USD$18.00 AccuPowe COVID-19 Real-Time RT-PCR Kit is an in vitro diagnostic kit that helps diagnose COVID-19 infections, detects SARS-CoV-2 (E gene and RdRp gene) RNA from a suspected infection patient's sample (such as sputum, nasopharyngeal swab, oropharyngeal swab) through Real-Time Polymerase chain reaction(PCR) using ExiStation Universal MDx system. Validated to: Bio-Rad CFX96 ABI 7500 Fast Target Genes: Rdrp, E
For the qualitative assessment of COVID-19(SARS-CoV-2) neutralizing antibody after the vaccination in human serum/plasma/whole blood. Sensitivity: 95.39% Specificity: >99.9% Accuracy: 98.47% CE Certificate available.
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is an immunofluorescent sandwich assay. It can detect the virus with very high sensitivity and specificity. When the sample is applied to the sample wells, SARS-CoV N protein and labeled antibody complexes are formed and travel up the strip. The labeled microsphere fluorescent probe reagent is used to form a visible red line with a matched UV flashlight. The presence of SARS-CoV-2 will be indicated by a visible red test line (T) in the result window. The membrane is pre-coated with Chicken IgY on the control (C) line. Control (C) line appears in each result window when the sample has flowed through the strip.
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus. View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus. View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
Product Details: Brand Abbott ICMR Approved Yes Test Method Antigen Test Result Time (Rapid Kits) 15 min Packaging Size 25 Test Kits/Box Cat. No 41FK10 Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection
RAPID TEST IgG/IgM - EMERGENCY RESPONSE KIT FROM THE UNITED STATES! The COVID-19 Rapid Test for Screening, Diagnosis, and Monitoring is a lateral flow immunoassay, a way to qualitatively assess the presence of IgG and IgM antibodies specific for SARS-CoV-2 from a person sample Product advantages COUNTRY OF ORIGIN The United States EARLY DISCOVERY Individual test avoids cross-infection WHOLE SPECTRUM The cover early, mid and late phase of the disease FAST RESULTS 10 minutes HIGH ACCURACY 98,43% EFFICIENCY Two types of tests on one cassette with quick result SAFETY Individual test avoids cross-infection
STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples. - One tube reaction for identification and detection of 2019-nCoV - One-step Real-Time RT-PCR - Provide all reagents required for PCR - Designed according to WHO interim guidance for laboratory testing for 2019 novel coronavirus (2019-nCoV) in humans" - nCoV primers/probes ORF1ab (RdRp) gene, E gene Provide Internal controls Kindly check ghope-ppe.com. All information is for a consumer. If you want to buy a bulk, please contact us.
The GENEDIA W COVID-19 Ag is an in vitro diagnostic single-use test and qualitative immunoassay to detect SARS-CoV-2 antigen in nasopharyngeal swab and sputum specimen from human. This assay is designed for professional personnel in laboratory and at point-of-care as an aid in screening patients suspected of being infected and asymptomatic patients. Allow wider testing with fast test time (10 minutes) Clinically proven data of asymptomatic patients available Separately packed extraction solution to minimize the possibility of contamination No additional instruments required Package Unit : 20 Tests/Kit Expiration Date : 24 Months (while sealed in the original aluminum foil pouch) 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 The price is negotiable according to the amount of your order and shipping term. No MOQ is required but we prefer 1 pallet with 9,600 tests. (20 tests/kit, 30 kits/carton, 16 cartons/pallet)
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
DYMIND COVID-19 Antigen Test Kit (Saliva Test Kit) - For Self Testing SARS-CoV-2 Antigen Test Kit (colloidal gold method) MALAYSIA DRUG AUTHORITY (MDA), KKM APPROVED Accurate + Fast + Easy Sensitivity: (95% CI): 123/129 95.35% (90.15% -98.27%) Specificity: (95% CI): 160/16398.16% (93.84% -99.33%) Ct count
BinaxNOW COVID-19 Antigen Self Test (2 tests for serial testing) A simple solution for COVID-19 infection detection, with rapid results. This test has received FDA Emergency Use Authorization for self-testing without the need to ship samples to a lab or for a prescription from your healthcare provider. This 15-minute test can be completed anytime, anywhere. Simply test yourself twice within 3 days, with at least 36 hours between tests. MOQ 50,000 Worldwide Shipping
Covid 19 Rapid Antigen Test Kits Brand: Healgen Scientific Antigen Protein Swab Rapid Test 96% Accurate 15 Minute Response
Cat No: 41FK10. Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection.
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The n-FasT SARS-CoV-2 diagnostic kit, has the Lamp method, which is among the most reliable detection methods. The reaction that reveals the diagnosis result for Covid-19 in a fast, practical and safe way yields results with a colorimetric method based on colour change. n-FasT differs from all other kits with the opportunity to give results below the patient within 30 minutes in application and with 97 % success rate result interpretation.
COVID-19 Test Kits
Manufacturer: Shanghai LiangRun Biomedicine Technology Co.,Ltd. Certificates: CE(EU), MHRA(UK), HSA(Singapore), MDA(Malaysia), TSE(Turkey), DIGEMID(Peru), Luxus Medical(Germany) , FDA(US), EUA(US, Registering) FOB: 10m, 4.5usd
COVID-19 TESTING KIT title Sample Collection And Preparation. Keep The Kit And Sample To Room Temperature Prior To Testing. Add Sample ( 20 Ul Pf Serum/Plasma/Whole Blood ) To The Sample Well By Using A Micropipette/Dropper. Add Buffer ( 1 Drop For Serum/Plasma Or 3 Drop For Whole Blood ) To The Sample Well Immediately. Wait For The Colored Lines(S) To Appear And Read The Result At 10 Minutes. The Result Is Valid Within 20 Minutes.
* MOQ 100K tests or Below : $6.0/test * 100K ~ 1M : $5.9/test * Over 1M : $5.5/test * FDA APPROVED! Price is keep increasing due to extreme demand from the USA. * PROCEED ASAP!
