Boson Selftest With Ce0123 Single Packge
PCL - Rapid Antigen Covid-19 test with saliva
15 min Rapid Covid - 19 Antigen Test
Real - Time OneStep RT-PCR based assay system for detection of 2019-nCoV (CE-IVD)
Rapid PCR(1 Hour) Seasun AQ-TOP COVID-19 Test
Covid-19 Total Antibody / Neutralizing Antibody Rapid Test Kit
SGTi-flex Rapid Antibody Test
GDL Swabs(Nasopharyngeal, Oral), Wooden Tongue Press
2019-nCoV Antigen Rapid Test Kit (Colloidal gold Assay) Specimen Type: Siliva Time to result: 15 minutes quick test Storage: 18 months (room temperature) Package: 25 Tests/Box ( 25 test cassettes + 25 Antigen extraction tubes + 25 Saliva sampling cups+ 25 Sampling droppers + 1 bottle Antigen extract R1 buffer+ 1 Test tube stand + 1 manual) Relative Sensitivity: 90.3%. New products will be launced in next 2 weeks, please mantain your attention! 2019-nCoV Antigen Rapid Test Kit (Colloidal gold Assay) Specimen Type: Nasopharyngeal Swab Time to result: 15 minutes quick test Storage: 18 months (room temperature) Package: 25 Tests/Box (25 pcs Nasopharyngeal swab + 25 test cassettes + 1 bottle Antigen extraction tube + 1 bottle Antigen extract R1) Relative Sensitivity: >85% Short test time: Within 15 Minutes Accuracy: More than 90% Easy operation: Throat/Nose swab, Saliva sample. One-step solution - Lower cost with high efficiency Components: A 25 test cassettes B 25 Antigen extraction tubes C 1 bottle antigen extract R1 D 1 Test tube stand E 25pcs Saliva Sample cups F 25pcs disposable droppers G 1 manual Application: A Suspected case test in epidemic area B Early test of fever clinic and CDC C Screening of primary medical institutions D Inspection of floating population in public areas Product Information: Product Name : 2019-nCoV Antigen Rapid Test Kit Methodology : Colloidal Gold Assay Size: 25 Tests/box Storage and Validity: Stored at 2-30 within 18 months Specimen: Nasopharyngeal Saliva Read the results in 15 minutes. A strong positive results may show within 15 minute. But the negative result must be reported after 15 minutes. And the results after 20 minutes are not valid anymore.
Self-test received notified body approved CE Marking on April 1, 2021 A home test for the rapid qualitative detection of SARS-Cov-2 virus antigen in anterior nasal swabs from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 Performance Characterisitics Sample tyep: nasal swab Time to result: 15-20 minutes Sensitivity: 97.70% Specificity: 99.84% Accuracy:98.97% Layperson study statistics 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly. Specifications 1 Test/kit Catalog No.: 1N40C5-2 Kit components: 1 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 1 sterilized swab 1 extraction tube 1 sample extraction buffer IFU Tube holder on back of box 5 Tests/Kit Catalog No.: 1N40C5-4 Kit components: 5 Rapid SARS-Cov-2 Antigen Test Card (sealed foil pouch) 5 Sterilized swabs 5 extraction tubes 5 sample extraction buffer IFU 1 tube stand 20 Tests/Kit Catalog No.: 1N40C5-6 Kit components: 20 Rapid SARS-Cov-2 Antigen Test Card (sealed foil pouch) 20 Sterilized swabs 20 extraction tubes 20 sample extraction buffer IFU 1 tube stand
The lab indicated that the recombinant protein of Indian mutant (B.1.617.2), A.23.1(Unit Kingdom), AT.1 (Russia), B.1.1.7(Unit Kingdom), B.1.351 (South Africa), B.1.616 (France), B.1.621 (Colombia), C.36 (Egypt), C.37 (Peru), P.1 (Japan/Brazil), P.2 (Brazil) can be detected by Jinwofu SARS-CoV-2 Antigen Test Kit. For the newly descovered mutant Omicron(B.1.1.529), we performed sequence alignment analysis on its mutation sites, and found that all the mutation sites were outside the epitope region recognized by the monoclonal antibody selected by our company. By bioinformatics analysis, Jinwofu SARS-CoV-2 Antigen Test Kit can also effectively detect mutant Omicron(B.1.1529)
Ihealth Antigen Rapid Test, MOQ 100k tests, DDP USA CA warehouse from factory directly. DM for details.
