Product Details:
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Total Accuracy: | 98.02% | Specimen: | Saliva |
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Quanlity Guarantee Period: | 18 Months | Group: | Universal |
Storage Temperature: | 2℃-30℃ | Package: | 1 Test / Kit |
Specification: | 78*34*125MM | Application: | Daily Checks |
High Light: | Single Pack Home saliva test kits,ISO 9001 home saliva test kits,98.02% self rapid test kit |
Antigen Saliva Test SARS-CoV-2 Antigen Saliva Rapid Test Kit Single Pack Self-test For Home Use
Intended Use
This rapid test kit is intended for the qualitative detection of SARS-CoV-2 antigen in human saliva samples from novel coronavirus suspected person with symptoms within 9 days from onset. Positive result of the antigen test can be used for early triage and rapid management of suspected populations, but it cannot be used as diagnosis basis of SARS-CoV-2 infection. Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions. Further nucleic acid detection should be carried out for suspected population whose antigen test result is positive or negative.
Product Details
Item | Value |
Model Number | LX-401602 |
Package | 1 Test / Kit, Single Pack |
Warranty | 18 Months |
Safty Standard | ISO13485 |
Sample Type | Saliva |
Sample volume | 3 Full drops |
Test Speed | Within 15 minutes |
Use | For Self-test At Home |
Specificity | 99.00% |
Sensitivity | 94.29% |
Product Feature
Test Principle
Main Components
Use Step
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
Global high frequency mutation | Alpha / B.1.1.7(U.K.) | Beta I B.1.351(South Africa) |
Gemma I P.1(Brazil) | Kappa I B.1.617.1(India) | Delta I B.1.617.2(India) |
C.37,ect | Alpha I B.1.17(U.K.) | B.1.36.16.etc |
A.2.5,etc | A.23.1 | Alpha I B.1.17(U.K.) |
B.1.1.33.etc | C.1.1.etc. |
Advantage
Contact Person: Ld
Tel: +8613480985156