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CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer

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China Hangzhou AllTest Biotech CO.,LTD certification
China Hangzhou AllTest Biotech CO.,LTD certification
I like the products and service provided by AllTest. They really take our interest into consideration.

—— Mr John Smith England

My oldest daughter actually has Lyme disease. She spent almost 1 year in a wheelchair because of Lyme. She is doing very well now. I used 2 of the samples. 1 to test my Lyme diagnosed daughter and 1 to test my daughter who does not have Lyme. Your tests worked well. My daughter with Lyme tested positive and the one who does not tested negative.

—— Ms Sheila

Whenever I have the requests,AllTest always give me the satisfied reply at the first time.

—— Mrs Julie Tschetter Belgium

As the old customer of AllTest since 2009, we should thank the great work have been done by AllTest to support us gain more market share and profit

—— Mr Robin Seifert Germany

CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer

CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer
CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer

Large Image :  CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer Get Best Price

Product Details:

Place of Origin: China
Brand Name: AllTest
Certification: CE
Model Number: FI-NCP-502

Payment & Shipping Terms:

Minimum Order Quantity: N/A
Packaging Details: 10T/20 T
Delivery Time: 10-15 days
Payment Terms: T/T
Detailed Product Description
Color: Blue Specimen: Nasopharyngeal Swab
Cut Off: See Insert Storage: 2-30°C
Certificate: CE,ISO13485 Format: Cassette
High Light:

COVID-19 Rapid Antigen Detection Test

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Flurescence Immunoassay Analyzer Antigen Test

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CE Rapid Antigen Detection Test

The COVID-19 Antigen Test is a test for measuring COVID-19 antigens in Nasopharyngeal Swab specimens with the use of Fluorescence Immunoassay Analyzer.

 

【SUMMARY】

The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

Coronaviruses are enveloped RNA viruses that are distributed broadly among humans, other mammals, and birds and that cause respiratory, enteric, hepatic, and neurologic diseases.1 Six coronavirus species are known to cause human disease.2 Four viruses — 229E, OC43, NL63, and HKU1 — are prevalent and typically cause common cold symptoms in immunocompetent individuals.2


【SPECIMEN COLLECTION】

1. Insert a sterile swab into the nostril of the patient, reaching the surface of the posterior nasopharynx.
2. Swab over the surface of the posterior nasopharynx.
3. Withdraw the sterile swab from the nasal cavity.

CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer 0

【SPECIMEN PREPARATION】
Only the extraction buffer and specimen collection tube provided in the kit is to be used for swab specimen preparation.
1. Unscrew the cap of the specimen collection tube.
2. Insert the swab specimen into the specimen collection tube. Press against the inner wall of the tube and stir the swab for approximately 10 seconds while pressing theswab head against the inner wall of the tube to release the antigens in the collection
tube.
3. Remove the swab while squeezing the sides of the tube to extract the liquid from the swab.
4. Tighten the cap onto the specimen collection tube.

CE COVID-19 rapid antigen detection test With Flurescence Immunoassay Analyzer 1

【DIRECTIONS FOR USE】
Refer to FIATESTTM Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be conducted in room temperature.
Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.
1. Turn on the Analyzer power. Then according to the need, select “standard test” or “Quick test” mode.
2. Take out the ID card and insert it into the Analyzer ID Card Slot.
3. Add 3 drops of the solution (approx.120ul) to the sample well and then start the timer.
4. After 15 minutes of adding sample, Insert the test cassette into the Analyzer, click “QUICK TEST”, fill the test information and click "NEW TEST" immediately. The Analyzer will automatically give the test result after a few seconds.

 

 

INTERPRETATION OF RESULTS

Results read by the Fluorescence Immunoassay Analyzer and display the result on the screen.

Cat.No. Product Specimen Format Kit Size CE Status
FI-NCP-502 COVID-19 Antigen Test Nasopharyngeal Swab Cassette 10T/20 T CE

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Contact Person: selina

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