Hologic Brevera Breast Biopsy System

Hologic Brevera Breast Biopsy System

Product Name:
Hologic Brevera Breast Biopsy System
Modality:
Biopsy
Manufacturer:
Hologic
System:
Brevera
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Product Details

Hologic Brevera Breast Biopsy System Overview

The Hologic Brevera breast biopsy system integrates real-time specimen imaging directly into the biopsy device through CorLumina imaging technology, eliminating the need to remove tissue samples for separate specimen radiography during the procedure. This transforms the traditional 8-step stereotactic biopsy workflow into a streamlined 3-step process, reducing average procedure time to approximately 12 minutes and providing real-time specimen verification without leaving the biopsy position.

CorLumina Imaging Technology

CorLumina is Hologic's proprietary real-time specimen imaging technology built into the Brevera system. As tissue samples are acquired by the vacuum-assisted biopsy needle, they are automatically collected, separated, and imaged within the Brevera handpiece and console. High-resolution specimen images appear on the touchscreen interface, allowing the radiologist to immediately verify that targeted calcifications or lesion tissue have been successfully sampled without interrupting the procedure.

Streamlined 3-Step Workflow

  • Step 1 - Target: The lesion is identified and targeted using the Affirm biopsy guidance system with stereotactic or tomosynthesis-guided targeting
  • Step 2 - Acquire: The vacuum-assisted biopsy needle acquires tissue samples, automatically collected and separated within the system
  • Step 3 - Verify: CorLumina provides real-time specimen images on the touchscreen for immediate verification that the targeted finding has been captured

Clinical Benefits

  • 25%+ reduction in procedure time: Average procedure time of approximately 12 minutes compared to conventional stereotactic biopsy workflows
  • Less patient compression time: Eliminating external specimen imaging steps reduces total time under breast compression
  • Improved diagnostic confidence: Real-time specimen verification confirms biopsy adequacy before concluding the procedure
  • Reduced need for post-biopsy specimen radiography: CorLumina provides specimen verification within the biopsy workflow
  • Intuitive touchscreen interface: Real-time specimen images, procedure status, and system controls in a single integrated display

System Integration and Compatibility

The Brevera integrates with Hologic Affirm biopsy guidance systems in both prone and upright configurations. It is compatible with Selenia Dimensions and 3Dimensions (Genius) mammography platforms equipped with Affirm, allowing facilities to add Brevera capability without replacing their primary imaging system. The console connects to the Affirm system for targeting coordination, and specimen images can be exported to PACS for documentation.

ARRAD Sales, Installation, and Service

ARRAD provides complete lifecycle support for the Brevera system, from purchasing through installation, training, and ongoing service. The system is available in new and professionally refurbished configurations. Our nationwide 24/7 service network keeps your Brevera operational with factory-trained engineers for preventive maintenance and repair. OEM parts and consumables are available through radmedparts.com.

Contact ARRAD at 877.299.8303, visit arrad.net/pages/contact-us to request a quote, or learn more at arrad.net/pages/hologic-service.

What is the Hologic Brevera breast biopsy system?

The Brevera is a vacuum-assisted breast biopsy system with integrated real-time specimen imaging powered by CorLumina technology. It combines tissue acquisition and specimen verification into a single device, streamlining the workflow from 8 steps to 3 steps with an average procedure time of approximately 12 minutes.

How does the Brevera 3-step workflow differ from a traditional biopsy?

A traditional stereotactic biopsy involves up to 8 steps including separate specimen transport and imaging on an external system. The Brevera consolidates this into 3 steps: target, acquire, and verify using real-time CorLumina imaging on the integrated touchscreen, all without leaving the biopsy position.

How long does a Brevera biopsy procedure take?

The average Brevera procedure takes approximately 12 minutes, a 25% or greater reduction compared to conventional stereotactic biopsy workflows. The time savings come from eliminating the need to pause for external specimen imaging.

Is the Brevera compatible with my existing Hologic mammography system?

