Accula SARS-CoV-2 Test

Everything about Accula SARS-CoV-2 Test

In times like the epidemic, we are hesitant to go out for a test whenever we feel like having symptoms similar to COVID-19 infection. That is where the Accula SARS-CoV-2 test falls in.

The Accula SARS-CoV-2 test is a diagnostic test that uses PCR and lateral flow technologies to detect the presence of the virus that causes COVID-19 in nasal or nasal mid-turbinate swab specimens. It combines RT-PCR precision with a straightforward procedure to deliver PCR-based test conclusions quickly and conveniently.

First of all, a Polymerase Chain Reaction (PCR) test is a widely used method to detect small quantities of DNA specific to a pathogenic agent like the SARS-CoV-2 virus, in blood or any other body fluids.

Similarly, the Lateral Flow Test is a rapid antigen analysis that uses samples from your throat or nose to identify the protein markers existing on the surface of the SARS-CoV-2 virus in less amount of time than laboratory trials.

In the same way, the Accula SARS-CoV-2 test utilizes upper respiratory specimens in a sample collection device which is then placed into a dock, where PCR amplification and lateral flow detection occur. It is a rapid and sensitive measure designed to be used in point-of-care settings, meaning it’s collected on-site and only administered by a healthcare professional.

Moreover, it provides outcomes in as little as 15 minutes and is easy to use with minimal training required for administration.

Furthermore, in the article, we shall divulge the Accula SARS-CoV-2 test’s availability, price, accuracy, authenticity, instructions to use, and why you should choose the test.

Accula SARS-CoV-2 Test Price & Availability

As the Accula SARS-CoV-2 is a POC test, an individual without any medical personnel prescription can not simply acquire the testing tool. You can not merely purchase a POC test and apply it by yourself without supervision. But that does not imply the tool is unavailable.

The Accula SARS-CoV-2 test is allowed to be marketed in most parts of the world. You may effortlessly procure the product if you have medical permission. Or, if you reside in a remote place without a nearby testing facility, you can purchase the Accula SARS-CoV-2 test and ask the pharmacist to do the swab check.

Likewise, if available in your area, you can order the tools online and request your neighboring healthcare specialist to examine you.

Besides that, we also deal in medical products such as rapid test kits. You can contact us through email or the subscription form and get the Accula SARS-CoV-2 test or other test kits at a fair cost.

SVI Medical Group works closely with the manufacturers and globally distributes antigen medical supplies like antigen test kits, nitrile gloves, PPE kits, etc. at the most reasonable price. Do not hesitate. Place your order of any amount (a few or in bulk).

Is the Accula SARS-CoV-2 Test Accurate?

Generally, a POC test like the Accula SARS-CoV-2 test determines the Coronavirus pathogens at least 95% of the time when someone is infected. Plus, point-of-care trials are performed at a specific facility by clinical experts, so evidently, they are likely to be more accurate than other forms of rapid tests.

Moreover, the test has been designed to minimize the likelihood of false positive results. However, it is still possible that this test can give false positive results. In a retrospective specimen study, the Accula SARS-CoV-2 test achieved 95.8% positive and 98% negative percent agreement with a EUA-authorized RT-PCR SARS-CoV-2 trial.

Therefore, you should consult a doctor or take a PCR test on the condition that your symptoms still prevail after taking the Accula COVID test and getting a negative conclusion.

Is the Accula SARS-CoV-2 test FDA Approved?

The Accula SARS-CoV-2 test has not been FDA-cleared or approved but has been authorized for emergency use by the United States Food and Drug Administration(FDA) under an Emergency Use Authorization(EUA) by authorized laboratories. Also, the test has been authorized only for detecting nucleic acid from SARS-CoV-2, not for any other viruses or pathogens.

It is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of test tube diagnostics for the detection and/or diagnosis of COVID-19.

Why should you choose Accula SARS-CoV-2 Test?

Point-of-care tests have their own advantages over home tests. Like self-tests, the Accula SARS-CoV-2 test is too greatly reliable, efficient, and provides fast results. Some of the other points for why you should choose the Accula SARS-CoV-2 test are discussed below.

Easy to Use: The Accula test is simple to perform and does not require laboratory facilities to deduce results, making it suitable to use in every possible setting, including at home.

Cost-effective: Generally, POC tests are designed to imply to a large number of people, hence, the Accula SARS-CoV-2 test is available at a budget-friendly price globally around the world.

Accessibility: Besides that, the Accula SARS-CoV-2 test is FDA-approved and accepted by other nations’ medicinal departments. Therefore, you can find this test all around the world and a medical licensed person can easily purchase and administer it.

Quick Outcomes: A POC test is more swift and accurate than home tests, and does not require long hours like in laboratory tests. So, with the Accula test, you will get the results as quickly as 10 minutes.

High Accuracy: The Accula SARS-CoV-2 test is composed of PCR and lateral flow, meaning it is a designed POC test to get more accurate and sensitive results. Moreover, it is administered by a healthcare expert, hence, lessening the chances to get false positive outcomes.

Non-invasive:  Accula test is non-invasive, concluding that it does not require a blood sample to test out the infection. Which eventually reduces the risk of further contamination.

Accula SARS-CoV-2 Instructions for Use

The Accula SARS-CoV-2 test is conducted in certain trial facilities by trained medical professionals sanctioned by the authoritative health commission. But, under the direct monitoring of a trained healthcare expert, that implies anyone with proper medical training, an individual can follow the procedure provided in the instructions book.

