Rapid Test Covid 19 Suppliers and Manufacturers

Rapid Test (COVID-19 IgG-IgM) with quality certificate and fast delivery. Minimum order: 20000 pcs / 800 cartons Packing: 25 pcs test + a leaflet + a bottle of buffer in the box, 80 boxes (size: 64x38.5x47cm) Delivery time: immediately after payment confirmation Payment terms: 50% against the invoked performance and 50% after confirmation of the product. Mode: FOB I greatly appreciate the opportunity to serve you. For more information on this and other products and orders in general, please contact us. Phone/Whatsapp: +55 71 9 8249-2742 E-mail: enenterprise@outlook.c(o)m Best regards, Euclides Neto.

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

380 000 pcs single package SELF-TEST 1pcs KIT Goldsite CE1434 LAIENTEST NASAL Price start from 1.79 IFU inside EN / DE / PL BOX PL / EN / DE Optional PDF IFU FR / IT / ES / DA Our warehouse in Poland! We are authorized distributor

Covi-G (powered by Cipla) Rapid Test kit combines quality, efficacy and convenience - offering precise results in 10-15 mins Features & Benefits Covid IgM-IgG Serologic Rapid Test for COVID-19 is used to qualitatively detect IgG and IgM antibodies against SARS-CoV-2 in whole blood in vitro Precise and effective - Tests for both IgM and IgG antibodies - Sensitivity and specificity comparable to highest available offerings Sensitivity: IgG 92%, IgM 82%; Specificity IgG 97%, IgM 94% - ->92% total accuracy: IgG 96,5% - IgM: 92,8% - High reproducibility (consistent results across the same patient) - High quality, reliable & convenient - Single-prick blood test - 10-15 minutes per test - Intuitive visual interpretation - No specialized training or equipment needed - Portable hence highly scalable - Storage at room temperature (2-30 C) - Conformance to CE (Europe) and ISO manufacturing The Covi-G platform for Rapid Antibody tests has a set of unique and unparalleled offerings SUSTAINABLE QUALITY Validated Declaration of CE conformity - Launched in Feb 2020, among the earliest technologies/ kits to declare CE-compliance, and continuing strong compared to competitors - Under process for receiving USDA E authorization Among only 3 integrated vendors of Rapid tests Developed and manufactured in Europe (Belgium) - One of the very lew players manufacturing in Europe, with zero complaints also certified locations ACCEPTABILITY ACROSS MARKETS Demonstrated capabilities in local countries validation - Independent local studies conducted in Belgium and France, validating the sensitivity and specificity of the product Participated in published research - Covl-G kit compared lavorably with 7 lgFL IgM rapid antibody tests and IgG ELISA in a comparative study published by Elsevier Science Direct, verifying sensitivity of the kit PROVEN COMMERCIAL EXPERIENCE Sold in 25+ countries already - Including Europe, US, Canada, Africa and multiple developed and emerging markets - Under participation in govt tenders Robust manufacturing capability and capacity - ISO-certified manufacturing site - Ability to cater to high manufacturing volumes from Belgium, to ensure adequale QA and commercial viability AFFORDABLE AND SCALABLE Viable to scale up at Institutions and Retail level - Economical cost per-unit established over many months of process improvement and local manufacturing - Can cater to insured as well as out-of pocket populations Continuous improvement through R&D - Multiple rounds of performance testing complete, further testing in 5 reputed hospitals underway in Belgium, France, USA and Canada - Other platforms including Rapid antigen testing also being developed The price is per unit, the minimum is 25000 units

Coronavirus Ag Rapid Test Cassette (Swab) have been placed on the European Market, based on the following performance characteristics (which are also included in the IFU included in each test kit) Coronavirus Ag Rapid Test Cassette (Swab) Method Coronavirus Ag Rapid Test Cassette Total Results Relative Sensitivity: 86.7% Relative Specificity: 100% Accuracy: 96.3% Coronavirus Ag Rapid Test Cassette (Swab) The CE mark has been applied as the products fit the definition of an in vitro diagnostic medical device as defined in the IVD Directive and are classified as a general IVD products as they are not included in List A or List B, and they are not intended to be used by lay users. Please note that this

