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FlowFlex OTC Rapid Antigen Test

$8.00$800.00

Exp Date: June 2025

Trusted Technology – Identical to health professional test used. This test detects multiple COVID-19 variants including the Omicron and Delta variants.

In Stock – Usually ships in 1-3 Days

 

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FlowFlex Rapid Antigen Test Kit

Exp Date: June 2025 The FlowFlex™ COVID-19 Antigen Home Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2, not for any other viruses or pathogens. Flowflex at home COVID test kit additional information:
  • For use with direct anterior nasal and nasopharyngeal swab specimens, non-invasive test procedures
  • Detects Active COVID-19 Infection - This test detects multiple COVID-19 variants including the Omicron and Delta variants.
  • Accuracy:
    • Nasal Swab: 98.8% (95% CI: 97.6%-99.5%) 95% Confidence Intervals
    • Saliva: 97.1% (95% CI: 94.6%-98.5%) 95% Confidence Intervals
  • Variant-ready solution. Detects Omricon Variant
  • Instructions for Use at Home
  • Healthcare Provider Instructions for Use
  • Fact Sheet for Healthcare Providers
  • Rapid results within 15 minutes
  • Read about the difference between Antigen tests and Antibody tests
  • Expiration Date: If you receive a box that has an expiration date that has passed, please do not be concerned. The state department has granted an extended expiration life by 12 months from the expiration date printed on the back of the box for these tests.
Please call us at 1-877-597-3224 or e-mail us at [email protected] for wholesale pricing. We are happy to provide references in theatre, government, banking, education, fortune 500 companies, and 50,000+ orders of test kits sold over the past year.
  • NO PRESCRIPTION REQUIRED - Authorized for home use.
  • TRUSTED TECHNOLOGY - Identical to health professional test used.
  • DETECTS COVID-19 INFECTION including variants.
  • NO SYMPTOMS NECESSARY – Test with or without COVID-19 symptoms.
  • QUICK-TO-TEST – Effortless test with easy-to-read results in 15 minutes.
  • EASY-TO-USE - Simple instructions and all components included.
The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner. For the most up-to-date information on COVID-19, please visit: www.cdc.gov/COVID19

DISCLAIMER

Please note that all Peach Medical shipments do not require a signature upon delivery. Since most test kits should be stored between the 35.6 and 86 degrees F range, we strongly recommend tracking your order and anticipating its delivery. However, if the test is stored outside the temperature range for a relatively short time – for a couple of hours up to a day or two – it will be fine to use as long as the test and its components are used at room temperature. Peach Medical is not responsible if the test kits are left outside in extreme temperatures for longer than the recommended time frame after delivery.

Additional information

Weight 0.09 oz
Dimensions 1.10 × 4.69 × 2.72 in
Brand

FlowflexFlowflex™

UPC

682607660261

GTIN

682607660261

MPN

L031-118B5-300

UNSPSC Code

42000000

Manufacturer

ACON Laboratories

Package Size

1 Test, 10 Tests, 100 Tests, 50 Tests

How Long Does It Take For My Item(s) To Ship?

Items are shipped Monday - Friday from our warehouse. 1-2 Day Processing Time.

Delivery times vary according to your selected delivery address, the availability of your items, and the time of day you place your order.

For B2B accounts, please get in touch with us at [email protected] for urgent order requests.

Please feel free to visit our Support Page for FDA Extension Letters, Submit a Ticket, and more.

What Shipping Methods Do You Offer?

At Peach Medical Corp we use UPS (most orders ship via UPS but some may ship via USPS) as our logistic and Shipping partners. Currently, our shipping methods are as follows:

  • UPS Next Day Air 

  • UPS 2nd Day Air

  • UPS Ground (3-5 Day Delivery)

When Will I Receive My Tracking Number?

Our system updates clients every evening with tracking numbers for their orders. This will be sent via e-mail with an additional copy of your receipt.

