Explore Brevera Breast Biopsy System

Explore Brevera Breast Biopsy System

360° View

Intuitive Interface

Real-Time Core Imaging

Dedicated Technologist Screen

Flexible Dual Monitors

Improved Core Handling

Streamlined Design

Explore the Device

Remote Operation

a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).
Explore Brevera Breast Biopsy System

Dedicated Technologist Screen

Select one of the modality buttons to see more.

a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Remote Operation

Remote operation for biopsy, lavage, aspirate, and standby frees technologists to focus on patients while giving physicians full control of the procedure.

a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Improved Core Handling

The collection and post-biopsy preparation of tissue samples is streamlined and requires little to no manual handling.

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a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Real-Time Core Imaging

See the Brevera system’s real-time imaging in action.

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a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Intuitive Interface

Designed with physicians in mind and relevant, easy to use features. Quickly verify samples with a comprehensive suite of imaging tools, and access patient worklist to help streamline workflow.

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a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Flexible Dual Monitors

With swivel, rotation, tilting and adjustable heights, the system monitors provide the customizable configurations to suit any user preferences.

a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Streamlined Design

The Brevera system is designed to minimize footprint and work seamlessly with imaging equipment in the biopsy suite.

a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

Vacuum assisted tissue acquisition

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a. Brevera Breast Biopsy System 510(k) Premarket Notification, K163052, U.S. Food and Drug Administration. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163052 (Accessed July 30, 2024).

360° View

Click and drag below to rotate the console for a 360° view.