Training Tree J-Tac - Jeil Medical (113-JT-103) - Delynov Dental Surgery Products

What is the J-Tac drive shaft - Jeil Medical?

The J-Tac drive shaft, bearing reference 113-JT-103, is a mechanical transmission device designed by Jeil Medical Corp. This component is specifically developed to integrate into the J-Tac surgical protocol. As a precision accessory, it serves as an interface between the gripping instrumentation and the fixation screws or pins used in oral surgery. Its design aims to ensure a stable connection and optimal torque transmission, thereby guaranteeing secure handling of micro-components during the critical fixation phases of bone regeneration devices. This product belongs to the category of technical consumables for advanced implantology.

What are the clinical indications for this drive shaft?

The use of this surgical drive shaft is indicated during oral surgery and implantology procedures requiring the placement of bone fixation systems. It is particularly requested in Guided Bone Regeneration (GBR) protocols for the installation of membrane stabilization screws or pins. Practitioners use this GBR screw drive shaft to accurately deliver and fix structural support elements in areas of bone deficit. Its role is crucial for ensuring the primary stability of barrier devices, a sine qua non condition for successful osseointegration and predictable volumetric reconstruction of alveolar ridges.

What are the technical characteristics of reference 113-JT-103?

The drive shaft referenced 113-JT-103 by Jeil Medical is characterized by a specific geometry adapted to the J-Tac system. As a screwdriver drive shaft, it features a connection end calibrated to fit perfectly into the screw or pin heads of the same range, thus avoiding any deleterious mechanical play. Its structure is designed to withstand the torsional stresses encountered during screwing into cortical bone. Although exact material specifications are not detailed in the source data, this type of accessory is generally developed to meet the biocompatibility and mechanical strength requirements specific to high-precision surgical instrumentation in implantology.

What are the contraindications for the use of this device?

The contraindications related to the use of this pin drive shaft are primarily clinical and technical. It must not be used outside the J-Tac system from Jeil Medical for which it was specifically designed, to avoid any risk of mechanical failure or damage to components. Medically, the use of this device is prohibited in patients with general contraindications to oral surgery or implantology, such as uncontrolled bone pathologies or severe healing disorders. The practitioner must ensure the absence of known allergies to the metallic components of the instrumentation before any intervention.

What are the precautions for use and maintenance?

Like any implant screwdriver accessory, the J-Tac drive shaft requires rigorous handling to maintain its performance. Before each use, it is imperative to check the physical integrity of the connection to prevent any risk of component detachment in the mouth. As a device used in a sterile environment, strict compliance with the cleaning, disinfection, and sterilization protocols recommended by the manufacturer Jeil Medical Corp is essential. Excessive wear of the shaft tip can compromise torque transmission; it is therefore recommended to replace the part as soon as signs of mechanical fatigue appear to guarantee patient safety and surgical precision.

Who is the manufacturer and what standards are respected?

The J-Tac drive shaft is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and implantology. Although the specific regulatory class and CE marking are not explicitly mentioned in the provided technical documentation, Jeil Medical brand products are developed according to high quality standards specific to surgical medical devices. As a distributor, Delynov ensures that these consumables meet the necessary safety requirements for use in dental offices or operating rooms. For any precise information on certifications or ISO standards in force for this code 113-JT-103, please refer to the technical instructions provided by the manufacturer.

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