Rapid Nasal Oropharynx Swab COVID-19 Antigen Test Kit For Suspected Population

Brand Name:LABNOVATION
Certification:ISO13485,ISO9001,CE
Model Number:LX-401301
Minimum Order Quantity:10000 Pieces
Delivery Time:5-7 work day
Payment Terms:T/T, D/A, D/P
Contact Now

Add to Cart

Active Member
Location: Shenzhen China
Address: 101 and 5th Floor, Building 1, No. 68,18th Road, Guangming Hi-Tech Park, Tangjia Community, Fenghuang Street, Guangming District, Shenzhen 518107 ,China
Supplier`s last login times: within 29 hours
Product Details Company Profile
Product Details

Rapid Antigen Test Kit COVID-19 Antigen Rapid Test Kit High Quality Simple Operate Professional Use Rapid Antigen Test Kit


Intend Use

This rapid test kit is intended for the qualitative detection of SARS-CoV-2 infection from patients. It is for professional use only. It is an aid in the diagnosis of the patients with suspected SARS-CoV-2 infection in conjunction with clinical presentation and results of other laboratory tests. Results from this test kit should not be used as the sole basis for diagnosis.

Product Details

ItemValue
Product NameSARS-CoV-2 Antigen Rapid Test Kit
Model NumberLX-401301
Type20 Tests/Kit
Sensitivity98.04%,
Specificity100%
Total Accurracy> 99%
Warranty24 Months
Quality CertificationCE
Safty StandardISO13485,MSDS
Sample TypeNasal, Oropharynx Swab
Sample volume3 Full drops
Test SpeedWithin 10-15 minutes




















Product Advantage

  • Simplicity: It is extremely easy to use with simple to understand instructions.
  • Fast: After the extraction of the sample, it will take just 10-15 mins for the result to be reflected on the testing device.
  • Reliable: CE, ISO13485 Certificated, Stric quality control, High quality
  • Extraction tube is fully enclosed for disposal

Main Components

  • 20 Test Cassettes
  • 20 Sample tubes
  • 2 Sample extraction buffers
  • 20 Swabs
  • 1 Package Insert


Use Step

  • Add 550μL sample extraction (about 22-24 drops) into the sample tube.
  • Insert the swab into the sample tube prefilled with extraction buffer. Mix well and squeeze the swab 10-15 times by compressing the wall s of the tube against the swab.
  • Roll the swab head against the inner wall of the tubes as you remove it. Try to release as much liquid as possibe. Dispose of the used swab in accordance with your biohazard waste disposal protocol.
  • 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.



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).

  • INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure.




Virus Sources

Global high frequency mutationAlpha / 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,ectAlpha I B.1.17(U.K.)B.1.36.16.etc
A.2.5,etcA.23.1Alpha I B.1.17(U.K.)
B.1.1.33.etcC.1.1.etc.Others

Certificate

Application

  • Suspected population(Families and close contacts of confirmed or suspected cases)
  • High-risk groups(the elderly and children with basic illness or people with poor immunity)
  • Center for Disease Control and Prevention
  • Primary Health Care Institution

Limitations

  • This reagent is a qualitative detection reagent, which cannot determine the exact content of antigen.
  • The test results of this reagent 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

  • MOQ is ?

We have the MOQ limit, which is 10000 pieces.

  • What the certification you have?

CE, ISO9001, ISO13485

  • Delivery date?

After order confirmed, we will arrange your order immediately, and offer you an estimated delivery date.

  • Accept OEM/ODM?

Yes, we accept OEM / ODM.

  • Shipment?

Air cargo or Ocean cargo.

  • Payment Method

Business to business account.


China Rapid Nasal Oropharynx Swab COVID-19 Antigen Test Kit For Suspected Population supplier

Rapid Nasal Oropharynx Swab COVID-19 Antigen Test Kit For Suspected Population

Inquiry Cart 0