Influenza A/B Rapid Test Kit (FIA) - Vitrosens Biotechnology
Influenza A/B Rapid Test Kit (FIA)

Information

This test kit is designed for identification both Influenza A and B viral nucleoprotein antigens in human nasopharyngeal samples. Automated results are ready within only minutes.

Influenza A/B Rapid Test Kit (FIA)

Advantages

  • 2in1 test for both influenza A and B
  • Simple procedure
  • Automated interpretation
  • Minimized human errors
  • Maximized accuracy and sensitivity

How To Use
Influenza A/B Rapid Test Kit (FIA)

Sampling

Sampling 1

1.Take blood from the arm to a sterile tube. Centrifuge the tube filled with blood. By using a plastic dropper, take 1 drop serum sample.

Sampling 2

2. Take blood from the arm to a sterile tube. Centrifuge the tube filled with blood. By using a plastic dropper, take 1 drop plasma sample.

Sampling 3

3. Take blood from the arm to a sterile tube. By using a plastic dropper, take 1 drop blood sample or gently prick the tip of the finger and By using a plastic dropper, take 1 drop blood sample.

Procedure

Procedure 1

1. Add one drop of specimen to the sample (S) well.

Procedure 2

2. Open the extraction buffer tube.

Procedure 3

3. Add two drops of extraction buffer to the diluent (D) well.

Procedure 4

4. Turn on the device. Place the ID chip to the ID chip port. Read the cassette.

Interpretation of the Result
Influenza A/B Rapid Test Kit (FIA)

This product can only perform qualitative analysis on the detection object.

A/B Positive Result: If both C, A and B lines are visible within 10 minutes, the test result is positive and valid.
A Positive Result: If both C and A lines are visible within 10 minutes, the test result is positive and valid.
B Positive Result: If both C and B lines are visible within 10 minutes, the test result is positive and valid.
Negative Result: If test area (A and B lines) has no color and the control area displays a colored line, the result is negative and valid.
Invalid Result:The test result is invalid if a colored line does not form in the control region. The sample must be re-tested, using a new test cassette.

Interpretation of the Result
Influenza A/B Rapid Test Kit (FIA)

This product can only perform qualitative analysis on the detection object.

A/B Positive Result: If both C, A and B lines are visible within 10 minutes, the test result is positive and valid.
A Positive Result: If both C and A lines are visible within 10 minutes, the test result is positive and valid.
B Positive Result: If both C and B lines are visible within 10 minutes, the test result is positive and valid.
Negative Result: If test area (A and B lines) has no color and the control area displays a colored line, the result is negative and valid.
Invalid Result:The test result is invalid if a colored line does not form in the control region. The sample must be re-tested, using a new test cassette.

Influenza A/B Rapid Test Kit (FIA)
Usage Video

Certifications
Influenza A/B Rapid Test Kit (FIA)

Our test kits are prepared according to the following standards.
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Box Content
Influenza A/B Rapid Test Kit (FIA)

Content 25 Test Option
ID Card 1 Pc.
Test Cassette 25 Pcs.
Extraction Buffer  1 Pc.
User Manual 1 Pc.

Frequently Asked Questions
Influenza A/B Rapid Test Kit (FIA)

How accurate is RapidFor™ Rapid IgG/IgM Test Kit?

RapidFor™ Rapid IgG/IgM Test Kit has been shown to have greater than 95% accuracy in clinical trials. Please refer to the “Instruction for Use (IFU)” for more details.

Does RapidFor™ Rapid IgG/IgM Test Kit harmful?

When you pierce your finger, you should be cautious. You should not go any further. The goal of this step is to get a little amount of blood enough for the antibody-detection. If you feel any discomfort, stop the procedure, and seek medical help.

Will RapidFor™ Rapid IgG/IgM Test tell me if I have been infected with COVID-19 in the past?

Yes, if your test result is positive for only IgG antibody (appears in the blood approximately 2-3 weeks after onset of symptoms) which can remain in the blood and ensure long-term immunity against SARS-CoV-2 (COVID-19); that means you have been infected with COVID-19 in the past. IgM antibodies (appear in the blood approximately 5-8 days after onset of symptoms) reveal an early immune response  to SARS-CoV-2, indicating that you are at the beginning of the infection.

What do I need pay attention when performing RapidFor™ Rapid IgG/IgM Test Kit?

Please read the instruction manual thoroughly before taking the test. After removing the test cassette from the foil wrapper, the procedure should be finished in 15 minutes. After usage, recap the buffer solution as soon as feasible.  Samples should be obtained using standard clinical procedures and avoid hemolysis. Samples with obvious hemolysis, lipohemia, or jaundice should not be utilized. The samples should be utilized as soon as possible after being collected (within half an hour).

How could I act if I get positive test result?

Make contact with your healthcare professional and let them know about your condition. A polymerase chain reaction (PCR Test) test should be used to confirm the presence of COVID-19 infection. If the illness is confirmed, you should isolate yourself and follow your local public health regulations. Inform your coworkers and others you met in the last two weeks during your self-isolation.

How could I act if I get negative test result?

Our tests provide high accuracy however, you could not be sure totally. The test detects IgG and IgM antibodies produced by your body; in the early stage of SARS-CoV-2, these antibodies may not be produced by your body enough that the test detect so you should have another test after 4-5 days. Do not forget to maintain social distancing and to avoid risky areas.

Is the test cassette being reusable?

Absolutely not; the test cassette is intended to be used just once. It is strongly advised against testing another sample with the same cassette.

How can I dispose of the test after I use it?

Put everything you use into aluminum foil again, especially lancets. Lancets (the tool with which you puncture your finger) can injure you and spread blood-borne infections. With your blood sample, return all used and unused lancets. Place lancets in the trash, not the recycling bin. Keep animals and kids out of reach. Dispose all the materials used during the test to biological waste if you have access to one.

How and how long can I store RapidFor™ Rapid IgG/IgM Test Kit?

Store in a sealed bag between 2°C and 30°C until the expiration date on the packaging is reached; do not store below 2°C or consume expired products. The label has the MFG and EXP dates written on it. The product will be unavailable to use after 24 months.

Order Information
Influenza A/B Rapid Test Kit (FIA)

Cat No. Name Specimen Kit size CE Status
VMPO58 Influenza A/B Rapid Test Kit (FIA) NP 25 T

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SARS-CoV-2 Antigen Rapid Test Kit, COVID-19 Test Manufacturer.
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SARS-CoV-2 Antigen Rapid Test Kit, COVID-19 Test Manufacturer.
vitrosens.com
InternationalPresence
Follow USVITROSENS on Social Media
For our updated news and products follow us on social media.

Copyright by Vitrosens Biotechnology. All rights reserved.

Copyright by Vitrosens Biotechnology. All rights reserved.