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Quidel has developed an innovative line of respiratory products for decades.


So whatever respiratory season may bring, we’re ready.


1979 founded Quidel


Receives FDA


1999 y Õiâ> /iÃÌ ­ƂÉ ® y Õ ÌiÃÌ +ÕV6Õi


clearance for world’s w ÀÃÌ À>«` `>}ÃÌV


2015 Solana assays Introduction of


,iViÛià -Ƃ,- ƂÌ}i 2020 -Ƃ,- 6Ó


Ƃ 1Ƃ vÀ -w > Ó Ƃ] -w > Ó Õ³


SARS FIA (ABC), QuickVue SARS Antigen Test, and Solana


2011 automated analyzer FIA +Õ`i >ÕVià -w >


First company to receive


1996 +ÕV6Õi  i -ÌÀi« Ƃ /iÃÌ CLIA waiver for Strep A with


2018 which meets FDA’s Class II +ÕV6Õi y Õiâ> Ƃ³


RIDT requirements Receives FDA clearance for


QuickVue® y Õiâ> Ƃ³ ] ,-6] SARS* Antigen Assays


Solana® y Õiâ> Ƃ³ ] ,-6 ³  *6] -Ƃ,- 6ÓI]


À`iÌi> Complete Assays To get the right RIDT for your patient, contact a Quidel Inside Sales at 858.431.5814 or visit quidel.com


*THESE TESTS ARE AVAILABLE FOR SALE IN THE USA UNDER EMERGENCY USE AUTHORIZATION. These SARS tests have not been FDA cleared or approved, but have been authorized LÞ Ìi Ƃ Õ`iÀ > iÀ}iVÞ 1Ãi ƂÕÌÀâ>Ì ­ 1Ƃ® vÀ ÕÃi LÞ >ÕÌÀâi` >LÀ>ÌÀià vÀ Ìi `iÌiVÌ v «ÀÌià ­+ÕV6Õi >` -w >® À ÕViV >V`à ­->>® vÀ -Ƃ,- 6Ó] Ì for any other viruses or pathogens. These tests are only authorized for the duration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection >`ÉÀ `>}Ãà v "6 £ Õ`iÀ -iVÌ xÈ{­L®­£® v Ìi i`iÀ> `] ÀÕ} >` ÃiÌV ƂVÌ] Ó£ 1°-° ° Å ÎÈäLLLέL®­£®] ÕiÃà ÌiÀ>Ìi` À ÀiÛi` ÃiÀ°


Ƃ £ä£nÎÈää ää ­äÈÉÓÓ®


5QƂ C®


5QƂ C


y Õiâ> Ƃ³ ] ,-6] -Ƃ,-I Antigen, Õ ³ -Ƃ,-I ƂÌ}i ƂÃÃ>ÞÃ


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