1. Simplified Workflow
1. Simplified Workflow
2. Market-Leading Diagnostic Tests
2. Market-Leading Diagnostic Tests
Hologic's collection devices support a comprehensive testing portfolio for women's health and infectious disease, including SARS-CoV-2, that has been rigorously developed for highly accurate and reliable results.
3. Scalable Automation
3. Scalable Automation
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.
Collection Devices
Reference
Collection Devices
Reference
Assay Menu
CT/NG
Mycoplasma genitalium
Trichomonas vaginalis
Bacterial vaginosis
Candida vaginitis/Trichomonas vaginalis
HSV 1 & 2
Aptima® Multitest Swab Specimen Collection Kit
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.
Direct Load Tube Specimen Collection Kit
The Direct Load Tube Collection Kit is intended to be used for collection of the following swab specimen types: Nasal and oropharyngeal.
Aptima® Unisex Swab Specimen Collection Kit
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.
Zika Virus†Aptima® Urine Specimen Collection Kit
The Aptima Urine Specimen Collection Kit is intended to be used for the collection and transport of male or female urine specimens.
Assay Menu
SARS-CoV-2*
Direct Load Capture Cap Collection Kit
The Direct Load Capture Cap Collection Kit is intended to be used for collection of the following swab specimen types: Nasopharyngeal (NP) swabs.
Transfer Tubes
Reference
Transfer Tubes
Reference
Assay Menu
CT/NG
Mycoplasma genitalium
Trichomonas vaginalis
HSV 1 & 2
HPV
HPV 16 18/45
Group B Strep
Aptima® Specimen Transfer Kit
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.‡
Panther Fusion® Specimen Lysis Tube
Specimen Lysis Tubes and Specimen Transport Medium (STM) are intended to be used for processing specimens for use with Hologic assays.‡
Aptima® Specimen Aliquot Tube
Aptima Specimen Aliquot Tubes (SAT) are intended for use with plasma and serum specimens that will be tested with Aptima® quantitative assays. SATs are included in the Aptima® Specimen Diluent Kit.‡
Streamline your workflow from patient collection to results
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*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.
*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.
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