Low 33F. This test is used on our ID NOW instrument. 0000126497 00000 n hbbd``b`$gfD\@m`m,N Dp~! 0000019899 00000 n 0000105677 00000 n But be aware that with the COVID antigen tests, the expiration date may be a moving target. OraSure Technologies, Inc.: InteliSwab COVID-19 Rapid Test 9-month to 12-month self-life extension granted by the FDA August 3, 2022 Lot Number Tests with this printed expiration date (Year-month-day) D 0000007821 00000 n 0000152529 00000 n Your e-mail address will be used to confirm your account. 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. 0000105492 00000 n Also, our manufacturer will NOT supply to any other organizations in the U.S. except for iHealth Labs Inc. It may seem obvious, but read the instructions. Both components, the reagent and the antibodies, start to degrade at some point, Pettengill said. hXnF}L @[ X"@)]JiZB 0000007689 00000 n ]bqi"w8=8YWf8}3aK txg^+v!a{Bhk 5YliFeT?}YV-xBmN(}H)&,# o0 agr. endstream endobj 110 0 obj <>/Metadata 6 0 R/PageLayout/OneColumn/Pages 5 0 R/StructTreeRoot 8 0 R/Type/Catalog>> endobj 111 0 obj <>/Font<>/XObject<>>>/Rotate 0/StructParents 0/Type/Page>> endobj 112 0 obj <> endobj 113 0 obj <> endobj 114 0 obj <> endobj 115 0 obj <> endobj 116 0 obj <> endobj 117 0 obj [139 0 R] endobj 118 0 obj <>stream :yt8t$6;-lFh -/WG]w;Z]uN % Use the instructions to see the letter and listing of BinaxNOW COVID-19 Ag Card lots which qualify for this expiry extension. :yt8t$6;-lFh -/WG]w;Z]uN What if packages are exposed to temperatures outside those ranges for short periods, such as during shipping? Submitting this form below will send a message to your email with a link to change your password. IS THERE ANY RISK OF CONTAMINATION FOR LAB WORKERS WHO ARE OPERATING ID NOW? It is used on our ID NOW platform. Please be aware that the website you have requested is intended for the residents of a particular country or region, as noted on that site. We created a Global Surveillance Program 25 years ago to monitor HIV and hepatitis viruses and have a long-standing discovery program to identify new or unknown pathogens. expiration date (Year-Month-Day) Abbott Diagnostics Scarborough, Inc.: BinaxNOW COVID-19 Ag Self Test 15-month to 22-month shelf-life extension granted by the FDA December 21, 2022 0000126767 00000 n Clinicians and lab professionals have been using the same ID NOW instrument, collection swabs, and consumables (such as the sample receiver and transfer cartridge) to safely test respiratory viruses during this time. 0000001804 00000 n Click here for more info: https://abbo.tt/2X7xwZo, Please check the CDC resources on how to protect yourself and what to do if you think you are sick: https://abbo.tt/3hJSINd, Learn more about Abbott's approach to tackling the coronavirus: https://abbo.tt/2WHMDco 0000006042 00000 n 0000005193 00000 n All three versions of the test pair with our optional mobile app foriPhoneandAndroiddevices, NAVICATM. H\j0~ They are not all the same, and they can be confusing. Press release announcing launch of the ID NOW COVID-19 test here. Make sure youre looking at the expiration date. endstream endobj 162 0 obj <>stream HOW DO I KNOW IF I NEED TO SEEK OUT ONE OF YOUR TESTS? But the manufacturer, Abbott, obtained a three-month extension on the expiration date after supplying additional data to the FDA. Results may be delivered in 13 minutes or less. Ourm2000 and Alinity m molecular systems are used in hospital and lab settings that are testing high volumes. Abbott is providing these links to you only as a convenience, and the inclusion of any link does not imply endorsement of the linked site by Abbott. 0000014860 00000 n :C1lr"wiUog-+Wu4W_*_EVqX~/,Lgj>Am=1-ij [)l+vr}H\b5&k?