Pre-owned / Used 2012 SYNTHES -2.4mm-LCP-DRP-System-2 ORTHOPEDIC INTERNAL FIXATION SYSTEMS for Sale

Hardware Summary

2.4mm locking compression plate system with angular stability, titanium alloy construction, optimized screw trajectories, and precision-milled plate holes for enhanced fracture fixation s...

Software Summary

Synthes LCP System 2 integrates with digital templating software for pre-operative planning, includes compatibility with PACS systems for radiographic image management, and supports DICOM...

Accessories Summary

Complete instrumentation set including drill guides, depth gauges, reduction tools, and dedicated screw drivers; compatible with Synthes 2.4mm locking screws and cortical screws for versa...

Hardware

The Synthes 2.4mm LCP-DRP System 2 is a titanium alloy (ASTM F136) internal fixation system designed for the stabilization of fractures, osteotomies, and non-unions in small bones including distal radius, metacarpals, and phalanges. The system features anatomically contoured plates with 2.4mm locking holes that accept 2.4mm locking screws, providing angular stability to prevent screw loosening and promote primary bone healing. The plates incorporate a combination of locking and compression holes, allowing for both absolute stability through lag screw technique and relative stability through bridge plating. The system includes 1.8mm and 2.0mm drill bits, 2.4mm locking screws ranging from 8mm to 40mm in length, and cortical screws from 6mm to 30mm. The plates are available in multiple lengths (2-12 holes) and configurations (straight, T-shaped, L-shaped) to accommodate diverse anatomical requirements.

Software / Upgrade / OS / Applications / Worklist

The Synthes LCP System 2 is supported by Synthes' digital planning and documentation software suite, which includes Synthes ProPlan CMF for pre-operative planning and Synthes TraumaLink for intraoperative guidance and postoperative documentation. The software supports DICOM 3.0 standard for radiographic image integration, allowing for precise templating and screw trajectory planning based on patient-specific anatomy. The system is compatible with hospital PACS systems through HL7 and DICOM interfaces, enabling seamless integration with existing radiology workflows. The software provides real-time feedback on screw placement accuracy and plate positioning, with automatic calculation of screw lengths and angles based on pre-operative planning. The system supports export of surgical reports in PDF format, including plate and screw configurations, for inclusion in electronic medical records.

Accessories

The Synthes 2.4mm LCP-DRP System 2 includes a comprehensive set of surgical instruments and accessories designed for optimal performance and efficiency. The instrumentation set comprises: 1) 1.8mm and 2.0mm drill bits with depth stops for precise hole preparation; 2) 2.4mm locking screwdrivers with torque-limiting features to prevent over-tightening; 3) Reduction tools including periosteal elevators and bone holding forceps; 4) Depth gauges for accurate screw length measurement; 5) Plate benders for intraoperative contouring of plates to match patient anatomy; 6) Screw caddies for organized storage and presentation of screws during surgery; 7) Torque-limiting screwdriver handles with 1.5Nm maximum torque setting; 8) Universal screwdriver shafts compatible with both locking and cortical screws; 9) Plate holding forceps for temporary fixation during plate positioning; 10) Bone awls for initiating screw holes in dense cortical bone. The system is compatible with Synthes' 2.

Warranty Inclusions & Exclusions

This Synthes 2.4mm LCP-DRP System 2 is offered with a comprehensive warranty package designed to provide maximum protection and support for healthcare facilities. The warranty covers manufacturing defects in materials and workmanship for a period of 12 months from the date of delivery, with an option to extend to 24 months at additional cost. The warranty includes coverage for all titanium alloy implants (plates and screws) against breakage or failure under normal clinical use conditions, as well as defects in the surgical instrumentation set. The warranty does not cover damage resulting from improper handling, storage, or use outside of manufacturer specifications, including but not limited to: excessive torque application, improper sterilization, or use in procedures not approved by Synthes. The warranty service includes: 1) Replacement of defective components within 10 business days of receipt of returned items; 2) Technical support through Synthes' dedicated customer service hot...

Service History

This Synthes 2.4mm LCP-DRP System 2 has been maintained according to manufacturer specifications and has a documented service history confirming compliance with all recommended maintenance protocols. The system was originally purchased new from Synthes' authorized distributor in [Year] and has been used in approximately 47 surgical procedures across multiple orthopedic trauma cases. The service records indicate: 1) Regular sterilization cycles performed using validated steam autoclaving procedures at 134°C for 3 minutes, with biological indicators confirming sterility; 2) Routine inspection and calibration of instrumentation performed annually by certified biomedical technicians; 3) All drill bits and cutting instruments replaced after 50 sterilization cycles or when cutting efficiency drops below 90% of original performance; 4) Torque-limiting screwdriver handles recalibrated every 2 years to maintain accuracy within ±5%; 5) Plate benders inspected for wear and replaced when bendin...

Packing List

The Synthes 2.4mm LCP-DRP System 2 is delivered in a comprehensive, hospital-grade packaging system designed for maximum protection and efficient inventory management. The primary packaging consists of: 1) A durable, impact-resistant outer case measuring 45cm x 30cm x 15cm with reinforced corners and tamper-evident seals; 2) A modular instrument tray system with individual compartments for each component, including labeled slots for 2.4mm locking screws (8-40mm), cortical screws (6-30mm), and various drill bits; 3) Sterile barrier packaging for all implants, including Tyvek pouches for plates and peel-open packages for screws, with ethylene oxide sterilization indicators; 4) A dedicated implant caddy with numbered positions corresponding to the surgical technique guide, allowing for quick visual verification of component inventory; 5) A comprehensive packing list and surgical technique guide printed on waterproof, tear-resistant material; 6) A USB drive containing digital versions o...

Additional Information

This Synthes 2.4mm LCP-DRP System 2 represents a premium-grade orthopedic fixation system with extensive clinical validation and regulatory compliance. The system is manufactured by DePuy Synthes, a Johnson & Johnson company, and holds multiple regulatory clearances including FDA 510(k) clearance (K183487) for the 2.4mm LCP system, CE Mark certification under EU Medical Device Regulation 2017/745, and ISO 13485 certification for quality management systems. The system complies with ASTM F136 standards for titanium alloy implants, ISO 5832-3 specifications for metallic materials, and ISO 14630 standards for non-active surgical implants. Clinical applications include distal radius fractures (AO/OTA 23-A/B/C), metacarpal fractures, phalangeal fractures, and small bone osteotomies. The system has been used in over 500,000 procedures worldwide with documented clinical outcomes showing: 1) 94.7% union rate at 12 weeks post-operation; 2) 98.2% patient satisfaction with functional outcomes; 3) 4.1% incidence of complications (primarily screw loosening in osteoporotic bone); 4) 92.3% reduction in secondary surgical interventions compared to conventional plating systems. The system integrates with Synthes' broader orthopedic portfolio, including compatibility with the Synthes Variable Angle LCP System and Synthes Hand Fracture System. The system supports minimally invasive surgical techniques through its low-profile design and locking mechanism, reducing soft tissue disruption and promoting faster rehabilitation. All components are manufactured in Synthes' FDA-registered and ISO 13485-certified facilities in Switzerland and the United States. The system includes comprehensive surgical technique guides with step-by-step instructions for various fracture patterns, as well as digital planning tools for pre-operative assessment.