Oscar Chikungunya test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Chikungunya specific antibody (IgM/IgG) in human serum/ plasma for diagnosis of Chikungunya infection. For professional use only. Pack Size: 10 Tests Several methods can be used for diagnosis of chikungunya virus infection. Serological tests, such as ELISAs may confirm the presence of IgM and IgG anti-chikungunya antibodies. The virus may also be directly detected in the blood during the first few days of infection by both serological and virological methods (particularly reverse transcriptase–polymerase chain reaction (RT–PCR)). There is no specific antiviral drug treatment for chikungunya. The clinical management targets primarily to relieving the symptoms, including the joint pain using anti-pyretics, optimal analgesics, drinking plenty of fluids and general rest. The joint pain is often very debilitating; it usually lasts for a few days, but may be prolonged for weeks, months or even years--the name “chikungunya” derives from a word in the Kimakonde language, meaning “to become contorted”, and describes the stooped appearance of sufferers with joint pain (arthralgia).

Intended Use Advantage Chikungunya IgM Card is a visual, rapid, sensitive, qualitative immunoassay for the detection of Chikungunya specific IgM antibodies in human serum or plasma. Salient Features Based on Sandwich Immunoassay principle. One step test procedure. Results within 15 minutes. Bio hazard free, fully covered, see through device. No Instruments required. Excellent Sensitivity & Specificity. Long Shelf life: 30 months at 2-30° C. Convenient pack size:10 Tests

STANDARD F Chikungunya IgM/IgG FIA qualitatively analyzes Chikungunya virus specific IgM and IgG antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity. Intented Use This product performs qualitative analysis on Chikungunya virus specific IgM and IgG antibodies in serum, plasma and whole blood. Advantage Able to perform qualitative analysis with high sensitivity and specificity by using fluorescent substance Objective result - Eliminates the subjectivity of a visual result Automatic strip recognition by reading the information stored in 2D barcode

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

Oscar Dengue Antibody Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane , for simultaneous and differential detection of dengue specific antibody (IgM/IgG) in human serum / plasma for diagnosis of dengue infection. For professional use only. Sensitivity: 97% Specificity: 98% Pack Size: 10 Tests

Oscar Dengue Ag (NS-1) and Ab (IgM/IgG) test device is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane , for simultaneous and differential detection of dengue specific antigen (NS-1) and antibody (IgM/IgG) in human serum / plasma for diagnosis of dengue infection. For professional use only. Sensitivity: Dengue antigen (NS1) : 98% Dengue antibody (IgM/IgG) : 97% Specificity: Dengue antigen (NS1) : 99% Dengue antibody (IgM/IgG) : 98% Pack Size: 10 Tests

Oscar Corona Antibody Detection Test is a rapid test based upon lateral flow immunochromatography principle for the qualitative detection of antibodies against Novel Corona Virus (COVID-19) in human serum, plasma or whole blood. For professional and in-vitro diagnostic use only. Sensitivity: 97.66% Specificity: 99% Pack Size: 25 Tests

INTENDED USE The Finecare™ PSA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative detemination of Prostate Specific Antigen (PSA) in human whole blood, serum or plasma. The test is used as an aid in diagnosis of prostatic cancer. STORAGE AND STABILITY 1. Store the test kit at 4~30℃ up to the expiration date 2. If removed from refrigerator, allow the test for 30 minutes to return to room temperature before testing. 3. Do not remove the device from the pouch until ready to use. The test cartridge should be used within 1 hour once opened.

Chikungunya Ab WHOLE BLOOD RAPID TEST For Qualitative Detection of Chikungunya Ab Whole Blood Rapid Test Type : Device Pack Size : 25 T