~s?YJgX?9n/t(8,?zzIc^|vxH>_{$HH>X{F)"y$sDmA=Jd:"'Vvu;;iX[g Learn more about COVID-19 testing on ID NOW here:https://abbo.tt/3KI9smQ, BinaxNOW provides results in 15 minutes. The test does not need any additional equipment. Learn more about COVID-19 testing on BinaxNOW here:https://abbo.tt/3hZPfNx, Our serology tests on the ARCHITECT and Alinity i systems can run up to 100-200 tests per hour. H\j >w%PrNReby6l*s)do@q;@. 0000075543 00000 n Read more about m2000: https://abbo.tt/2U1WMiU 3077 0 obj <> endobj Our antibody and molecular lab tests are available around the world, as well as our ID NOW rapid molecular test. We, iHealth Labs Inc, hereby clarify that we and our authorized distributors are the only organizations in the U.S. that may legally sell and distribute the Kit under FDA EUA. These tests have not been FDA cleared or approved. 0000001630 00000 n Expiration Date Extension by Dingchao Liao February 13, 2023 On Jan 11, 2023, the FDA granted another three-month shelf-life extension for the iHealth COVID-19 Antigen Rapid Test, which extended the shelf-life of all iHealth tests from 6 months to 15 months. hUYo8+|LPdy"PQ;^4G]yPlIY~gH9mXo|r # b4I LeHCG%F>!V 8{.4 cXXD!08En5.JQ(NFE}LzZVy9;? HOW DO YOU PERFORM AN ID NOW COVID-19 TEST? This test is used on our ID NOW instrument. The ID NOW COVID-19 test is a rapid, molecular point-of-care test that detects COVID-19 in 13 minutes or less. If you forget it, you'll be able to recover it using your email address. We have developed twelve tests for COVID-19 globally. h2T0Pw/+Q0L)67 We have always made highly reliable and accurate tests for other infectious diseases such as HIV and hepatitis, and we're highly confident in our tests since weve used the same approach to development. Check out our most recent progress update here. 0000105562 00000 n Fx J+-'[^(0V*JCIZ$V.$?gS,|6 FgRQ4:Gh#^zKgmyE1VQz^}[|(>wiqp_wWPOztK=z|1w|35_,NK#uYapFYsr2V)o;lQi9}w|1IY\6v0Ok!o+E./8? /[&%x~@!O'6)1"42qY87*2DI+r 1899 0 obj <>stream 0000004095 00000 n When the seller offers the pricing below market rates; When the seller claims that they can import iHealth tests directly from China. U The FDA has made tests available under an emergency access mechanism called an Emergency Use Authorization (EUA). "An extended expiration date means the manufacturer provided data showing that the shelf-life is longer than was known when the test was first authorized," the FDA says. Most of our tests may be available through your healthcare provider or at retail pharmacies. Abbott received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA) for the ID NOW COVID-19 test in March 2020. Antibody testing is an important step to tell if someone has been previously infected. This test has not been FDA cleared or approved. *sOi:o1_o7&}9t_bv4]S=dy*]?moi,T|*iwM1=)?uc>fX1gY%'xM^7 dNrNrdvdJ|ZZKOOZ;>&TnnNV&|zr9a_LaL}p,K/A_})nJ7MtS)nJG+jH7\bL:b:L}0 EQ The website that you have requested also may not be optimized for your screen size. pR N_q :l@\/9`ho}.M^:nYu_x);|!WCyP#$U1M6 qht 'hR00U8s5Bc9U+R+XhFo.AZB`08'tH If you're with a hospital, lab, or healthcare provider, you can contact us for questions about ID NOW here. x]>q"%>Ip]=i>lMn'l2I,nfgMKIS|(|_^}_Cg=~WW/^{xx/^|W=5m_~r3{2trS~S[7{iOo5OWo?O4j-te/m.Ue6~w|7~y~8]Mo^s?_;95qf{aKqrKx-yc|.?]nK{F;knC{a5OUH{` So here's how to know if your at-home test kits are still. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The Philadelphia Inquirer (TNS), Subscriber Verification(Must be Logged In Using Free Account). For more information on our ARCHITECT antibody test, check out this article: https://abbo.tt/3abd0eq This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. The expiration date printed on your at-home COVID-19 test kits may not be accurate. Invalid password or account does not exist. 0000003892 00000 n f$Rx98|)`DHC03)7ckzUV,|$^gwHt0j eY3@54Pdkn6M8D42Z3h5E1l}^PC7B17jnhC96sBA>TtCBMEYu^tHtZSze.qT}{V5}_^Ux. Sign up to receive news and updates from this site directly to your desktop. 