Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.
Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea
Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.
Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.
for Rapid test
HCV Core+NS3+NS4+NS5 (IgG indirect)
HCV Core+NS3+NS4+NS5 (for coating, Sandwich)
HCV Core+NS3+NS4+NS5 (for conjugating, Sandwich)
Fapon Biotech provide gene engineering recombinant antigens of HCV, which can be used in ELISA, Rapid Test Kit and research, with high sensitive specific and stability.
Quicking canine coronavirus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine coronavirus (ccv ag) in dog's feces or vomit.
We are suppliers of 2 Covid-19 Rapid Test Kits, 1. Biozek Medical from Netherlands (MHRA UK & Saudi FDA) and Egens from China ( US FDA) approved kits. Please feel free to contact us regarding any material required regarding Covid-19
Rapid 2019-nCoV IgG/IgM Combo Test Card is an immunochromatography based one step in vitro test. It is designed for the rapid qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma, or whole blood. Rapid 2019-nCoV IgG/IgM Combo Test Card is a supplement detection for COVID-19 suspected infected patients besides nucleic acid test, which could greatly raise the accuracy of the detection for COVID-19.
25 tests/box, CE Mark and ISO, Clinical report, Certificate of analysis (COA)
Clinical specify >98.89%
Accuracy: 93.41%
Specimen: whole blood/serum, 10 minutes to get results
Canine parainfluenza virus(cpiv) is a highly contagious viral respiratory disease, which contributes to upper respiratory disease and infectious tracheobronchitis. Cpiv is often associated with other respiratory tract viruses. It will infect dogs of all ages that have not been vaccinated or previously infected, when young puppies will suffer more.
With the one step cpiv ag test kit, cpiv can be easily and acurately diagnosed within 10 minutes without any complex lab procedure
Principe: the kit is a solid phase chromatographic immunoassay using direct sandwich method.
Specimens: respiratory tract secretions or serum
Kit composition: 10 pouches, each containing one cpiv ag card with sucker and desiccant; 10 tubes with sample extraction buffer; 10 single packed swabs; one instruction for use
Quicking feline leukemia virus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of feline leukemia virus antigen (felv ag) in catí»s blood.
Assay time: 10-15 min
Sample: serum, plasma or whole blood
Shelf life: 18 months
Storage temperature: room temperature.
10 tests/kit
****kit component
-10íßfoil pouches, each containing one cassette, one pipette and a desiccant
-10íßassay buffer tubes (0.5 ml each)
-10íßcentrifugal tubes
-product manual
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
* 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
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
3. Price : $350 = 1 box of 25 Test units (1 unit = $14)
4. Product Origin : South Korea
5. Certificate : FDA EUA Certificate will be proved near 15. September. 2020
