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ID NOW TM COVID-19 <br />�,r e U <br />h ktfle as �)rt e s <br />S 1) E E I) e <br />nl?st dts �'r) ("),i'4 I, Lrt e s,,' <br />5-13 <br />Timely results enable healthcare professionals to make MINS <br />appropriate and more efficient treatment and infection <br />control decisions. <br />ID NOW" COVID-19 <br />�Ir E C H �I"',411 0 1. 0 G Y <br />�)o ocess <br />( .... . ... ...... <br />V <br />0" <br />)l ..... . ..... ...... <br />ORDER INFORMATION <br />in a variety of environments" <br />PRODUCTNAME <br />• Assay kit contains all necessary components <br />IDNOW-COVID-19 <br />24 TEST <br />Izes l l <br />0 U� r", <br />�E di� I dlogy <br />CONTROL KIT <br />a �r'ii l I '�f[, U, <br />lv e <br />�f�' r, p r ov 'd r e <br />CPT <br />Cod e: 8 7 635 <br />- Positive and negative control swabs <br />• Room -temperature storage <br />g <br />�t­ r �1� <br />C I.,� �1 a r l S <br />t S <br />I tl e <br />�if r a r [(,, <br />e i,,:' <br />EASE OF USE , & r�I p i, �,,e 'test <br />�)o ocess <br />• Designed for near -patient testing <br />ORDER INFORMATION <br />in a variety of environments" <br />PRODUCTNAME <br />• Assay kit contains all necessary components <br />IDNOW-COVID-19 <br />24 TEST <br />for testing, including: <br />KIT <br />111. 1 . DNOW - COVID-19 <br />- 24 tests <br />CONTROL KIT <br />- Swabs for sample collection <br />(12 POSITIVE, 12 NEGATIVE) <br />I 11 I - - .- - <br />- Pipettes <br />CPT <br />Cod e: 8 7 635 <br />- Positive and negative control swabs <br />• Room -temperature storage <br />eliminates need for refrigeration <br />PRODUCTCODE <br />110�1# I I <br />190-080 <br />(C) M 0 U U E 0 N F0, M AT <br />C N I" AC 1I" YO I,11 R U 0 C M A 1�1311, IB 0 TT 1 Z IE jj <br />S U,, ii TA V II,""' 0 F'Z, <br />V II S I A B U 4 u,'C,'1%, C 0 1,,Vi 0 CII <br />The ID NOW''"' <br />COVID-19 EUA has not been FDA cleared or approved. it has been authorized by the FDA under an emergency use <br />authorization for use by authorized laboratories and patient care settings. The test has been authorized only for the detection Of <br />nucleic acid frorn SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that <br />circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of <br />COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. 9 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. <br />11D NOW''"' <br />COVID-1.9 detects positive results in as a little as 5 minutes, Negative results detected in 13 minutes. <br />**Please see ID NOW Instrument user manual for additional operating environment requirements. <br />1. Internal clinical data held on file. <br />CG 2020 Abbott. All rights reserved. All trademarks referenced are trademarks of either the Abbott group of Ell, <br />companies or their respective owners. Any photos displayed are for illustrative purposes only: <br />120006407-0103/20 Abbott <br />