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Model No.: AT-002
Brand: Metest
Place Of Origin: China
Kind Of Power: Manual
Warranty Service: 2 Years, None
After-sales Service: None
Shelf Life: 2 Years
Product Quality Certification: Ce, Fcc, Rohs, Tuv
Medical Device Classification: Class Ii
Safety Standard: En 149 -2001+A1-2009
Packaging: box
Productivity: 10000000
Transportation: Ocean,Air,Express
Place of Origin: China
Supply Ability: 1000000000
Port: Ningbo,Yiwu
Payment Type: T/T,L/C,D/P,D/A,Paypal,Money Gram,Western Union,Others
Incoterm: FOB
Ningbo Autrends International Trade Co., Ltd. focuses on POCT reagents and The R & D, production and sales of the instrument have the independent research and development of antigen and antibody Development and production of biological raw material technology platform, as well as mature immune layer The analysis and dry biochemical diagnosis technology platform has developed and formed the valve cover poison Product testing, infectious disease testing, chronic disease testing, pregnancy testing Tumor detection, myocardial detection, biochemical detection, allergen detection, etc POCT reagents in eight fields.In the future, the company will still adhere to the principle of "providing excellent products for human health" The mission of "quality and service" and the vision of "becoming an evergreen tree in the industry", take "customer first, sustainable operation" as the enterprise value, and People oriented, honest and dedicated, down-to- earth, looking up at the stars and unity Progress, cooperation and innovation meet the needs of more scenario applications.
COVID-19/InfluenzaA+B/RSV/Adenovirus /M.pneumoniae Antigen Combo Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2, Influenza A+B, M.pneumoniae, Respiratory Syncytial Virus(RSV) and Adenovirus antigens present in human nasopharynx. ALL these tests can testing with LF Reader.
【HOW TO TEST】
Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.Remove the test cassette
from the foil pouch and use it within one hour.Best results will be obtained if the test isperformed immediately after opening the foil pouch.
Place the cassette on a clean and level surface. For Serum or Plasma specimen:
To use a dropper. Hold the dropper vertically, draw the specimen to the fill line (approximately 10mL), and transfer thespecimen
to the specimen well (S), then add 2 drops of buffer (approximately 80 mL), and start the timer.
To use a pipette: To transfer 10 mL of specimen to the specimen well(S), then add 2 drops of buffer (approximately 80mL), and start the timer
For Venipuncture Whole Blood specimen:
To use a dropper. Hold the dropper vertically, draw the specimen about 1 cm above the fill line and transfer 1 full drop(approx.10uL) of specimen
to the sample wel(S).Then add 2 drops of buffer (approximately 80 mL) and start the timer.To use a pipette: To transfer 10 mL of whole blood
to the specimen well(S), then add 2 drops of buffer (approximately 80mL), and start the timer
For Fingerstick Whole Blood specimen:
To use a dropper. Hold the dropper vertically, draw the specimen about 1 cm above the fil line and transfer 1 full drop(approx.10uL) of specimen
to the sample wel(S). Then add 2 drops of buffer (approximately 80 mL) and start the timer.To use a capillary tube: Fil the capilary tube and transfer
approximately 10mL of fingerstick whole blood specimen to thespecimen well (S) of test cassette, then add 2 drops of buffer (approximately 80 mL)
and start the timer. See illustrationbelow.
Wait for the colored line(s) to appear.Read results at 15 minutes. Do not interpret the result after 20 minutes.
Product Categories : Different Scenes COVID-19 IgG / IgM Detection Kit > Home Testing Kits
Privacy statement: Your privacy is very important to Us. Our company promises not to disclose your personal information to any external company with out your explicit permission.
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Privacy statement: Your privacy is very important to Us. Our company promises not to disclose your personal information to any external company with out your explicit permission.