Product Details
Antigen Rapid Test Kit CE Certification SARS-CoV-2 Antigen Rapid
Test Kit Single Packing Self Testing Rapid Test Kit
Intend Use
- In Vitro Diagnostic Reagents rapid test kit
- Qualitative detection
- Self diagnostic antigen rapid test use
- Qualitative detection of the nucleocapsid protein antigen from
SARS-CoV-2
Diagnostic Accuracy
Product Feature
Simple operation step without extra instrument
Short testing time, get the result within 15 mionutes
Lower cost with high effciency
Safety and reliable, import of raw materials with high quality
Main Components
- 1 Test Cassette
- 1 Sample tube with prefilled sample extraction buffer
- 1 Swab
- 1 Instruction for use
Use Step
- Open the SARS-CoV-2 Antigen Rapid Test Kit, lay all the supplied
materials on a clean, dry and flat surface.(Please check the
expiration date printed on the BOX. Do not use it beyond the
expiration date.)
- Please check the expiration date printed on the BOX. Do not use it
beyond the expiration date
- Take a sample tube (with prefilled sample extraction
solution).Remove the aluminum foil sealing of the prefilled sample
extraction tube and then put the tube into the tube stand.
- Gently, insert the entire absorbent tip of the swab (around 1.5 cm)
into your nostril. Slowly, rotate the swab in a circular against
the inside walls of your nostril 5 times or more. Be sure to
collect any nasal drainage that maybe present on the swab. Gently
remove the swab. Use the same swab to repeat steps in the other
nostril and slowly, take out the swab.
- Dip the swab into the sample extraction liquid after sample
collection, fully immerse the tip of the swab, rotate and squeeze
the swab 10 times, then pull out the swab, and take the stranded
liquid as much as possible.
- Close the cap of the sample tube. Add 3 full drops of the mixed
solution vertically into the sample well (S) of the test cassette.
Read the result 15-20 minutes after adding the sample. Result got
after 20 minutes is invalid.
Result Interpretation
POSITIVE: Two colored bands appear on the membrane. One band appears in the
control region (C) and another band appears in the test region (T).
NEGATIVE: Only one colored band appears, in the control region (C). No apparent colored band appears in the test region (T).
INVALID: If there is no Control line (C) or only a Test line (T) in the result window, the test did not run correctly and the
results are not valid.
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. | others |
Applicable
Certificate
Company Profile
Labnovation Technologies, Inc. is an original manufacturer
established in Shenzhen, China since 2001. We are dedicated in
developing and manufacturing IVD instruments and reagents including
HbA1c analyzer and reagents, rapid test reader & reagents,
hematology reagents, clinical chemistry reagents, electrolyte
reagents, wash solution and urine test reagents.
Labnovation products are developed in house, tested extensively in
clinics and passed strict quality controls. All of our products are
CE marked and approved by SFDA. In the past 15 years, our products
have been exported to 110 different countries and used in 8000
hospitals worldwide. We provide both ready-to-use final products
and bulk OEM reagents, including ready-to-use reagents,
concentrated, and powder.
With an investment of 10% of our annual sales into R&D, we
release new products every years. We win more and more domestic and international cooperation by
company reputation and products quality while we actively take part
in fairs like MEDICA,AACC, ARBA HEALTH and so on through which we
are well-known by the companies in this field.