PickSuck and TissueCutSure Breast Biopsy System

PickSuck and TissueCutSure form a vacuum-assisted breast biopsy consumable system for ultrasound- or other imaging-guided tissue acquisition. The workflow is designed for hospitals and day-surgery settings that need reliable specimen volume, controlled retrieval, and pathology-friendly cores.

Clinical role

Breast lesion management often requires histology or cytology after imaging characterization. Minimally invasive vacuum-assisted biopsy (VAB) can reduce open surgical biopsies when guidelines support percutaneous sampling under imaging guidance. Disposable needle sets and tubing are intended for single-patient use to support infection control and traceability.

Indications (subject to IFU and local practice)

• Tissue sampling of breast lesions under imaging guidance (typically ultrasound; confirm compatibility with your imaging platform).
• Minimally invasive diagnostic pathways in hospital or ambulatory surgical programs.
• Programs that require consistent specimen handling for pathology review.

Core advantages

• Vacuum-assisted retrieval - supports stable specimen capture compared with purely manual cutting approaches in suitable lesions.
• Minimally invasive access - small skin entry; recovery expectations align with percutaneous breast procedures.
• Pathology-oriented workflow - cores sized and handled to support histologic assessment when protocol is followed.

Typical configuration

• Compatibility-oriented console / pump interface package (per regional registration).
• Single-use needle options in sizes cleared for your market.
• Procedure tubing and accessory sets for sterile field setup.

Operator & facility requirements

Use only by qualified personnel trained in imaging-guided breast biopsy. Follow institutional protocols for anticoagulation, sterile technique, specimen labeling, and pathology handoff. Contraindications and precautions follow manufacturer IFU and society guidelines applicable in your country.

Quality & compliance

Manufactured under a medical-device quality system orientation aligned with international market expectations. Marketing claims, CE/registration status, and catalog numbers must be confirmed for your territory before quotation.

Disclaimer

This page summarizes positioning for international lead generation. It does not replace the instructions for use, risk management file, or local regulatory labeling.