The Brevera works with Hologic Affirm biopsy guidance systems in prone and upright configurations, integrating with Selenia Dimensions and 3Dimensions (Genius) platforms. Contact ARRAD at 877.299.8303 to verify compatibility with your specific configuration.

Does ARRAD provide service and support for the Brevera system?

Yes. ARRAD offers complete Brevera support including sales, installation, clinical training, preventive maintenance, and 24/7 nationwide repair service. OEM parts and consumables are available through arrad.net. Contact us at 877.299.8303.

FAQ

Frequently Asked Questions

What is the difference between Selenia Dimensions and 3Dimensions (Genius)?

Both platforms offer industry-leading 3D tomosynthesis with excellent dose efficiency. The Selenia Dimensions is a proven workhorse trusted by tens of thousands of facilities worldwide, while the 3Dimensions (Genius) platform is the newer flagship system with enhanced software features, faster acquisition speed, and improved workflow integration. Both are excellent choices; the selection depends on your facility's volume, budget, and preferences for newer technology versus field-tested reliability.

Can I upgrade an existing Hologic system to tomosynthesis?

Software tomosynthesis upgrades are typically available for qualifying systems, though hardware requirements and licensing vary. Older analog systems cannot be upgraded. We recommend contacting our team with your specific system model for an assessment—our engineers can evaluate upgrade feasibility and cost-effectiveness compared to purchasing a refurbished tomosynthesis unit.

What does MQSA compliance mean, and why does it matter?

MQSA (Mammography Quality Standards Act) compliance ensures that mammography equipment meets federal standards for image quality, dose management, and safety. All mammography systems sold in the United States must maintain MQSA certification. AR-RAD conducts physicist testing and calibration for every unit we sell to guarantee MQSA compliance and regulatory readiness for your facility.

How long does installation and training typically take?

Installation typically requires 1-3 days depending on site preparation status and room modifications needed. Technologist and radiologist training is usually 2-5 days. We coordinate the entire process with your staff and can often overlap installation with training to minimize downtime. Our factory-trained technicians handle all setup and calibration work.

What warranty and service options does AR-RAD offer?

We offer flexible warranty packages ranging from 90 days to 5 years, plus optional service contracts that cover parts, labor, and preventive maintenance. Since we're an authorized service provider with nationwide coverage, your facility benefits from local support through our Lake Forest, California headquarters with the ability to serve any location across the US, Canada, and Mexico.

Are refurbished Hologic systems as reliable as new ones?

Yes. Our refurbishment process is rigorous: every detector is tested against ACR phantom standards, all mechanical systems are recalibrated, and new high-wear components are replaced. Many of our refurbished systems perform identically to new equipment at 40-60% of the cost, making them an excellent value for facilities with stable budgets.

How do I know which detector my Hologic mammography system needs?

Each Hologic mammography platform uses a specific detector assembly. Original Selenia FFDM systems use the ASY-00834 (standard cycle) or ASY-01389 (fast cycle) detectors. Selenia Dimensions systems use the PRD-00779 or PRD-01702 HDT detector depending on the configuration. Hologic 3Dimensions (Genius) systems use the PRD-04420 Clarity HD detector. These detectors are not interchangeable between platforms. Contact ARRAD with your system serial number and we will confirm the exact detector part number your system requires.

What is ARRAD's detector exchange program?

Our detector exchange program ships a quality-assured replacement detector to your facility before you return the failed unit. This minimizes mammography suite downtime by allowing your service engineer to install the replacement panel as soon as it arrives. After installation, you return the original detector using our provided shipping materials. Exchange pricing is typically lower than outright purchase, making this an attractive option for facilities managing equipment budgets.

What causes mammography detector failure?

Mammography flat-panel detectors degrade over time through several mechanisms. The amorphous selenium layer gradually crystallizes, reducing its ability to convert X-rays to electrical signals. Individual transistor elements in the TFT readout array can fail, creating dead pixels. Thermal cycling from daily power-on and power-off stresses electronic connections. Signs of degradation include increasing dead pixel counts, calibration instability, declining ACR phantom scores, and visible image artifacts. Regular quality control testing helps identify degradation trends early so replacement can be planned before clinical image quality is affected.