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Application: The Influenza A Rapid Test is an in vitro diagnostic test for the qualitative detection of influenza typ

Brand Name:	AllTest
Model Number:	IIN-R502
MOQ:	N/A
Price:	Negotiation
Payment Terms:	Ex works
Supply Ability:	10 M tests/month

Detail Information

Product Description

Detail Information

Place of Origin:

China

Certification:

CE, ISO13485

Format:

Cassette

Specimen:

Urine

Kit Size:

40T/Kit

Storage:

2-30℃

Color:

White

Certificate:

Packaging Details:

25 cassette/box

Supply Ability:

10 M tests/month

Highlight:

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Product Description

Convenient Accuracy And Easy Use Rapid Test Reader Influenza A+B infection Medical Product

Application:

The Influenza A+B Rapid Test Cassette (Swab/Nasal Aspirate) is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasopharyngeal swab, throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.

Description:

Influenza (commonly known as‘flu’) is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease easily transmitted through the coughing and sneezing of aerosolized droplets containing live virus.1 Influenza outbreaks occur each year during the fall and winter months. Type A viruses are typically more prevalent than type B viruses and are associated with most serious influenza epidemics, while type B infections are usually milder.

The gold standard of laboratory diagnosis is 14-day cell culture with one of a variety of cell lines that can support the growth of influenza virus.2 Cell culture has limited clinical utility, as results are obtained too late in the clinical course for effective patient intervention. Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) is a newer method that is generally more sensitive than culture with improved detection rates over culture of 2-23%.3 However, RT-PCR is expensive, complex and must be performed in specialized laboratories.

The Influenza A+B Rapid Test cassette (Swab/Nasal Aspirate) qualitatively detects the presence of Influenza A and/or Influenza B antigen in nasopharyngeal swab or throat swab or nasal aspirate specimens, providing results within 15 minutes. The test uses antibodies specific for Influenza A and Influenza B to selectively detect Influenza A and Influenza B antigen in nasopharyngeal swab, throat swab or nasal aspirate specimens.

How to use?

Allow the test cassette, specimen, extraction buffer to equilibrate to room temperature (15-30°C) prior to testing.

1.Exact QR Code from the QR code card for specific information of the test. Use only QR code card provided inside the test kits.

2.Remove the test cassette from the sealed foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed immediately after opening the foil pouch.

3.Place the Extraction Tube in the workstation. Hold the extraction reagent bottle upside down vertically. Squeeze the bottle and let the solution drop into the extraction tube freely without touching the edge of the tube. Add 10 drops of solution (Approx. 400uL) to the Extraction Tube. See illustration 1.

4. Place the swab specimen in the Extraction Tube. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the tube to release the antigen in the swab. See illustration 2.

5.Remove the swab while squeezing the swab head against the inside of the Extraction Tube as you remove it to expel as much liquid as possible from the swab. Discard the swab in accordance with your biohazard waste disposal protocol. See illustration 3.

6. Fit the dropper tip on top of the extraction tube. Place the test cassette on a clean and level surface. See illustration 4.

7. Add 3 drops of the solution (approx.120uL) to the sample well and then start the timer.

8. Wait for the colored line(s) to appear. The result should be read with AllTest™ LF Reader at 15 minutes.

9.Do not interpret test results visually.

10. For Alltest™ LF Reader installation, start up and complete instructions refer to Alltest™ LF Reader User Manual. Operator must consult the Alltest™ LF Reader User Manual prior to use and become familiar with the processes and quality control procedures.

Note: It is suggested not to use the buffer beyond 30 days after opening the vial.

INTERPRETATION OF RESULTS

Results read by AllTest TM LF reader.

The result of positive or negative for Influenza A and/or Influenza B is determined by the Alltest TM LF reader.

Result could be exported to excel or PDF.

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products details

Application: The Influenza A Rapid Test is an in vitro diagnostic test for the qualitative detection of influenza typ

Application: The Influenza A Rapid Test is an in vitro diagnostic test for the qualitative detection of influenza typ

rapid diagnostic test kits

home drug test kits