NEW

FDA Releases Two Companion Reports on Medical Device Safety and Innovation

Today, the U.S. Food and Drug Administration’s (FDA) Center for Devices and Radiological Health Center (CDRH) is releasing two reports on medical device safety and innovation – the core pillars that help protect and promote public health for all. The “CDRH 2024 Safety...

Tri-Imaging, RTI Group Work Together

In a LinkedIn post, Tri-Imaging states, “We are honored to be the first ISO in North America to have the opportunity to try RTI’s new Mako X-Ray Testing Meter. The Mako meter is the most accurate and efficient testing meter that covers the broadest application range...

Detection Technology announces global availability of TFT flat panel detectors

Detection Technology, a global leader in X-ray detector solutions, announces the global availability of a comprehensive range of TFT (thin-film transistor) flat panel detectors. The portfolio includes IGZO (indium gallium zinc oxide) and a-Si (amorphous silicon)...

Bayer, Google Cloud Accelerate Development of AI-Powered Applications for Imaging

Bayer and Google Cloud have announced a collaboration on the development of artificial intelligence (AI) solutions to support radiologists and ultimately better serve patients. As part of the collaboration, Bayer will further develop its innovation platform to...

Hologic Updates Brevera Breast Biopsy System with CorLumina Imaging Technology

Hologic Inc. has announced improvements to the Brevera® Breast Biopsy System with CorLumina® Imaging Technology, the world’s first and only breast biopsy solution to combine vacuum-assisted tissue acquisition, real-time imaging verification and advanced post-biopsy handling in one, integrated system.

Since its launch in 2017, the Brevera system has shifted the way clinicians perform breast biopsies and verify that the targeted tissue samples have been acquired. The system streamlines the entire biopsy process from start to finish – with real-time imaging for verification of sample acquisition and automated post-biopsy specimen handling. These integrated features offer the potential to save facilities an average of 13 minutes per procedure to transform the patient experience and enhance workflow. In addition, they allow clinicians to remain by the patient’s side during the entire procedure, eliminating the need to leave the room to image and verify tissue samples, which often leads to lengthy procedure times and anxious patients, as well as interruptions to facility screening schedules.

“As a world leader in breast health, we take great pride in our commitment to constant innovation – informed by clinical research and customer feedback – to continuously expand and improve upon the performance of our products,” said Jennifer Meade, Hologic’s Division President, Breast and Skeletal Health Solutions. “The launch of the Brevera system represented a major transformation in breast biopsy, and we’re confident that the improvements we’ve introduced will further the system’s ability to enhance workflow, increase accuracy and improve the overall patient experience.”

To better meet clinician needs, the Brevera system features a reusable device driver and disposable needles to simplify storage and improve waste management. The system also features improvements that allow radiologists and technologists to better separate and verify target samples automatically, then transfer seamlessly to pathology with minimal handling to help maintain core integrity.

The Brevera system is designed for use with Hologic’s Affirm Prone biopsy guidance system. When paired together, the Brevera system and Affirm system accelerate the speed and efficiency of prone biopsy procedures to further reduce the patient’s time under compression.

Previous

Next

Submit a Comment

Your email address will not be published. Required fields are marked *

Open