MARLBOROUGH, Mass., Aug. 31, 2017 /PRNewswire/ -- Hologic, Inc.
(Nasdaq: HOLX) today announced U.S. commercial availability of the Brevera® breast biopsy system with
CorLumina® imaging technology, a groundbreaking real-time breast biopsy and verification system that enhances
workflow, improves the patient experience and streamlines the entire biopsy process from start to finish. The first-of-its-kind
Brevera system is designed to increase biopsy accuracy with real-time imaging that delivers valuable information at the point of
care, enabling clinicians to make informed decisions with confidence.
The Brevera system is the world's first and only breast biopsy solution to combine tissue acquisition, real-time imaging,
sample verification and advanced post-biopsy handling in one, integrated system. Designed for 2D and 3D™ breast
biopsy, the innovative system allows physicians to perform fast and efficient procedures that save costs and improve the patient
experience.1 The new product represents another major advance in Hologic's ongoing efforts to improve patient
satisfaction and workflow in the biopsy suite.
Until now, radiologists performing stereotactic breast biopsy procedures to diagnose breast cancer were often required to
leave the patient under compression while they moved to another room to image and verify tissue samples. This leads to lengthy
procedure times and anxious, uncomfortable patients, and can interrupt facility screening schedules. With the Brevera system,
radiologists are able to obtain and image tissue samples in the procedure room in just a few seconds, potentially saving up to 10
minutes per patient and cutting the procedure time by up to 25 percent.2
"We're proud to launch the Brevera system, a major breakthrough for radiologists who, for the first time, will be able to
image and verify tissue samples in real-time in the procedure room," said Pete Valenti, Hologic's
Division President, Breast and Skeletal Health Solutions. "The Brevera system provides clinicians with more information at the
point of care and women with a vastly improved experience, resulting in significant cost and time savings without compromising
accuracy or patient health outcomes. The system transforms the stereotactic breast biopsy procedure as we know it, and serves as
further proof of Hologic's commitment to better serve the needs of our customers and their patients."
In addition to saving facility resources and physician time during a breast biopsy procedure, the Brevera system's proprietary
CorLumina imaging technology helps enhance workflow across multiple departments within a health system. The CorLumina imaging
system automates the tissue sample collection and separation process, which allows patient tissue to be sent to pathology with
little or no manual handling and protects the integrity of samples. The system also features PACS integration for advanced image
sharing and transfer of patient records.
The Brevera system is designed for use with Hologic's Affirm® prone biopsy system, Affirm® breast biopsy guidance system, and
MultiCare® Platinum system, as well as most upright and prone systems on the market. For more information please
visit: www.BreveraBiopsy.com
About Hologic, Inc.
Hologic, Inc. is an innovative medical technology company primarily focused on improving women's health and well-being through
early detection and treatment. For more information on Hologic, visit www.hologic.com.
Hologic, 3D, Affirm, Brevera, CorLumina, MultiCare, The Science of Sure, and associated logos are trademarks and/or registered
trademarks of Hologic, Inc. and/or its subsidiaries in the United States and/or other
countries.
Forward-Looking Statements
This news release may contain forward-looking information that involves risks and uncertainties, including statements about
the use of Hologic products. There can be no assurance these products will achieve the benefits described herein or that such
benefits will be replicated in any particular manner with respect to an individual patient, as the actual effect of the use of
the products can only be determined on a case-by-case basis. In addition, there can be no assurance that these products will be
commercially successful or achieve any expected level of sales. Hologic expressly disclaims any obligation or undertaking to
release publicly any updates or revisions to any such statements presented herein to reflect any change in expectations or any
change in events, conditions or circumstances on which any such data or statements are based.
This information is not intended as a product solicitation or promotion where such activities are prohibited. For specific
information on what products are available for sale in a particular country, please contact a local Hologic sales representative
or write to womenshealth@hologic.com.
Media Contact:
Jane Mazur
508.263.8764 (direct)
585.355.5978 (mobile)
jane.mazur@hologic.com
Investor Contact:
Michael Watts
858.410.8588
michael.watts@hologic.com
1 3D biopsy only when used with the Affirm breast biopsy system.
2 2015 Kadence International survey of 200 healthcare professionals.
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SOURCE Hologic, Inc.