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
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
COVID-19 antigen rapid test Simple Accurate Safe 1 PU * (25 pieces) specificity 99.0%, sensitivity 97.3%, overall accuracy 98.1% From 4 PUs : one FFP2 mask per test free of charge * PU = Packing unit; 1 PU = 25 pieces; Offer valid while supplies last. For bulk orders of 1000 or more, please contact us
Antigen-COVID-19 Virus Test Kit (Colloidal gold) 25pcs/kit High quality Fast delivery CE certified
Rapid Tests Kits OTG USA COVID-19 Rapid Urine Antibody Test (World's First and Only) COVID-19 IgG / IgM Rapid Antibody Detection Test COVID-19 Saliva Antigen Rapid POC Test COVID-19 Antigen Rapid POC Test (Nasal Swab Collection)
Covid-19 Rapid Test Kits Results in 15 Min - MOQ 100,000- $9.15 USD Each Test -FOB-Abbott Antigen BinaxNOW Covid-19 Self Test (Nasal) (No Blood-No Saliva)
GENEDIA W COVID-19 Ag (Saliva) GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva
COVID-19 Rapid Antigen Self-Test Kit Indiaâ??s first COVID-19 test kit for self-use. Get your test results within 15 min from the comfort of your home & Office. So, there might be a time when you think you have contracted COVID-19 but cannot book a slot for an RT-PCR test. You might be asked to wait a couple of days. In such a circumstance, you can avail of a home/office corona testing� kit� such as Mylab CoviSelf COVID-19 Rapid� Antigen Test for COVID.� It is Indiaâ??s first COVID-19 home test kit to have earned the approval of the ICMR. Anyone above the age of 18 can use it at home. However, adult supervision is suggested if the test kit is used by people below 18. Intelligently Designed Filled with a solution that inactivates the virus and is designed in a manner to control & contain biohazard.
The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is lateral flow assay designed for the qualitative detection of specific SARS-CoV-2 antigen in human anterior nasal swab specimen. It is intended to be used for the detection of SARS-CoV-2 virus infection. The results obtained should not be the sole determinant for clinical decision. The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is intended for use for home self-testing. Platform: Immunochromatographic Assay Format: Cassette Detection Specific: SARS-CoV-2 antigen Specimen: Nasal swab Sensitivity: * 97.17% Specificity: * 100% Assay Time: 15-20 minutes Shelf Life: 18 months * Vs FDA Emergency Use Authorized real-time RT-PCR Suitable for: Individuals who wish to know their status on COVID-19 infection (symptomatic and asymptomatic regardless of their vaccination status)Individuals who have had close contact with COVID-19 positive patientsIndividuals with suspected exposure to coronavirusIndividuals who show symptoms related to COVID-19 (fever, dry cough, tiredness, sore throat,headache etc)Employees to perform regular testing to avoid workplace transmission Other appropriate and necessary screenings (such as International Entrance, cross-state, pre-employment screening, pre-admission to higher learning institutions etc.
We can provide Covid-19 Rapid Antigen Test. Test with reliable results within minutes. Made in the USA. Lateral flow assay, No equipment required, Results within 10 minutes, minimally invasive specimen collection, nasal swab, POC (in patient care setting). Detects SARS-CoV2 nucleocapsid protein antigen with ultra high performance. Identifies acute infection with 88.4% sensitivity and 100% specificity. Complies with FDA. Principals or Buyer's Mandates only. No broker chains. FOB or CIF. Minimum order 500000 test please.
10,000 Rapid Antigen Test 500 Boxes 20 Test Per Box CE CERTIFICATION
Covid-19 - Antigen - Schnelltests
The Pathocatch Coviself Covid - 19 Rapid Antigen test (RAT) is an in vitro diagnostic test for the qualitative detection of covid - 19 antigen in nasal swab specimens directly from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.
Health Canada Authorised Rapid Test The COVID-19 antigen rapid test device is a lateral flow in-vitro immunoassay intended to be used for the qualitative detection of the SARS-CoV-2 viral nucleoprotein. This device will detect both viable and nonviable virus in both nasopharyngeal and oropharyngeal secretions. This test had been authorized for point of care use by Health Canada and is available for immediate dispatch MediGuard Systems of Canada is an Authorised distributor of the Assuretech Rapid Antigen test. Support documentation and details available on request
a) WHO certified kit b) CE Certified Kit THE ABOVE GIVEN PRICE IS EX-FACTORY VAPI WARE HOUSE
nasal or throat swab, 25 tests per box, it has CE certificate
Product Make: Korea, India, China
Covid Antigen Ag swab rapid test card, Sensitivity: 96.17%; Specificity: >99.9%; Accuracy: 98.79% Big quantity, low price is available.
- Nasal test - Single packed with all component - Quick result within 15-20 minutes - Specificity 99,54% - Sensitivity 92,71% - Accuracy 97,14% - CE Home Certificate (EC Certificate No. 1434-YVDD-446/2021) Directive 98/79/EC Concerning in vitro diagnostic medical devices
This test quickly detects the presence of the antigen in a respiratory sample to determine whether your symptoms are due to SARS-Cov-2 infection.
