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.
A serology test or Antibody Rapid Test which doesn't test for the virus itself. Instead, it look for body's immune response to the virus. This test is getting popular is not only because its convenience but also because it can identify whether youâ??ve ever been exposed to SARS-CoV-2 - which would deepen our understanding of who is getting sick, particularly people who showed few or no symptoms. It could also allow people whose bodies seem to have some degree of immunity to the illness to return to work more quickly. Please email us and get detailed factsheet, certification etc.
GOLD STANDARD for diagnosis novel coronavirus. This kit is based on one-step RT-PCR technique. Used for the in vitro qualitative detection of novel coronavirus (2019-nCoV) ORF1ab and N gene in the throat swabs, sputum specimens of suspected pneumonia patients infected by novel coronavirus, suspected clustering cases and others needing diagnosis or differential diagnosis for novel coronavirus. No cross-reaction, sensitivity is 500 copies/ml. CFDA/CE. Applicable Instruments include ABI 7500 & LightCycler480.
Availability: 6M units as per today 21.11.21, goods ready to go, with an option to extend Price: $4.20 per unit Comms open: $0.10 Delivery: 10-14 days from deposit 30% (CIF USA, Air freight) Payment terms: 30% deposit upon order confirmation, 70% upon receipt of Documentation â?? Documents are: Packing list, SGS, AWB, Letter of Export and Invoice Note: Must be as per FDA cleared under EUA, buyer responsible for custom clearance (7%). Seller can give a guarantee, PB. Procedure: PO to our partner, who is direct to the allocation holder.
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.
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.
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
Anti-SARS-CoV-2 Rapid Test, COVID-19 1. Easier: No special equipment needed, Intuitive visual interpretation. 2. Rapid: Quick sampling by fingertip blood, Results in 10-15min. 3. Accurate: Results with IgG and IgM respectively. 4. Application: as screening tool for potential suspect patients in large numbers. Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate Antibody Performance Measure Estimate of Performance 95% Confidence Interval IgM Sensitivity (PPA) 95.7% (289/302) (92.8%; 97.5%) IgM Specificity (NPA) 99.7% (311/312) (98.2%; 99.9%) IgG Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) IgG Specificity (NPA) 99.4% (310/312) (97.7%; 99.8%) Combined Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) Combined Specificity (NPA) 99% (309/312) (97.2%; 99.7%) Combined PPV at prevalence = 5% 84.4% (64.6%; 94.6%) Combined NPV at prevalence = 5% 99.9% (99.8%; 100%) Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate
Test Strip 50 for Blood Glucose Meter Accu-chek Active
Accu-Chek Performa 100 Test Strips (1 Box x 100 Each) Blood Glucose Test Strips
We are suppliers of BEST QUALITY One Touch Test Strip and looking for serious buyers in need of our products, contact with us for more details OneTouch Ultra Blue Diabetic Test Strips provide fast and less painful testing of glucose levels. Designed for use with the OneTouch Ultra Soft Automatic Blood Sampler and OneTouch UltraSoft Lancets, this blood test strip is ideal for diabetic patients who need to monitor their body glucose level at home.
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
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
COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of
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)
Fast results Easy visually interpretation Simple operation, no equipment required High accuracy The HAV IgG/IgM Rapid Test is for the qualitative detection of IgG and IgM antibodies to Hepatitis A virus (HAV) in whole blood, serum or plasma specimen as an aid in Hepatitis A diagnosis.
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.