So, here is the instruction that you must carry out to perform a successful rapid test.

NOTE: Store reagents at room temperature (59°F to 86°F). Also, do not refrigerate or freeze, and do not reuse kit contents such as Collection Swabs, Test Cassettes, and Transfer Pipettes.

STEP 1: First of all, sanitize your hands with a potent sanitizer or wash your hands with a bar of soap for at least 1 minute. And remove the swab from the package without touching the head of the swab.

STEP 2: Then tilt the patient’s head back 70 degrees and gently insert the soft end into your nostril with a flexible shaft (wire or plastic) until resistance is encountered, indicating contact with the nasopharynx.

STEP 3: Tenderly rub and rotate the swab pressing gently against the insides of your nostril. Now, leave the swab in place for several seconds and get as much nasal discharge as possible.

STEP 4: Slowly remove the swab while rotating it and repeat the previous process in your other nostril without replacing the swab. But collection from both nostrils is unnecessary if the swab is saturated enough.

NOTE: If a deviated septum or difficulty in collecting a specimen occurs, use the same swab to obtain a specimen from the other nostril.

STEP 5: Tear off the seal on top of the buffer tube, and insert the accumulated nasal swab specimen directly into the SARS-CoV-2 Buffer Solution tube immediately.

STEP 6: Before removing the swab, rotate it at least 5 times or for at least 10 seconds rubbing it against the wall of the vial. 

STEP 7: Remove the swab from the tube while squeezing it against the inside of the tube to expel as much liquid as possible from the swab.

NOTE: If the buffer solution contacts the skin, wash the area with soap and clean water and rinse thoroughly. Consult a physician if irritation develops.

STEP 8: After that, tighten the cap of the extraction buffer tube and remove the Dock from the sealed pouch and place it on a flat surface.

STEP 9: Now, connect the power cord to the Dock and plug the AC end into an electrical outlet. And open the Dock by depressing the black button located on the top left and verify the screen display “DOCK READY INSERT CASSETTE”.

STEP 10: Remove a Test Cassette and a Transfer Pipette from the foil package and insert the Test Cassette into the Dock, leaving the lid open. Then, firmly press the Cassette to seat into the Dock.

NOTE: Verify the Dock screen displays: “SARS-COV-2 CASS. INSERTED”. The Dock screen will then display: “ADD SAMPLE THEN CLOSE LID”.

STEP 11: Invert the SARS-CoV-2 Buffer vial to mix and firmly squeeze the top bulb of the Pipette below the surface of the liquid of the vial containing the eluted patient sample.

STEP 12: Slowly release the top bulb to completely fill the Pipette stem with the sample.

STEP 13: Completely remove the foil tab covering the sample port on the Test Cassette. And insert the tip of the Pipette all the way into the sample port of the Test Cassette until resistance is met.

STEP 14: Squeeze the top bulb of the Pipette firmly to dispense all of the samples from the stem into the Test Cassette.

NOTE: Along steps 11 to 14, a small amount of sample, excess liquid, may remain in the overflow chamber (lower bulb) which is totally normal.

STEP 15: Close the lid of the Dock quickly and verify the Dock screen display: “SAMPLE LOADED LID CLOSED”, and then, “CASSETTE SEALED TEST STARTED” with the last message “TEST RUNNING REMAINING XX: XX”.

The test then takes approximately 10-30 minutes to complete. After the processing has been completed, the Dock will beep and display “TEST COMPLETE READ RESULTS”.

Finally, open the lid of the Dock, remove the Test Cassette, and interpret the results accordingly.

How to determine the result?

  • The appearance of any shade of a Blue Line at the T position, with or without appearing at the C position, along with the absence of a negative line at the NC position, verifies the result as POSITIVE.
  • Along with the presence of a Blue Process Control Line at the C position and the absence of any shade at the T and the NC position indicates a NEGATIVE result for the presence of SARS-CoV-2.
  • Likewise, the trial is considered INVALID if any appearances occur at the NC position. Also, the appearance of ALL or NO lines at the C, T, and NC position implies an INVALID test.


Overall, the Accula SARS-CoV-2 test is a highly efficient and accurate method for detecting the presence of the novel coronavirus. With its quick and simple administration process, it provides results in under an hour, making it a valuable tool for controlling the spread of COVID-19.

It is what you are looking for. Its high sensitivity and specificity, combined with its ease of use, make it a reliable option for individuals and healthcare providers alike. That is why we recommend you use the test and be sure whether your symptoms are similar to the seasonal flu, common cold, or COVID-19.

Furthermore, if you want to know more about similar rapid antigen test kits, be sure to check our blog. Also, feel free to comment on the articles, we highly appreciate your support.

Share the articles with your friends and relatives on social media, and let them know more about COVID infection and their test methods.


What is Accula Test?

Accula Test or Accula SARS-CoV-2 test is a specifically designed POC test, combined with PCR and lateral flow, to detect the virus that causes COVID-19 in anterior nasal swab specimens.

Is the SARS-CoV-2 Test Accurate?

Molecular (PCR) tests for SARS-CoV-2 have high sensitivity, typically greater than 95% when performed correctly. However, antigen tests or at-home tests normally detect the SARS-CoV-2 virus in around 80% of infected individuals.