRP-II, in human whole blood. For professional use only. Relative Sensitivity for pHRP II: 98.5% Relative Sensitivity for pan LDH: 100% Relative Specificity for pHRP II: 99% Relative Specificity for pan LDH: 99% Pack Size: 50 Tests

The Malaria Antigen test - Pf is an in-vitro diagnostic ready to use test based on the principle of lateral flow chromatographic immunoassay for qualitative detection of histidine rich protein (HRP-II) of Plasmodium falciparum (P.f.) in human whole blood. Relative Sensitivity: 99% Relative Specificity: 98% Pack Size: 50 Tests