DePuy 1342-52 Kuntscher Nail Intramedullary Rod Double-Pointed 12mm x 38cm

DePuy 1342-52 Kuntscher Nail Intramedullary Rod Double-Pointed 12mm x 38cm

• Model: 1342-52
• Diameter: 12 mm
• Length: 38 cm (380 mm)
• Design: Double‑pointed
• Material: Stainless Steel
• Fixation Style: Classic non‑locking

The DePuy 1342‑52 Kuntscher Nail Intramedullary Rod (12 mm × 38 cm) is a precision‑manufactured orthopedic implant engineered to deliver reliable long bone fracture stabilization in trauma and reconstructive surgical procedures. Designed with double‑pointed ends for intuitive insertion, this intramedullary rod enables surgeons to guide and seat the implant securely within the medullary cavity, facilitating controlled anatomical alignment and structural support. Its optimized 12 mm diameter paired with a 38 cm length makes it suitable for a broad range of adult femoral and tibial diaphyseal applications where dependable internal fixation is critical.

Built with high‑quality biocompatible materials and crafted to exacting manufacturing standards, the DePuy 1342‑52 Kuntscher Nail exemplifies the dependable performance clinicians expect from premium orthopedic implants. The classic Küntscher nail design has a long heritage in internal fracture management and offers intrinsic biomechanical advantages by providing longitudinal support while sharing physiological loads with the host bone, which can help support early mobilization and reduce stress shielding during the healing process.

Backed by DePuy Synthes’ longstanding commitment to orthopedic innovation, this intramedullary rod is an effective solution for surgical teams managing acute long bone fractures. Whether used in closed reduction techniques or as part of comprehensive trauma care strategies, the DePuy 1342‑52 provides the consistent structural reliability and surgical versatility necessary for demanding clinical environments. Its proven design supports improved procedural efficiency and contributes to optimized outcomes in long bone fracture fixation.

This medical supply or implant item's original equipment manufacturer (OEM) packaging has been compromised or opened. While it remains unused, it is listed as non-sterile and sterilization will be required prior to use.