Direct Load Capture Cap Collection Kit*

Transform specimen processing for COVID testing

No specimen transfer. Expedite your SARS-CoV-2† workflow with a collection device that loads directly on the Panther® system.


Two-Step Workflow — Deliver Results Sooner


Traditional Respiratory Specimen Workflow


Reduce Labor, Costs and Risk with Fewer Steps


 Eliminate manual specimen transfer steps


 One collection kit for nasal and OP swabs


 Reduce potential for human error


 Inactivates common respiratory viruses


 Remove costs for additional consumables


 Guanidine free, non-toxic media


* In development and not for sale.
† The Aptima® SARS-CoV-2 assay: This test has not been FDA cleared or approved; This test has been authorized by FDA under an EUA for use by authorized laboratories; This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens; and 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. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner,


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