0000004942 00000 n They are still fine, according to WHEC, the NBC affiliate in chilly Rochester, New York, which posed that question to manufacturers. %%EOF Q4{y4(L7M&e~XzhkHAj!USV{{eE =BXoZ(BMr2d+)2rElxJE:t_h_Y9e*r yP/t !N HOW LONG HAS THE ID NOW INSTRUMENT BEEN IN USE? It can be used in three different ways. Read more about ARCHITECT: https://abbo.tt/3abd0eq Press the space key then arrow keys to make a selection. If coronavirus proteins are present in the sample, the antibodies bind to them in such a way that the strip changes color, said Volk, chief medical officer of Baptist Health Floyd Hospital in New Albany, Indiana. For more information on m2000, check out this article: https://abbo.tt/2U1WMiU, We also have a molecular test for our Alinity m system under the FDA's Emergency Use Authorization. HVMo8W(CR(E&i]4E This allows for fast test results since they dont need to be sent out. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. H\j@}l/4 `t The FDA advises against using at-home Covid tests past their expiration date, because tests and their parts can break down over time. 0000001933 00000 n h`=@^2/W2Q\% [2x?}N8BCExT'+N Frs&41MU]/Rz{{\,O)JEgm1//Q{Z0\ve!'b@1I9\&jp,*\VALtPAew;$9gD"D-ubEn_"me*we@!jV!8&+t .}S-Fv\EZ%!ko5*axvKfsuQxU2ZM-~Z`{-Gm%ryA,=-hh5{`:*o:pcv{7MYvO%UY7yZM>q?J*QYO\tTgzO 5$~`1. Winds light and variable.. A clear sky. Testing has been completed to support a shelf-life (expiration date) of up to 15 months. !}TO'Y7@O/+Ol&i5`W]bq0!nA^C>VKjMp:J}C a:!F 3130 0 obj <>stream 109 0 obj <> endobj o Abbott Panbio COVID -19 AG Rapid Test Device (nasal) (December 31, 2020) . Learn more about ARCHITECT here: https://abbo.tt/3abd0eq, Learn more about Alinity i here: https://abbo.tt/2SWCvtU. 0000020161 00000 n Abbott is providing these links to you only as a convenience, and the inclusion of any link does not imply endorsement of the linked site by Abbott. 869 0 obj <>stream They have a shelf life. An email message containing instructions on how to reset your password has been sent to the e-mail address listed on your account. Cqv1Xpl%3,QC~:?[>27C 8Bc u6{Wn7:gZk"W8'4 xdtN=$cM0.zuFTu%@"($O~p_7MeLq'{(0KdkJ1PQ? It will provide a better understanding of the virus, including how long antibodies stay in the body. The website you have requested also may not be optimized for your specific screen size. endstream endobj 162 0 obj <>stream Expiration details by test type: ABBOTT BinaxNOW: The FDA has approved an amended EUA for Abbott BinaxNOW antigen tests, extending the effective shelf-life. 0000005785 00000 n The agency announced that Abbott's BinaxNow COVID-19 Ag Card Home Test is now approved for a 15-month expiration window. Even Abbott, which has years of experience making similar tests for other purposes, has extended the expiration dates on its COVID tests several times, after demonstrating that the components remain stable. We continue to work closely with our customers around the world to bring testing to where its needed most. 0000001341 00000 n No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. The direct swab method is the best way to ensure the test performs as expected. endstream endobj 161 0 obj <>stream startxref The chemistry behind the antigen tests typically depends on two key components: a liquid reagent that is used to extract protein fragments from the patient sample, and customized antibodies that are painted on the test strip. Biolabs International LLC / GriffMaier LLC, Paramount Sourcing LLC (exclusively partnered with Office Depot), Sunshine Paper LLC / Marketing Promotion Image Inc. Many of these instruments are already located in hospital and academic medical center labs where patients go for care. Molecular testing: Take a look at this infographic on how coronavirus molecular testing works. Since the U.S. Centers for Disease Control and Prevention began allowing inbound travelers to fly into the United States with a negative result from an at-home instant COVID-19 test in May, just two tests have been approved for use Abbott's BinaxNow COVID-19 Home Test and Ellume's COVID-19 Home Test.. On Oct. 1, Ellume voluntarily recalled more than 2 million tests, citing "higher-than . 