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Yes, they will. The FDA shared that the ending of the public health emergency declared by HHS under the Public Health Service Act��will not��impact FDA’s ability to authorize devices, treatments or vaccines for emergency use. Existing emergency use authorizations (EUAs) for products will remain in effect and the agency may continue to issue new EUAs going forward when criteria for issuance are met. You can learn more��.

Yes, we are. COVID-19 testing continues to be an important tool as we transition from a public health emergency to co-existing with the virus. Abbott is committed to keeping COVID-19 testing available for people to access at their doctor's office, retail pharmacy and for use at home.

Yes. We have both a lab-based test a rapid point-of-care test that can differentiate between COVID-19, flu A and B and RSV. You can learn more about our lab-based test, Alinity m,��here. And you can learn more about our rapid point-of-care test, ID NOW,��.��

Antigen tests detect proteins of the SARS-CoV-2 virus that form during the infection cycle and indicate that a person has an active infection. Rapid antigen tests offer several important benefits. They are highly portable, scalable, easy-to-use and provide a flexible approach to helping more people in more places get access to reliable testing in a cost-effective way. They are best at detecting when people are most infectious, so they know to stay home and isolate, minimizing the spread of COVID-19.

Molecular and antigen tests work in different ways to detect viruses.

Take a look at this����on how coronavirus molecular testing works. To learn how our molecular point-of-care testing on ID NOW works, see this��.

For more information on how antigen testing works, check out��this article.

Molecular tests that run on our��m2000 system have the ability to run high volumes of up to 470 tests in 24 hours. Learn more about��m2000 here:��

Alinity m systems have the ability to run high volumes of up to 1,080 tests in 24 hours. Learn more about Alinity m here:��

ID NOW delivers positive results in as little as 5 minutes and negative results in 13 minutes. Learn more about COVID-19 testing on ID NOW here:��/IDNOW.html?CID=OUS_OK����

BinaxNOW provides results in 15 minutes. Learn more about COVID-19 testing on BinaxNOW here:��/BinaxNOW-Tests-NAVICA-App.html

We have always made highly reliable and accurate tests for other infectious diseases such as HIV and hepatitis, and we're highly confident in our tests since we’ve used the same approach to development. All of our COVID-19 tests met all testing criteria under the FDA's emergency use authorization (EUA).��

Since the start of the pandemic, Abbott has produced and shipped more than 2 billion COVID-19 tests. We continue to work closely with our customers around the world to bring testing to where it’s needed most.��

Most of our tests may be available through your healthcare provider or at retail pharmacies. Our BinaxNOW Self Test is available over the counter, online and in retail stores including CVS, Walgreens and Walmart.

If you're with a hospital, lab or healthcare provider, please see the contact details below.

For general questions about BinaxNOW COVID-19 Ag Card:��

For general questions about ID NOW:����

For general questions about��m2000:��

For general questions about ARCHITECT:��

For general questions about Alinity i:��

For general questions about Alinity m:��

The FDA has made tests available under an emergency access mechanism called an Emergency Use Authorization (EUA). The EUA is supported by the Secretary of Health and Human Services' declaration that circumstances exist to justify the development of in vitro diagnostics (IVDs) under EUA for the detection and/or diagnosis of 2019-nCoV. Click here for more info:��

Please check the CDC resources on how to protect yourself and what to do if you think you are sick:��

The FDA granted approval for a 22-month shelf-life extension for our Self Tests. You can double check the expiration date of the tests you have on hand via our , so you know you’re getting the most reliable results.��

Here’s how to check the expiration date of your test:

1. Find the expiration date on the box. First, find the sticker on the bottom right-hand corner on the back of the box. Next to the hourglass symbol, you’ll see the listed expiration date. If the date has already passed, continue to Steps 2 and 3 to see if the expiration date has been extended by the FDA.

   

2. Find the lot number on the box. The lot number is beneath the expiration date, next to the letters “LOT.”

   

3. Search the lot number to find the expiration date extension. Input your lot number via our at rapidtest.abbott/binaxnow to confirm the expiration date extension of your test.

Reminders:

• Finding the lot number is most important. If your test’s lot number appears, trust the extended expiration date, even if the printed expiration date doesn’t match.
• If your test’s lot number doesn’t appear, the test’s expiration date may not have been extended. You can recycle the box, but should dispose of the test card, nasal swab and test solution in common household waste, in line with the test’s instructions for use.

Learn more about Abbott's approach to tackling the coronavirus:��
Read more about ARCHITECT:��
Read more about ID NOW:��/IDNOW.html
Read more about��m2000:��
Read more about Alinity i:��
Read more about Alinity m:��
Read more about��BinaxNOW COVID-19 Ag Card:��

Learn more about Abbott's approach to tackling the coronavirus:
Read more about ARCHITECT:
Read more about ID NOW:��
Read more about m2000:
Read more about Alinity i:
Read more about Alinity m:
Read more about BinaxNOW COVID-19 Ag Card:��