Direct Load Tube Collection Kit*

Transform specimen processing for COVID testing

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

 

One-Step Workflow — Deliver Results Sooner

 

Traditional Respiratory Specimen Workflow

 

Reduce Labor, Costs and Risk with Fewer Steps

     

 Eliminate manual uncapping and recapping

 

 One collection kit for nasal and OP swabs

     

 Remove manual specimen transfer steps

 

 Inactivates common respiratory viruses

     

 Reduce human error and repetitive motion injuries

 

 Guanidine free, non-toxic media

     
 Reduce costs for additional consumables    Penetrable cap serves as additional cross-contamination barrier

 


* 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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