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Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests

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Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests
Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests

Large Image :  Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests

Product Details:
Place of Origin: China
Brand Name: LABNOVATION
Certification: ISO13485, ISO9001, CE
Model Number: LX-401401
Payment & Shipping Terms:
Minimum Order Quantity: 10000
Price: US$0.9-2/Pcs
Packaging Details: Carton
Delivery Time: 5-7 work day
Payment Terms: D/A, D/P, T/T
Supply Ability: 500000/Day

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests

Description
Storage: 2℃-30℃ Warranty: 18 Months
Test Speed: Within 15-20minutes Certification: ISO13485, ISO9001, CE
Freeze: Not Allowed Sunshine: Avoided
Total Accuracy: >90% Humidity: ≤60%
High Light:

Professional Influenza AB Test Kit

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Influenza AB Test Kit 20 Tests

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CoV 19 Antigen flu swab kit

Rapid Test Kit CoV-19 Antigen And Influenza A/B Rapid Test Kit 20 Tests Professional Rapid Test Kit

 

Intended Use

SARS-CoV-2 antigen & influenza A/B rapid test kit provide a simple, rapid detection as an aid in the differential diagnosisi of SARS-CoV-2 antigen and influenza A/B using nasal swab specimens. This easy-to-use product and rapid results can be used for the screeningof early infected patients and asymptomatic patients. It is also effective supplement for nucleic acid detection.

Specification

Item

Antigen test strip performance

against PCR

Influenza A test strip performance against PCR Influenza B test strip performance against PCR
Sensitivity 98.03% 93.3% 97.00%
Specificity 100.00% 91.00% 96.40%

Main Components

  • Test cassettes
  • Sample extraction Buffer
  • Sample tubes
  • Swabs
  • Tube Stand
  • Instruction For Use

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests 0

 

Use  Step

  • Take out the test cassette from the sealed pouch, place it on a clean and level surface with the sample port well up.
  • Apply 2 full drops of the treated sample (60μl-70μl) vertically into each of the two sample wells of the test cassette.

  • Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests 1

 

Interpretation Of Result

  • POSITIVE: The presence of T (T on nCoV /A or B on Flu) and C lines within the reaction window indicate a positive result on SARS-CoV-2 or Flu A and/or B infection or co-infection.

  • NEGATIVE: One colored line appears in the control region(C). No apparent colored line appears in the test region (T on nCoV /A or B on Flu). 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.

 

 

 

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests 2

 

Feature

  • Non-invasive
  • Simple to use
  • Convenient, no devices required
  • Rapid, get result in 15 minutes
  • Stable, with high accuracy
  • Inexpensive, cost-efficiency

 

 

Professional CoV-19 Antigen Influenza AB Test Kit 20 Tests 3

Storage and Expiry

Store as packaged in the sealed pouch at 2-30℃, avoid hot and sunshine, dry place, valid for 12 months. Do not freeze. Some protective measures should be taken in hot summer and cold winter to avoid high temperature or freeze-thaw. Do not open the inner packaging until ready, it must be used in one hour if opened (Humidity≤60%, Temp: 20℃-30℃). Please use immediately when the humidity>60%

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

  •  About MOQ?

Usually is 10000pcs, we would like to cooperate with you, don't worry about MOQ, just send us of the items you want to order.

  • Accept ODM/OEM?

Yes, we're manufacturer. OEM/ODM is accepted.

  • The Shipment?

AIR Cargo, Ocean Cargo or others, you can choose any one which is convenient for you.

  • Payment Method

Business to business account.

 

  • Delivery date?

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

 

 

 

 

Contact Details
Labnovation Technologies, Inc.

Contact Person: Ld

Tel: +8613480985156

Send your inquiry directly to us (0 / 3000)