OEM ODM Convenient 1 Test ART Self Test Kit Saliva Specimen

Rapid Test Kit SARS-CoV-2 Antigen Saliva Rapid Test Kit 1 Test For Self Testing Protable Rapid Antigen Test Kit

Intend Use
This rapid test kit is intended for the qualitative detection of SARS-CoV-2 antigen in human saliva sample from novel coronavirus suspected person with symptoms within 9 days from onset. The test result can be used for early detection and triage of people suspected of being infected. 

Product Details

Product  Feature

• Protable and convenient
• High Accuracy, Sensitivity and Specificity
• Excellent Performance, Clean background
• Easy for use, One step oerate process

 
Main Components

• 1 Test Cassette
• 1 Saliva Collectors With Collection Tube
• 1 Sample Extraction Buffer
• 1 Package Insert

 
Use Step

Note: Bubbles are likely to occur during sample processing and blowing. Do not add bubbles when dropping samples to the sample well of the test cassette.

• Open the cap of the collection tube and istall saliva collector.
• Put the collection tube with saliva collector close to lips and let the saliva flow into the collection tube. Tje volum of saliva needs to be half of 0.5 scal mark(0.25).
• Screw the sample extraction buffer carefully.

• Add all sample extration buffer to the collection tube. Discard the saliva collector, tighten the cap onto the specimen collection tube.
• Shake the specimen collection tube at least three time vigorously to mix the saliva and the extraction buffer. Squeeze bottom of the collection tube ensure the saliva is thoroughly mixed.
• Add 3 full drops of the solution to the sample well(S). Read the result at 15 minutes. Do not interpret the result after 20 minutes.

 
Result Interpretation

• POSITIVE: Two (2) distinct colored lines appear. One line should be in the control region (C) and the other line should be in the test region (T).

• NEGATIVE: One (1) colored line appears in the control region(C). No apparent colored line appears in the test region (T). The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than the minimum detection limit.

• INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.

 

 
Virus Sources

Limitation

• The test results of this kit are only for the reference of clinicians and should not be taken as the sole basis for clinical diagnosis and treatment. Clinical management of patients should be considered in the light of their symptoms/signs, medical history, other laboratory tests and treatment responses.
• Restricted by antigen detection reagent method, the lowest detection limit (sensitivity analysis) is generally lower than that of nucleic acid detection, so the researchers deal with negative result to give more attention, should be combined with other test results comprehensive judgment, advice to doubt the negative result of nucleic acid detection or virus isolation culture identification method for review.
• False negative results may be caused by unreasonable sample collection, transport and treatment, and low viral load in samples.

FAQ

• Production quantity?

It depends on the specification of the products. For big orders, we can produce 100k-250k per day.

• Have after-sale service?

Yes we support technical services. And if the goods are missing due to our fault, we promise to compensate.

• Register your products in our country?

Yes. We can offer full files for you to register.

• Lead time?

Stock 3-7 days in general. Or please contact us by email for specific lead time base on your order quantities.

• Support ODM or OEM?

Yes we support both. If needed,welcome to discuss details with us.