Labnovation Technologies, Inc. |
|
Rapid Antigen Test Kit CoV-2 Antigen Saliva Rapid Test Kit Simple
Operation 1 Test Professional Testing Rapid Test Kit
Intend Use
The rapid test kit is qualitative detection if SARS-CoV-2 antigen
in human saliva samples and people who have been suspected person
with symptoms within 9 days from onset. The test result can be used
for early triage and rapid management of suspected population, but
not used as the sole basis foe 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 |
Name | SARS-CoV-2 Antigen Saliva Rapid Test Kit |
Model Number | LX-401601 |
Type | 1 Test / Kit |
Warranty | 24 Months |
Certification | CE, MSDS |
Quality | ISO1345, ISO9001 |
Storage Temperature | 2℃-30℃ |
Specimen Type | Saliva |
Sample volume | 3 Full drops |
Specification | 78*34*125 MM |
Package | Single Pack |
Product Feature
Principle
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. | Etc. |
Certificate