Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test. Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling. (A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test (B) Price $4 EXW (c) Origin: Canada (d) Features: Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection. (E) HS code:382200 (F) 20,000 units (g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg. 25,000 kits per pallet.
Product Description FDA EUA, CE Price of product ( USD price or FOB price) : "10,000-99,999: $8.45 100,000-249,999:$7.98 250,000-499,999: $7.78 500,000+: Contact" Product origin : China Minimum Order Size and Packgaing details : 10,000 Individual tests (25/box)
Usage/Application Hospital Type Rapid Test Kit Results 3 mins Packaging Size 100 Tests Country of Origin Made in India The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only. SALIENT FEATURES Rapid visual test ,based on Flow Through Technology. Differential detection of HIV-1 & HIV-2. Detection of group O & subtype C Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2. 100% sensitivity & 100% specificity as per WHO Evaluation. Shelf life 15 months at 2-8�°C Available in convenient pack sizes-10 Tests, 50 Tests and 100 Tests. Results within 3 minutes. No instrument required. In built quality control dot.
Antibody 01 Quickly obtain test results in 15 minutes. 02 High detection efficiency: simultaneous monitoring of IgG and IgM. 03 Detection without any testing equipment. 04 Sample type: Whole Blood/Serum/Plasma. Antigen 01 Quickly obtain test results in 15 minutes. 02 Detection without any testing equipment. 03 Sample type: Nasal specimen or oral specimen.
Test kits for covid-19 We have testing kits for Covid-19 In inventory now for immediate shipping. High sensitivity rapid test kits for Covid-19. 250K available now for USA and international shipping, Inventory moving fast.
2019 nCOV Detection Kit (2019-nCoV) IgG/IgM� Rapid Test kit Approved by FDA LineGene K Plus Real-Time PCR Detection System Model FQD-48A
COVID-19 (Sars-CoV-2) antibody test kit now available. -Diagnosis for coronavirus disease (COVID-19) -Easy to use, instant result in 15 minutes Product name : SARS-CoV-2 Antibody Test (Lateral Flow Method) Packing size : 20 tests per box Reaction Time] : 15 mins Sample type : Whole blood, serum and plasma Storage condition : 2~ 30 Shelf life : 12 months Qualification : CFDA, CE
Nasopharyngeal Swab Test painless Medical Sampling Test Rapid Detection Test kit
The self testing product is transformed from the professional testing product CLUNGENE COVID 19 Antigen Rapid Test manufactured by Clongene The BfArM has granted the first special approvals according to 11 paragraph 1 of the German Medical Devices Act ( of antigen tests for self administration by laypersons (self tests) for the detection of SARS CoV 2 Our self testing product can be sold and used in Germany Overview of CLUNGENE COVID 1
INTENDED USE The Helicobacter-Pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of H. pylori infection. INTRODUCTION Helicobacter pylori (also known as Campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma. The epidemiologic study shows that more than 50% of the world's population is infected by H. pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by H. pylori strains. So the detection and treatment of H. pylori strains infection is very important. At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical ELISA and immunoblot assays. This Kit belongs to non-invasive approach.
INTENDED USE The One Step Dengue NS1 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in serum or plasma to aid in the diagnosis of Dengue viral infection. SUMMARY Dengue is transmitted by the bite of an Aedes mosquito infected with any one of the four dengue viruses. It occurs in tropical and sub-tropical areas of the world. Symptoms appear 3��14 days after the infective bite. Dengue fever is a febrile illness that affects infants, young children and adults. Dengue haemorrhagic fever (fever, abdominal pain, vomiting, bleeding) is a potentially lethal complication, affecting mainly children. Early clinical diagnosis and careful clinical management by experienced physicians and nurses increase survival of patients. One step Dengue NS1 Ag Test is a simple, visual qualitative test that detects dengue virus NS1 antigen in human serum or plasma. The test is based on immunochromatography and can give a result within 15 minutes. 25PCS/BOX
USA Manufactured, highly accurate, rapid COVID-19 Antigen test. Clinically validated by third-party medical institutions in USA and Europe (Denmark, Poland). The test is highly specific and sensitive (Specificity 100%, Sensitivity 99.1%). Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.
USA Manufactured, highly accurate, rapid COVID-19 Antibody test. Clinically validated in the USA by Harvard and UCSF Universities, and found to be best-in-class of Antibody tests. 95-100% accuracy in identifying patients after days 12. Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.
Corona Antigen Rapid Test Kits USD 4.85 FOB.
Accu-Chek test strips are essential components of blood glucose monitoring for individuals with diabetes. These strips are designed to work seamlessly with Accu-Chek blood glucose meters, enabling accurate and reliable measurement of blood sugar levels. The strips utilize advanced technology to require only a small blood sample, making the testing process more comfortable. With rapid and precise results, Accu-Chek test strips empower users to effectively manage their diabetes by providing valuable insights into their current glucose levels. This user-friendly and indispensable tool plays a crucial role in facilitating proactive health management for individuals living with diabetes.
A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) Clear, dependable results in 15 minutes Requires minimal training and no equipment So easy it can be used at the lowest levels of health care service Can use whole blood or serum/plasma Collection can be by fingerstick or venipuncture No refrigeration required Storage conditions 2-30�°C
CAT No : RCHM-02071. The CareStar COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.
Product Details: Number of Reactions(Preps)/Kit :30T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 10 min CAT No : RK019-30 STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes. Easy to use, Easy to read and interpret Discrimination between HIV-1 and HIV-2 antibodies Room temperature storage Performance Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
Antigen Test Kit (Colloidal Gold) Certified : US_FDA, Thai FDA, TGA, TUV, CE Marked Nasopharyngeal Swab , Oropharyngeal Swab, Limit of detection, The limit of detection has been evaluated at 0.5 ng/mL. Please note. due to high demand of product. First come, First Get terms applied. Price FOB
CTnI One Step Troponin I Rapid Test Kit (Whole blood/serum/plasma) 1.Product description Introduction: Product name: CTnI One Step Troponin I Rapid Test Kit Specification: Lateral-flow Immunofluorescence Chromatographic Assay 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Type: Cassette MOQ: 10,000 PCS Analytical Range: 1.0~50ng/ml (Whole Blood); 0.1~50ng/ml (Serum/Plasma) Specimen: Human serum/plasma/whole blood Manufacturer: Hangzhou Laihe Biotech Co., Ltd. Clinical significance 1. Diagnosis of various chest pain 2. Foundation of ACS diagnosis and risk stratification 3. Best markers for ACS prognosis 4. An aid in the diagnosis of myocardial infarction (injury) 5. Can improve clinical, economic and operational outcomes Principle Insert the sample cassette into Immunofluorescence Quantitative Analyzer. The detection system will scan the markers and bond zone to gain optical signals, and then analyze the signals to get the concentration of the tested sample. Storage Valid for 24 months under 4-30 °C with aluminum foil bag packing. Once opened, the cassette is valid for 1 hour. 2.Application Clinical Laboratory, ED, ICU, CCU, Respiratory Department, Cardiology Department, Pediatrics Department, Surgery Department, Hematology Department, etc.
