Coronavirus Test Kits Covid 19 Test Kits Suppliers and Manufacturers

.SOFTEC COVID-19 Antigen Test Kit (For Celt Test Use) Fast Easy to Use Reliable The SARS-CoV-2 Antigen Rapid Test (Nasal Swab) is a single-use test kit designed to detect SARS-CoV-2, the cause of COVID-19, with a self-collected nasal swab sample. The test is intended for use in symptomatic individuals who meet the definition of COVID-19 disease and is limited to asymptomatic individuals who have been in contact with confirmed or suspected cases of COVID-19 and at-risk healthcare workers. The SARS-CoV-2 Antigen Rapid Test (Nasal Swab) is a qualitative membrane-based immunoassay for the detection of SARS-CoV-2 nucleocapsid protein antigens in a human swab sample. There are single packs and 25 pieces of products. SOFTEC COVID-19 Antigen Test Kit (For Self-Test Use) (Pack of 25) The price of the product is determined by the number of orders.

Specimen Collection: Nasal, Saliva Packing: 1 test / 25 Tests Accurancy: >93% Specificy: 99% Warranty: 2 year Certificate: CE, ISO13485,BfArM,BASG,MDA,Thai FDA

A box 2 doses I HEALTH price $6+10% A Box 1 dose Flow Flex Price $4.4 +10% You can be seller mandate DDP USA AND ALL OVER WORLD ATTENTION PAYMENT SBLC or BCL /PB Moq 500K MAX 5-10MX12Month DDP USA or World BY AIR Buyer side 50% Commission open You can be seller part 10% of 50% for you SOP: 1, Documents NCNDA ICPO KYC 2 Seller FCO 3 DRAFT SPA DRFT SBLC OR BCL /PB 4 SPA sign &IMFPA 5 ATTENTION PAYMENT SBLC/BCL /PB / TT 6,Can get Allocation letter after confirm payment 7 DDP buyer Port Inspection pay TT 8 Then keep rolling for next deal Notice 1,You can Mark up 2 you can be seller part 3 DDP to your warehouse 2022 Feb 26-Mar 10

GENEDIA W COVID-19 Ag (Nasal swab) 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

Application Suspected case test in epidemic area Early test of fever clinic and CDC Screening of primary medical institutions Inspection of floating population in public areas 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. Parameters: A Short Test Time: 15 mintues B Accuracy: More than 98.1% C Sensitivity: 96.4% Specificity: 100% D Easy operation: Nasal Swab E One Step solution F Lower cost with high efficiency G Package: 1 Test/Kit, 5 Tests/Kit, 25 Tests/Kit H It can detection for Omicron Virus

Rapid antigen test kit for detection of COVID-19 . Easy,safe and accurate

European CE Certified 15 Minutes Detection Time Format 25T/Kit Colloidal Gold Method Detection Substance: Antibody Type of Sample : Serum/Plasma/Whole Blood No instruments needed

1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit 2. Brand Name: NIL 3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection 4. Class of Medical Device: Class D 5. Shelf life :15 months 6. Sterile/Non-Sterile: Non-Sterilized 7. Contains Drugs: No 8. Medical Device Grouping Category: IVD-Kit 9. Grouping Description: Intended for qualitative determination of COVID-19 infection 10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s). 11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen. SALIENT FEATURES: â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate â?¢ HRP Conjugated Polyvalent Anti-Human IgG â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins) â?¢ Strip Format Microwell Plate â?¢ Ready to use Substrate and Controls â?¢ Only 20 pL of human serum is required for measurement in duplicate. â?¢ Works on any open ELISA system â?¢ Assay procedure is easy to automate OUR TEST: â?¢ Principle: Indirect ELISA â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows: â?¢ Diagnostic sensitivity is 100% (>98%) â?¢ Diagnostic specificity is 98.67% (>97%) â?¢ PPV: 94.12�°/0 â?¢ NPV: 100% Please contact us for more information and product details.

a) WHO certified kit b) CE Certified Kit THE ABOVE GIVEN PRICE IS EX-FACTORY VAPI WARE HOUSE

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.

We Supply Grade A medical examination Covid-19 Test Kit with affordable prices in major international market free to contact us for more Quotation.

We Supply Grade A medical examination Covid-19 Test Kit with affordable prices in major international market free to contact us for more Quotation.

NAME COVID-19 Nucleic Acid Detection Kit(PCR-fluorescent Probe) USE Diagnosis COVID-19 rapidly for public disease control Manual Biological cabinet, Appropriate real time PCR instrument, Appropriate nucleic acid extraction system or kit, Desktop centrifuge ( suitable for 96- well plate or 8-strip tube), Centrifuge with a rotor for 0.2ml reation tubes or plate. Vortex mixer, Adjustable piperres(with maximum capacity of 2 L, 10L, 50L, 100L, and 200L, respectively), Disposible pipette tips with filters, Disposable powder-free gloves, RNase FREE 1.5mL centrifuge tube, PCR reation tube / PCR reaction plate. Storage and Transportation Store in -20 - 5 and transport with carbon diaxide ice, avoid being repeated freezing and thawing. Expiration date 9 months * Please be noted the above is the price including the tax, NOT FOB.

supply convid-19 test kits, top product, with TV certificate-. stock available immediately in Germany, and could deliver all over the world

hrough market research and government trading department internal documents, we have complied a covid-19 related products suppliers contract info. The data consists of product introduction (including description and certification) and main markets they export. Supplier�¢??s name and contact person phone number. All the contract person are the one who directly responsible for international selling, and the phone number is her/his direct mobile phone. 100% accurate and updated at the end of March 2020 The data consists of 6 categories 1. Diagnostic reagent supplier (eg. Covid-19 test kit etc.) 2. Medical equipment (like ventilators etc.) supplier 3. Chinese patent medicine supplier 4. AI-aid diagnostic system supplier 5. Temperature measuring device supplier (eg. Thermometer etc.) 6. Disinfection equipment (eg irradiation system and disinfection gel, hand wash etc.) 7. Protective clothing Each categories price: USD 100 Full package of seven categories: USD: 600

The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals. This test has been authorized by the FDA under a EUA for professional use CLIA and CLIA WAIVED for Point Of Care. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. This product is intended for professional use and not for home use. FACT SHEET FOR HEALTHCARE PROVIDERS This test has been authorized by the FDA under a EUA for use by authorized CLIA laboratories. This device is CLIA waived for point of care use for fingerstick whole blood specimens only. The user should be trained in the procedure. Wear appropriate protective attire for your safety when handling patient samples. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. There should be a blue line in the control region (next to ) before testing, discard the device if there is no blue line.