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RapidFor™ SARS-CoV-2 & FLU A/B Combo Antigen Test Kit uses the colloidal label as a tool to detect the SARS-CoV-2 antigen test and the FLU A/B antigen detection in the collected nasopharyngeal and nasal swab specimens.
– Easy to use and read
– 2 in 1 test for Influenza and SARS-CoV-2
– No extra lab equipment
– Variant Detection [B.1.1.7 (Alpha), B.1.351 (Beta), E484K mutation,
B1.617.2 (Delta), P.1 (Gamma), C.37 (Lambda), B.1.1.529 (Omicron)]
– Early phase detection
– Suitable for rapid screening a large number of people
– Test Cassette
– Extraction Buffer
– Holder (Optional)
– User Manual
|Intended use||Detection of SARS-CoV-2 antigen|
|Storage||2-30℃ / 35.6-86℉|
|Specimen type||Nasal swab|
|Time to result||15 minutes|
|Shelf life||24 months|
|Sensitivity Influenza A||97.44%|
|Specificity Influenza A||99.47%|
|Sensitivity Influenza B||96.97%|
|Specificity Influenza B||99.21%|
|Sensitivity Cov-19 Ag||97.3%|
|Specificity Cov-19 Ag||99.05%|
If you have symptoms of COVID-19 and you cannot sure whether you have SARS-CoV-2 or influenza, RapidFor™ SARS-CoV-2 & FLU A/B Combo Antigen Test Kit is here for you. With RapidFor™ Flu A/B Rapid Antigen Test Kit, you can monitor for both influenza and SARS-CoV-2 antigens. COVID-19, a respiratory infection caused by the new coronavirus SARS-CoV-2, has symptoms that are easily mistaken for influenza. Because COVID-19 is a reportable disease, it is critical that a patient with severe disease symptoms such as fever, dry cough, sore throat, headache, joint pain, and weariness has a definitive diagnosis as soon as feasible.
Although both viruses cause respiratory illness, there are significant variations in how they propagate. This has significant consequences for the public health actions that may be taken in response to each virus, as well as how fast a patient’s treatment is determined in order to avoid severe sickness or death.
RapidFor™ SARS-CoV-2 & FLU A/B Combo Antigen Test Kit has an accuracy rate more than 95%, according to clinical trials. Please read the “Instruction for Use (IFU)” for further details.
Yes, the test is capable of detecting the virus at an early stage (2-4 days after viral exposure). Please see the section “Test Types Comparison” for further information.
COVID-19 viral mutations are being actively monitored by the RapidFor™ SARS-CoV-2 & FLU A/B Combo Antigen Test Kit, as we do with many viruses, to guarantee that our tests can detect them. We’ve done a thorough examination of the current variants including B.1.1.7 UK (Alpha), B.1.351 South Africa (Beta), E484K mutation, B1.617.2 India (Delta), P.1 Brazil (Gamma), C.37 (Lambda); that we have seen, and we are certain that our tests will still detect these strains. The test looks for proteins that the COVID-19 virus needs to stay alive.
In comparison with the Real-Time Polymerase Chain Reaction Test (RT- PCR Test), RapidFor™ SARS-CoV-2 & FLU A/B Combo Antigen Test Kit enables us to screen the existence of the illness of concern in a very short time. This benefit gives us the opportunity to test more people in less time. It is a major advantage in the event of worldwide pandemics such as COVID-19. Since many of the COVID-19 symptoms are similar to those associated with common cold, or other diseases, the testing of a person having or not COVID-19 is required.
When you insert the end of the nasopharyngeal swab into your nose, it should not harm you because it is not sharp. We provide a simplified sample; just 2.5 cm should be smeared in the nostrils. From time to time, the swab may be uncomfortable. If you get uncomfortable during the test, stop it and seek medical help.
If you get positive results for influenza, get an appointment from your healthcare provider to get further diagnosing.
Contact your healthcare practitioner and explain your circumstances. You should get polymerase chain reaction (PCR Test) 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 meet in two weeks about your self-isolation.
Please read the instruction manual thoroughly before doing the test. After removing the test cassette from the foil wrapper, the process should be finished within 15 minutes. After usage, the buffer solution should be recapped as soon as feasible. The samples should be utilized as soon as possible after being collected (within half an hour). Inactivation of samples is not permitted.
No, the test cassette is intended for single use only. It is strongly advised not to use the same cassette to test another sample.
Store in a sealed bag at 2°C to 30°C until the expiration date on the box; do not store below 2°C and do not use expired products. The label bears the MFG and EXP dates. The product will no longer be available for usage after 24 months.
Our tests are highly accurate, but you cannot be completely certain. Because the viral load in your body may not be significant enough for the test to identify, you should undergo another test in 4-5 days. Remember to maintain social distance and avoid risky situations.
Fill the aluminum foil with everything you’ll need for the process, including the swab, tube, and test cassette. Put them in the garbage can, not the recycling bin. Keep pets and children out of reach. If you have access to one, dispose of all items used during the test in biological waste.