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Labnovation Technologies, Inc.

  • China,Shenzhen
  • Active Member

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China Diagostic Use SARS-CoV-2 Antigen Rapid Test Kit High Accuracy For Home
China Diagostic Use SARS-CoV-2 Antigen Rapid Test Kit High Accuracy For Home

  1. China Diagostic Use SARS-CoV-2 Antigen Rapid Test Kit High Accuracy For Home

Diagostic Use SARS-CoV-2 Antigen Rapid Test Kit High Accuracy For Home

  1. MOQ: 10000 Pieces
  2. Price: Negotiation
  3. Get Latest Price
Payment Terms T/T, D/A, D/P
Supply Ability 500000/Day
Delivery Time 5-7 work day
Packaging Details Carton
Quanlity Guarantee Period 24 months
Storage Condition 2-30℃
Test Time Within 15 min
Package 20 Tests/Kit
Type IVD Reagent Test Kit
Group Universal
Brand Name LABNOVATION
Model Number LX-401301
Certification ISO13485,ISO9001,CE
Place of Origin China

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  1. Product Details
  2. Company Details

Product Specification

Payment Terms T/T, D/A, D/P Supply Ability 500000/Day
Delivery Time 5-7 work day Packaging Details Carton
Quanlity Guarantee Period 24 months Storage Condition 2-30℃
Test Time Within 15 min Package 20 Tests/Kit
Type IVD Reagent Test Kit Group Universal
Brand Name LABNOVATION Model Number LX-401301
Certification ISO13485,ISO9001,CE Place of Origin China
High Light IVD Antigen Rapid Test KitHigh Accuracy Antigen Rapid Test KitDiagostic SARS-CoV-2 home antigen test kit

Rapid Antigen Test Kit Professsional Diagostic Use SARS-CoV-2 Antigen Rapid Test Kit CE Certificated High Accuracy

 
Intend Use

The Labnovation SARS-CoV-2 antigen 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.

Product Details

Item Value
Test Item SARS-CoV-2 Antigen Rapid Test Kit
Type 20 Tests/Kit
Warranty 24 Months
Quality Certification CE
Safty Standard ISO13485
Sample Type nasopharyngeal  / oropharyngeal 
Test Speed Within 15 minutes
Sample Volume 3 full drops

 
Main Components

  • Test Cassettes
  • Sample tubes with Prefilled Sample extraction buffer
  • Swabs
  • Tube Stand
  • Instruction for use


Analytical Results

SARS-CoV-2 Antigen Rapid Test Kit
Sensitivity Specificity Total accuracy
98.04% 100.00% 99.60%

 
Product Features

  • High Accuracy, Sensitivity and specificity
  • Detection of mutations
  • Safety and reliability
  • Simple Operation, No extra instrument
  • Results in 15 minutes and easy to read

Use Step

  1. 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.
  2. 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.
  3. 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. Omicron

 

Limitations

1. This reagent is a qualitative detection reagent, which cannot determine the exact content of antigen.

2. 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.

3. 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.

4.False negative results may be caused by unreasonable sample collection, transport and treatment, and low viral load in samples.

 

Certificate

 
 
 

Company Details

Bronze Gleitlager

,

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 and 

Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer

  • Year Established:

    2001

  • Total Annual:

    10000000-50000000

  • Employee Number:

    100~600

  • Ecer Certification:

    Active Member

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 reagent... 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 reagent...

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Get in touch with us

  • Reach Us
  • Labnovation Technologies, Inc.
  • 101 and 5th Floor, Building 1, No. 68,18th Road, Guangming Hi-Tech Park, Tangjia Community, Fenghuang Street, Guangming District, Shenzhen 518107 ,China
  • https://www.labnovationtest.com/

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