We are a manufacturer of SARS-CoV2 (Covie-19) antigen RAPID TEST CASSETTE. The Genesea SARS-CoV-2 Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection the antigen from SARS-CoV-2 in nasal swab, nasopharyngeal swab, oropharyngeal swab specimens. The products have CE certification, We can provide you at cheapst price. Delivery time 5days. Capacity 10million tests/month
100 Percent USA Made FDA EAU and CE approved rapid Antigen and Antibody test kits.
DEAR, LIVE STOCK BELGIUM MOQ : 500 PRICE : 2,5â?¬/ TEST + delivery cost 1 pack First come, First served
Covid antigen rapid test kit made in Turkey seller : manufactory company minimum order : 10,000 pcs Licensed in Europe and UK 1 box 25 pcs T/T
This is Product is very demand due to pandamic situation. We are supplying ICMR approved ,CE certified product
We are supplier of ICMR approved ,CE certified test kits for Dengue and Malaria with international standard
3.000.000 of COVID-19 rapid tests available on stock in Romania; 1 to 2 days for delivery everywhere in Europe. We are the European representative of the Korean manufacturer of covid-19 rapid detection kit 1. GENEDIA W COVID-19 Ag, nasopharyngeal differential detection of COVID-19; 2. GENEDIA W ONE COVID-19 IgM/IgG differential detection of COVID-19 IgM and IgG; 3. GENEDIA W COVID-19 Ag (SALIVA) All the tests have CE mark, exceptional sensitivity and quality, can be used both by medical staff and for self-testing. All documentation is available upon request,
[Intended Usage] This kit is used for the in vitro qualitative detection of suspected cases of pneumonia caused by New Coronavirus infection, patients with suspected clusters, other patients who need to be diagnosed or differentially diagnosed with the New Coronavirus infection, and nasopharyngeal swabs, oropharyngeal swabs, and bronchoalveolar lavage fluid samples of patients with mutation beads for the New Coronavirus ORF1ab and N gene, S gene N501Y mutation and S gene E484K mutation sites. [Storage Conditions & Validity] 1. The kit should be stored frozen at -20 and protected from light; the expiration date is 6 months; the production date and expiration date are shown in the outer packaging box. 2. Avoid repeated freezing and thawing of the kit and the number of freezing and thawing shall not exceed 7 times. 3. After opening, the bottles should be stored at -20 and protected from light. The number of bottles opening times should not exceed 7 times, which will not affect the use within the validity period. [Applicable Instruments] 1. This kit has been validated on ABI7500 quantitative fluorescence PCR instrument. 2. For other models not listed, relevant experiments have not been performed or completed for this kit. If users need to use this type of instrument platform to carry out the detection of this reagent, please contact our Technical Department at for relevant support. NB: The other devices can include quantitative fluorescence PCR platforms with FAM, VIC, ROX and Cy5 channels. [Sample Requirements] 1. Nasopharyngeal swabs, oropharyngeal swabs and other methods are used to obtain samples, and it is recommended to use commercial virus sampling kits for sample collection devices. [Test Results Interpretation] 1. Negative and positive controls should be tested in each experiment and the test result can be determined only when the controls meet the quality control requirements. 2. When FAM, VIC and ROX channels are positive, Cy5 channel result may be negative due to the system competition. 3. When the internal standard result is negative, if the FAM, VIC and ROX signals of the test sample are also negative, the test result of the sample is invalid, and the cause should be found and eliminated, and the experiment repeated for this sample. [Product Performance Index] 1. Precision: The coefficient of variation Intra-batch / Inter-batch, Intra-day / Inter-day among different operators shall not be higher than 5.0%. 2. Coincidence rate of negative positive controls: The coincidence rate of positive controls and negative controls is 100%. 3. Minimum detection limit: The minimum detection limit of this kit is 500 copies/mL. [CE Mark Registration No.]: RPS/499/2021. [EC REP.]: CMC MEDICAL DEVICES & DRUGS S.L. C/ Horacio Lengo n18, C.P 29006, Milaga, Spain.