Specification Product Name VivaDiag SARS-CoV-2 IgM/IgG Rapid Test (COVID-19 IgM/IgG Rapid Test) Test Principle Colloidal gold Sample Type Whole blood (fingertip/venous ), serum or plasma Sample Volume 10 �¼L Test Time 15 min Operation Temperature 15-30 Storage Temperature 2-30 Shelf Life (Unopened) 24 months

Dear, We have Covid-19 rapid test kits which have all the certificates. We accept payment by LC. This product is a hot sale at the moment. The price is rising every single day. If you are interested, contact us. MOQ: 0.5 million - CIF: $9 Best Regards, Tuana Oztuna

It can be used for rapid screening of carriers of the virus that are symptomatic or asymptomatic. Recent studies suggest that a high percentage of patients show no clinical symptoms of the virus, thus screening patients is vitally important. The test is ideally suited for hospitals, clinics and test laboratories.

Antigen Rapid COVID 19 Test Simple nasal swab or nasopharyngeal swab under 30 minutes Sensitivity 97.10% TCID50 75.5 CE marked for diagnostic use in EU and associated countries Paul Ehrlich Institute and IVD Min order 10000 pcs Free delivery within Germany

10,000 Rapid Antigen Test 500 Boxes 20 Test Per Box CE CERTIFICATION

Format: Cassette Storage: 4-30�ºC Certificates: ISO13485 Specimen: Whole Bood,Serum / Plasma Read time: 10-15 Minutes Weight: 101g Sample rule Option 1: Offering existing samples Option 2: Customized samples based on customers' specifications Sample lead time 3-10days (depends on the style) Result: 15 Minutes Shipping mode 1.Sea shipment 2.Air shipment 3.Door to door parcel Intend to use 1.The New Coronavirus (Sars-CoV-2)Test is a rapid chromatographic immunoassay for the qualitative detection of Antibody(IgG) to coronavirus in human whole blood, serum or plasma specimens. 2.Common signs of coronavirus infection include respiratory symptoms, fever, cough, wheezing and dyspnea. In more severe cases, the infection can lead to pneumonia, severe acute respiratory syndrome, kidney failure and even death. Corona viruses can be excreted through respiratory secretions, transmitted through oral fluids, sneezing, contact, and through the air droplets spread. Positive:1. Two or three distinct lines appear. One line should always appear in the control line region (C), and another one or two apparent colored line(s) should appear in the test line region(s) (T1 and T2). 2. If a line appears on the quality control line, a line appears on the test line T1, and no sline appears on the test line T2, it indicates that IgG antibody is present in the sample and no IgM antibody is present. 3. If a line appears on the quality control line, a line appears on the test line T2, and no sline appears on the test line T1, it indicates that IgM antibody is present in the sample and no IgG antibody is present. Negative: One colored line appears in the control region (C). No Apparent colored lines appear in the test lines regions (T1 and T2). Invalid: Control line(C) fails to appear. Insufficient specimen volume or incorrect procedural technologies are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor. Note: The red line in the test line (T) can show different shades of color. However, even a very weak line should be judged as a positive result during the specified observation period, regardless of the color of the line.

Covid19 Rapid Test Kit Detection of virus in 5-10 minutes CE Certified 25 Kits in 1 Box MoQ is 10,000 pcs

GraceTree COVID-19 IgM/IgG Rapid differential detection kit for IgM and IgG against COVID-19 in human serum, plasma and whole blood 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 - Packing: 1 box of 25 Test units - Product Origin : South Korea - Certificate : FDA EUA Certificate will be proved near 15. September. 2020 - Shipping Terms : FOB - Payment Terms : T/T - MOQ : Under Discussion - Contract : Direct contract seller / Depending on volume, direct contract with a subsidiary of seller which is listed on stock market(in S.Korea) - LOI, POF needed for seller

Covid-19 Rapid Test Kits see website elkeisys.kr

There are, The product has the CE and FDA Declaration of Conformity. N 1 Box is made up of 25 tests for professional use which cannot be sold separately. Prices excluding Transport excluded Advance payment or to be settled on quantities charged with LC or Escrow LC and Escrow is accepted only for larger quantities you have 5000 boxes Delivery depends on the quantities available at the moment Departure from Magazzino Italia to Europe or to be agreed, For other states, possibility of departure from China