Consolidate testing with direct load collection devices.
With a simplified workflow, market-leading diagnostic tests and scalable automation, you can trust Hologic as your long term testing partner.
Deliver Results Sooner
Load directly into the Panther® System
Directly load alongside specimen types for other assays with true random and continuous access.
Non-hazardous lysis buffer reduces risk by inactivating common respiratory viruses, minimizing biosafety needs.
Penetrable cap creates additional cross contamination barrier and eliminates uncapping and recapping of tube.
Market Leading Diagnostic Tests
Hologic's collection devices support a comprehensive testing portfolio for women's health and infectious disease that has been rigorously developed for highly accurate and reliable results.
Panther Scalable Solutions allows you to expand your testing menu while increasing flexibility, capacity and walkaway time. Load samples with Hologic’s collection devices or transfer tubes at any time with true random and continuous access, expediting turnaround time.
The Aptima Multitest Swab Specimen Collection Kit is intended to be used for collection of the following swab specimen types: vaginal, rectal, throat, penile meatal, nasal and anogenital lesions. Learn More.
The Aptima Unisex Swab Specimen Collection Kit is used for the collection of female endocervical or male urethral swab specimens. It is also intended for use in sampling other previously collected specimens for processing, extraction, and analysis with other Hologic products.
The Aptima Specimen Transfer Kit is intended for use with Aptima assays for the testing of gynecological specimens collected in ThinPrep® Pap Test vials containing PreservCyt® solution. It is also intended for use with other Aptima assays and other Hologic products.‡
*The Aptima® and Panther Fusion® SARS-CoV-2 assays: These tests have not been FDA cleared or approved; These tests have been authorized by FDA under an EUA for use by authorized laboratories; These tests have been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens; and 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. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
†The Aptima Zika Virus 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 RNA from Zika virus and diagnosis of Zika virus infection, 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 the emergency use of in vitro diagnostic tests for detection of Zika virus and/or diagnosis of Zika virus infection under section 564(b)(1) of the Act, 21 U.S.C.§ 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
‡Refer to the appropriate product package insert for the indicated uses of the transfer tubes for each Hologic product.