0000015920 00000 n For a crash course on what is meant by expiration in this context, and how to make sure your test is still OK, we spoke to Emily Volk, president of the College of American Pathologists, and Matthew Pettengill, director of clinical microbiology at Thomas Jefferson University Hospital. Rapid antigen tests offer several important benefits. %%EOF But stick to the recommended temperatures as much as possible. !}TO'Y7@O/+Ol&i5`W]bq0!nA^C>VKjMp:J}C a:!F 0000008006 00000 n Abbott has been a global leader in infectious disease testing for decades, having developed the world's first HIV test. endstream endobj 849 0 obj <. {]Tuvpnl/'|PZge~MDlegn{O:>'S9kDI#LqGTj?#]aT?!8y+vX4[{cWLh7qqrR_~ibzcDjbkU 159 0 obj <>stream HOW LONG DOES IT TAKE TO GET RESULTS FOR THE ID NOW TEST? ID NOW is a lightweight and portable instrument (just 6.6 pounds and the size of a toaster) that allows testing to occur near the patient to get rapid results including in physicians' offices, urgent care settings, and hospital emergency departments. 848 0 obj <> endobj 0000003440 00000 n %%EOF Serology testing: For more information on how testing for antibodies works, check out this infographic. Were continuing to ramp up our ID NOW manufacturing and plan to increase capacity to 2 million tests a month by June and are working to expand beyond that. hbbbf`b``30 An extended expiration date means the manufacturer provided. Our rapid, molecular point-of-care test detects COVID-19 in 13 minutes or less. Winds light and variable. For general questions about BinaxNOW COVID-19 Ag Card: https://abbo.tt/2Qk76jp, For general questions about ID NOW: https://abbo.tt/2P8bYru, For general questions about m2000: https://abbo.tt/3fcjz2P, For general questions about ARCHITECT: https://abbo.tt/2X4m9RZ, For general questions about Alinity i: https://abbo.tt/335jaN6, For general questions about Alinity m: https://abbo.tt/2X754XS. These tests have been authorized by FDA under EUAs for use by authorized laboratories and have been authorized only for the detection of nucleic acid from SARS-CoV-2 or detection of IgG antibodies against SARS-CoV-2, and not for any other viruses or pathogens. Learn more about m2000 here: https://abbo.tt/3b8bASF, Alinity m systems have the ability to run high volumes of up to 1,080 tests in 24 hours, helping to meet the increasing demand for testing. 0000166958 00000 n :C1lr"wiUog-+Wu4W_*_EVqX~/,Lgj>Am=1-ij [)l+vr}H\b5&k?~s?YJgX?9n/t(8,?zzIc^|vxH>_{$HH>X{F)"y$sDmA=Jd:"'Vvu;;iX[g More than 800,000 rapid COVID-19 tests passed their expiration date recently in a Florida warehouse, prompting concerns that they would go to waste. Since the start of the pandemic, Abbott has produced and shipped more than 2 billion COVID-19 tests. 0000009168 00000 n endstream endobj 160 0 obj <>stream 0 Most of these antigen tests have a pretty good shelf life, he said. Currently, the ID NOW COVID-19 test is available only in the U.S. under emergency use authorization (EUA) as this is where the majority of our ID NOW instruments are in use today. For more information on our IgM antibody test, check out this news release: https://abbott.mediaroom.com/2020-10-12-Abbott-Receives-FDA-Emergency-Use-Authorization-for-its-COVID-19-IgM-Antibody-Blood-Test. The expiration dates of the lot numbers listed in the referenced link have been extended to 12 months. ID NOW is an FDA approved CLIA-waived instrument, which means that the technology can be used in settings outside the traditional hospital setting. Charles Passy President Biden is ending the country's COVID emergency declaration, which means Americans may no longer get free tests. $E;n7$%YJ{^,Y7ofx->XB7oOOB+.N#EIE(.2t-Vgcv)~&(f;#X{L21R+Mk.U eM,+D]q/K&KwDA6=WWOBNP|:SX!