Incorrect Address

Please verify your address when ordering, we are unable to fix an incorrect shipping address on an order once it is in transit. If your order is in transit with an incorrect address, please reach out to your carrier to reroute the package. Peach Medical Corp. is not able to have packages rerouted or contact the carrier for you.

Refunds will not be issued for packages that were shipped to an incorrect address but it may be possible for a replacement package to be sent, please contact the customer service team to see if you are eligible.

Return Policy and Cancellation Policy

The Peach Medical COVID-19 Antigen Rapid Test and all face masks are Non-returnable & Non-refundable as they are considered personal-use items. Replacement may be shipped if the item is defective. Proof of purchase, photos of defects, lot numbers, and other information are required to authorize a replacement. Please reach out to customer service for detailed requirements before disposing of the defective units. We will not replace your COVID-19 Antigen Rapid Test kits that are expiring soon based on the printed label. Our expiration dates have been shown on each product page. More information can be found at support.peachmedical.com/portal/en/kb/peachmedicalsourcing. We will continue to update the FDA documents for shelf-life extensions for our tests.

If a customer chooses a 3rd party receiver who is not the purchaser, Peach Medical is not responsible for any goods once they leave our warehouse and when tracking is provided. I.e Gifts, International Shipping Services. All Products must be packed in the original, unopened, and unmarked packaging including any accessories, manuals, documentation, and registration that shipped with the Product.

Note: If Peach Medical has not shipped your item within 7 business days, cancellations will be honored. Please email us at [email protected] for return authorization and the shipping address.

The Flowflex COVID-19 Antigen Home Test is a rapid test for the detection of SARS-CoV-2 antigens in anterior nasal

specimens. It is intended for self-testing use. For use under an Emergency Use Authorization (EUA) only.

This test uses a nasal swab sample to determine the presence or absence of COVID-19 antigens in nasal samples. For a demonstration on how this test works, watch the instructional video.

Serial testing is a process in which a user must test themselves twice within a two-to-three-day period. The Flowflex

COVID-19 Antigen Home Test has been authorized for use as a single test by individuals with or without symptoms.

This test is authorized for nonprescription home use with self-collected (unobserved) direct anterior nasal (NS) swab

specimens from individuals aged 14 years and older or with adult-collected anterior NS samples from individuals aged

2 years or older.

This test is intended for individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.

This test is available in 2-test, 5-test, and 25-test packages.

Please do not swab your throat/ear. Please only swab your nose to collect samples and follow instructions on the package insert.

Please only use the swab that is provided with the test. Contact customer service at (800) 838-9502 for assistance.

Customer Service hours are 8 a.m. to 5 p.m. (Pacific Time), Monday - Friday.

Insert the swab ½ to ¾ inches inside your nostril. With children, the maximum depth of insertion into the nostril may

be less than ¾ of an inch, and you may need to have a second person hold the child’s head while swabbing.

Note: A false-negative result may occur if the nasal swab specimen is not properly collected

Insert the swab ½ to ¾ inches inside your nostril. With children, the maximum depth of insertion into the nostril may

be less than ¾ of an inch, and you may need to have a second person hold the child’s head while swabbing.

Note: A false-negative result may occur if the nasal swab specimen is not properly collected

Please use the swab to collect specimens from both of your nostrils to ensure sufficient sample collection to generate an accurate result.

Firmly rub the swab in a circular motion around the inside wall of the nostril 5 times. Take approximately 15

seconds to collect the specimen. Be sure to collect any nasal drainage that may be present on the swab. Repeat this in the other nostril.

14. The test cassette, extraction buffer tube, nasal swab, or tube holder is missing from the test package. What should I do?

Please contact customer service.

Monday - Friday.

Place the swab into the buffer tube and swirl for 30 seconds. Rotate the swab 5 times while squeezing the tube.

