Our COVID-19 rapid test kit can be used effectively on many levels for proper screening and strategic preparedness toward the pandemic. The test kit requires no sophisticated equipment nor laboratory settings. Our SARS-COV-2 Antibody Rapid Test Kit can be applied for screening of COVID-19 disease on the following: General practitioners and external clinics level to detect previous SARS-COV-2 viral infections on both symptomatic and asymptomatic patients. Determination of the immunity level of front-line healthcare workers, which can help in the development of pandemic preparedness strategies at national levels. Epidemiological COVID-19 surveys at national and district levels for research purposes. Airport screening for arriving /departing passengers to control the pandemic in the aviation industry. Suspected cases exclusion to minimize cost and time spent in the RT-PCR testing procedures. Screening on the national level to facilitate decision making regarding lockdown and curfew easing strategies. Phoenix Bioscience is offering a competitive price for a high-quality kit that is made in Canada and used currently to combat the pandemic in most American cities.
We at Phoenix Bioscience would like to offer you our COVID-19 rapid detection kit based on detecting SARS-COV-2 IgG and IgM and delivers results within 15 minutes. Made in Canada, CE certified. Packaging Details: Each package contains 25 individually packed tests, the buffer used in the detection procedure, and disposable pipettes for blood samples collection Phoenix Bioscience is offering a competitive price for a high-quality kit
Delivery: 2 days EXW China; 2 weeks EXW Europe Packing: 25pcs/box, 80box/ctn, ctn size is 64.5*38*47cm, N.W/G.W. is 17kgs/18kgs. MOQ: 20 cartons Reservation is required ! Payment 50% / 50 % before pick up EU certificates + declaration of conformity
Designed for qualitative detection of SARS-CoV-2 antibodies in human serum, plasma, and whole blood samples, novel coronavirus antibody detection reagent (Colloidal Gold Method) is regarded as auxiliary detection metrics towards on-site screening for suspected cases that have the negative results after nucleic acid testing. This rapid test can aid in the diagnosis of coronavirus infection and significantly shorten the detection time, yielding the results in 15 minutes.
Here we are finding distributor for corona virus Ab IgG/IgM whole blood rapid test device kit and Antigen Ag rapid test card, very high quality, CE mark is available! Covid Ab IgG/IgM Ab Whole blood test device Sensitivity: 99.6% Specificity: 99.31% Accuracy: 99.5% Covid Antigen Ag swab rapid test card Sensitivity: 96.17% Specificity: >99.9% Accuracy: 98.79% 10 miuntes to get the result. MOQ for each: 500 tests, 25 tests/box,
As Trilecem Company, we have rapid test kit for Covid-19 . We have all certificates.If you have any questions, you can contact me
2.8million Covid-19 Rapid Test Kits In Stock
Singclean Covid - 19 lgG lgM Rapid Test Kit - Colloidal Method
Intended Use Package Storage Specimen Type Shelf life Time to result Detection of SARS-CoV2 antigen 20 Tests / kit 1 - 40 Nasopharynx / Nasopharyngeal 24 months from manufacture date 5 - 8 minutes
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
1. Item : GraceTree COVID-19 IgM/IgG Rapid differential detection kit for IgM and IgG against COVID-19 in human serum, plasma and whole blood 2. Feature & Type : IgM/IgG 1) COVID-19 IgM/IgG : blood test 2) Dual-band results for simple interpretation 3) Multivariable analysis of immunoglobin IgG & IgM 4) Positive percent agreement (PPA) = 96.0% Negative percent agreement (NPA) = 98.99% 5) Room temperature storage ( 2~30C / 36~86F ) 6) Time to result : 2 min 7) Expiration date of this kit is 6 months after its manufacture date 8) MATERIALS PROVIDED - Test device individually foil-pouched with a desiccant - Assay solution in dropping bottle - Capillary tube for sample loading - Instructions for Use 3. Price : $350 = 1 box of 25 Test units (1 unit = $14) 4. Product Origin : South Korea 5. Certificate : FDA EUA Certificate will be proved near 15. September. 2020 6. Shipping Terms : FOB Payment Terms : T/T 7. MOQ : Under Discussion 8. Contract : Direct contract seller 9. LOI, POF needed for seller *NOTE : Volume is Unlimited
Result in 10 to 15 minutes, no equipment is required 25 pcs per box 50 boxes per carton about 600 cartons per FCL Shelf life 24 months
COVID-19 Rapid 99% Accuracy Mouth Testing Kits: Serology Antibody Testing $49.97 (FDA APPROVED) It is a 10-minute test that does not require a machine. â?¢ Antigen Rapid Testing $59.97 (FDA Emergency Use Authorization - EUA) It is a 20-minute test that does not require a machine or cold chain logistics� (as compared to PCR swab tests). Volume Discounts 10,000 plus units $5 per kit discount 20,000 plus units $7 per kit discount 50,000 plus units $10 per kit discount *Special Discount Structure for (immediate) higher volume orders* Please email for more information.
Softec Pregnancy Rapid Test kits
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
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 : 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)
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.