\GUEaaw)eJQBS8o9;[&}EZ$,,58@7$2v AU$pRB8SYzt)^S 2*g5 No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Low 33F. Abbott and the regulatory approval of Panbio Covid-19 Version NP test Abbott is an American company that holds 365 medical device licenses in Canada under 19 . BinaxNOW COVID-19 Self Tests are available at major U.S. food, drug and mass merchandiser retailers across the country. In the case of Abbotts BinaxNOW tests, the date is printed alongside a small icon of an hourglass. The systems have the ability to run high volumes of up to 470 tests in 24 hours, helping to meet the increasing demand for testing. Our first molecular test is used on our lab-based molecular instrument, m2000. Theyre pretty stable for over a year.. But for certain tests, that expiration date may have been extended beyond what is stamped on the package provided the manufacturer has demonstrated to the FDA that the components remain stable. With the number of cases still high, youll likely be using the test long before that date anyway. ID NOW has been in use since 2014 to detect flu, strep, and RSV. Learn more. The first-of-its-kind app, available at no charge, allows people who test negative to get a temporary digital health pass that's renewed each time the person has a negative test. 0000015990 00000 n In some cases, the expiration date for a test may be extended. HOW WERE YOU ABLE TO DEVELOP TESTS SO QUICKLY? The expiration date to reference is the one on the outside of the box by the hourglass icon. WILL YOUR RAPID TESTS BE AVAILABLE IN DRIVE-THRUS OR FOR AT-HOME USE? 0000166652 00000 n 0000038489 00000 n o In some cases, the companies have inserted notices into the packages with the updated info. 0000002295 00000 n agr. Organizations like employers and schools have the option to use the app to view and verify the information on a mobile device to facilitate safer entry into facilities along with hand-washing, social distancing, enhanced cleaning and mask-wearing. Click on the bell icon to manage your notifications at any time. Get up-to-the-minute news sent straight to your device. For more information on the Alinityi system, check out this news release: https://abbo.tt/2SWCvtU The type of Abbott tests in the Florida warehouse are now deemed to have a shelf life of 15 months, up from 12. Testing has been completed to support a shelf-life (expiration date) of up to 15 months. Generally, the expiration dates are stamped on the back of the package. You have permission to edit this article. These tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. 0000166391 00000 n The ID NOW testing process is safe and does not endanger operators as long as the collection and processing of samples follow the universal precaution techniques outlined by CDC guidelines. The test does not need any . In others, new expiration dates are posted on company websites, organized by lot number, but finding them can be a challenge. Read more about Alinity i: https://abbo.tt/2SWCvtU 2021, Health Canada authorized an amendment for a shelf life extension from 12 to 24 months. Our ID NOW molecular point-of-care test met all testing criteria in the FDA's emergency use authorization (EUA) and were continuing to collect more clinical data in the field. For our rapid antigen tests, BinaxNOW is available in the U.S. and Panbio is available in many countries outside of the U.S. For more information on ID NOW check out this article: https://abbo.tt/2UT36cN. 0000151822 00000 n 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. 0000105378 00000 n Learn more about Alinity m here: https://abbo.tt/2zrt52N, ID NOW delivers positive results in as little as 5 minutes and negative results in 13 minutes. XsVxIRvD/-QUdv}S j%/=C5uT#L7hfGnBJwD| D=X\P+/lSD-cXCiT!GwPg0+kmBrh>Che|V4!cXuoHKeKk7lKr/XCLg+VEoGi' R~H}2-yLiQi59\9,bWKBSAP_orkW8h`f$C\*6eM! WHAT'S THE TURN-AROUND TIME FOR YOUR TESTS? 