Remove the swab while squeezing the tube to extract as much liquid as possible. Attach the dropper tip firmly

onto the tube. Mix thoroughly by swirling or flicking the bottom of the tube. Then gently squeeze the tube and dispense 4 drops of solution into the Sample Well.

You should dispense 4 drops of solution into the cassette sample well. Please do not overuse the buffer solution.

You should dispense 4 drops of solution into the cassette Sample Well marked with an “S”

Results are available in 15 minutes.

No, the nasal swab is not sharp, and it should not hurt. Sometimes the swab can feel slightly uncomfortable. If you feel pain, please stop the test and seek advice from your healthcare provider.

Do not use this test on children under two years of age. Do not use this test on anyone who is prone to nosebleeds or has had facial injuries or head injuries/surgery in the past six months.

Potential risks include:

• Possible discomfort during sample collection.

• Possible incorrect test results (see Result Interpretation section).

Potential benefits include:

• The results, along with other information, can help you and your healthcare provider make informed

decisions about your care.

• The results of this test may help limit the spread of COVID-19 to your family and others in your community.

23. Is the test result still valid if I see a pinkish color on the test strip after applying the sample

to the test cassette sample well?

Pinkish background color on the test strip will not affect the result of your test.

24. What is the difference between Antigen, Molecular, and Antibody tests?

There are different kinds of tests for COVID-19. Molecular tests (also known as PCR tests) detect genetic material from

the virus. Antigen tests, such as the Flowflex COVID-19 Antigen Home Test detect proteins from the virus. Antigen tests

are very specific for the COVID-19 virus but are not as sensitive as molecular tests. This means that a positive result is

highly accurate, but a negative result does not rule out infection. If your test result is negative, you should discuss with

your healthcare provider whether an additional molecular test is necessary and if you should continue isolating at home.

Another type of test is an antibody test. A COVID-19 antibody test detects antibodies that have been produced by

your immune system in response to a previous COVID-19 infection or vaccination. Antibody tests are not suitable for diagnosing an active COVID-19 infection.

If both the control line (C) and test line (T) appear, even if the line on the test line (T) is very faint, this means that you

have a positive test result because antigens from COVID-19 were detected, and it is very likely you currently have

COVID-19. Please refer to the package insert for more information.

A positive test result means that antigens from COVID-19 were detected and it is very likely you currently have

COVID-19. There is a very small chance that this test can give a positive result that is wrong (a false-positive result).

If you test positive you should self-isolate at home per CDC recommendations to stop spreading the virus to others.

Please consult the CDC recommendations regarding self-isolation at www.cdc.gov/coronavirus. Seek follow-up care with

your healthcare provider immediately. Your healthcare provider will work with you to determine how best to care for you based on your test result(s), medical history, and symptoms.

An invalid test result indicates that not enough specimen volume was collected or incorrect test operation is the likely reasons for an invalid result. Please review the instructions again and repeat the test with a new cassette.

A false positive is a test result that indicates a person has a specific disease or condition when the person actually

does not have the disease or condition. A false-negative test result indicates a person does not have a specific disease

or condition when the person actually does have the disease or condition. Incorrect specimen collection and sample

preparation can result in false-negative and false-positive test results. Therefore, before you begin the test, it is very

important to read the package insert provided in the test package and follow the instructions.

The performance of the Flowflex COVID-19 Antigen Home Test was established in an all-comers clinical study

conducted between March 2021 and May 2021 with 172 nasal swabs self-collected or pair-collected by another

study participant from 108 individual symptomatic patients (within 7 days of onset) suspected of COVID-19 and 64

asymptomatic patients. All subjects were screened for the presence or absence of COVID-19 symptoms within two

weeks of study enrollment. The Flowflex COVID-19 Antigen Home Test was compared to an FDA authorized molecular

SARS-CoV-2 test. The Flowflex COVID-19 Antigen Home Test correctly identified 93% of positive specimens and 100% of negative specimens.

For more information on EUAs please visit: FDA Website For EUA Information

 

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