0000002907 00000 n A single at-home COVID-19 test by Quidel sits on a drugstore shelf on Sept. 14, 2021, in Chicago. Our rapid antigen test, BinaxNOW COVID-19 Ag Card, Home Test and Self Test all provide results in 15 minutes. Please be aware that the website you have requested is intended for the residents of a particular country or region, as noted on that site. To be on the safe side, use a test that has not expired. If you're with a hospital, lab or healthcare provider, please see the contact details below. trailer Posted on 11/05/2021 You can access the most information related to Abbott of BinaxNOW tests that have been authorized to have their expiration dates extended by accessing information directly from Abbott's website. Here's how to tell, By Tom Avril We have molecular and antigen tests that help detect an active infection of COVID-19, as well as serology tests that help detect antibodies. <<6E9C363DB97F0F4FA676E3E40C7FF57B>]/Prev 190041/XRefStm 1630>> U %PDF-1.4 % endstream endobj 121 0 obj <> endobj 122 0 obj <>stream 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. pR N_q :l@\/9`ho}.M^:nYu_x);|!WCyP#$U1M6 qht 'hR00U8s5Bc9U+R+XhFo.AZB`08'tH 0000012590 00000 n HOW ACCURATE ARE THE ID NOW COVID-19 TESTS? kdv1_2x/ This test has been authorized by FDA under an EUA for use by authorized laboratories. H\n@E^& %PDF-1.6 % Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. Hs"`S*2rT0 T$ T h`=@^2/W2Q\% [2x?}N8BCExT'+N Frs&41MU]/Rz{{\,O)JEgm1//Q{Z0\ve!'b@1I9\&jp,*\VALtPAew;$9gD"D-ubEn_"me*we@!jV!8&+t .}S-Fv\EZ%!ko5*axvKfsuQxU2ZM-~Z`{-Gm%ryA,=-hh5{`:*o:pcv{7MYvO%UY7yZM>q?J*QYO\tTgzO 5$~`1. D iHealth Rapid . 0000002428 00000 n Has your COVID rapid test expired? f$Rx98|)`DHC03)7ckzUV,|$^gwHt0j eY3@54Pdkn6M8D42Z3h5E1l}^PC7B17jnhC96sBA>TtCBMEYu^tHtZSze.qT}{V5}_^Ux. 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. Testing has been completed to support a shelf-life (expiration date) of up to 9 months from Date of Manufacture. More than 800,000 rapid COVID-19 tests passed their expiration date recently in a Florida warehouse, prompting concerns that they would go to waste. Expiration details by test type: ABBOTT BinaxNOW: The FDA has approved an amended EUA for Abbott BinaxNOW antigen tests, extending the effective shelf-life. But the exact date in each case is an open question, in part because some of the manufacturers are new at this game. endstream endobj startxref ,2NuXua+2kq'jM&e:MO_>{%yw4g{9vp:am+#E?&F%*(h[iE+[x~_]N2IZNr-]N^^v)j$QN/7_8#9tE'nrM^M'N3u~*vaBgb2)zU{ eu endstream endobj 158 0 obj <>/Filter/FlateDecode/Index[8 101]/Length 24/Size 109/Type/XRef/W[1 1 1]>>stream But the manufacturer, Abbott, obtained. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions. If you are an individual, please reach out to your healthcare provider. CHECK OUT THESE HELPFUL LINKS. hlj@E.3AF,lKS(a2/IuwsOC"A"(H>C)DBsHshJbmBLX+XpEOr We won't share it with anyone else. Abbott says its tests can be stored between 36 to 86 degrees Fahrenheit, but that the kits should be at room temperature at the time they are used. Our rapid antigen test,BinaxNOWCOVID-19 Ag Card, Home Test and Self Test allprovide results in 15 minutes. "Ds>f`bdd100"M` This letter is to notify you the BinaxNOW COVID-19 Ag Card, part number 195- Please be cautious of the following situations: Below is a list of iHealths authorized distributors (in alphabetical order): If you want to verify whether a seller not on the list is authorized to distribute iHealth tests, please contact us at legal@ihealthlabs.com. %PDF-1.6 % Use left/right arrows to navigate the slideshow or swipe left/right if using a mobile device, OnJan 11, 2023, the FDA granted another three-month shelf-life extension for the iHealth COVID-19 Antigen Rapid Test, which extended the shelf-life of all iHealth testsf. We will continue to apply to FDA for shelf-life extensions every three months based on our stability studies, and the new shelf-lives for our tests will apply to tests already produced as well as future production.