Driver Tree J-Tac - Jeil Medical (113-JT-101) - Delynov

What is the J-Tac - Jeil Medical driver shaft (113-JT-101)?

The J-Tac driver shaft, bearing reference 113-JT-101, is a technical instrument designed by Jeil Medical. This specific device belongs to the J-Tac range from the brand Jeil Medical, recognized for its osteosynthesis and fixation solutions in surgery. As a component of the driver system, this shaft plays a central role in the handling and application of J-Tac fixation devices. Its design is optimized to integrate perfectly into the surgical protocol of demanding practitioners, offering a reliable interface between the surgeon's hand and the fixation elements during bone regeneration or membrane stabilization procedures.

What are the clinical indications for this Jeil Medical instrument?

The J-Tac driver shaft is primarily indicated for oral surgery, implantology, and maxillofacial surgery procedures requiring the use of the J-Tac system. It is used by healthcare professionals to facilitate the precise placement of tacks or fixation screws during guided bone regeneration (GBR) procedures. This instrument allows for the transmission of the movement necessary to anchor the maintenance devices, thus ensuring the stability of membranes or bone grafts. Its use is reserved for dental surgeons and stomatologists trained in the specific protocols of the Jeil Medical brand to guarantee optimal tissue integration.

What are the technical characteristics of reference 113-JT-101?

The 113-JT-101 model is distinguished by precision engineering specific to Jeil Medical Corp. standards. This driver shaft is specifically calibrated to be compatible with other elements of the J-Tac range. Its structure is designed to offer an ergonomic grip and controlled force transmission, thereby minimizing the risk of slipping during the insertion of fixations. Although detailed material specifications are not explicitly listed, this type of instrument is traditionally manufactured to meet the requirements for durability and repeated sterilization necessary in a surgical environment, ensuring increased longevity within the technical tray.

What are the contraindications for the use of this driver shaft?

Contraindications for the use of the J-Tac driver shaft are primarily related to inappropriate use or use outside the protocol defined by Jeil Medical. It must not be used with non-compatible fixation systems, as this could damage the instrument or compromise patient safety. Generally, the use of this instrument is prohibited in patients presenting systemic contraindications to oral surgery or the implantation of bone fixation devices. The practitioner must imperatively refer to the technical instructions from the manufacturer Jeil Medical Corp. to evaluate the specific risks related to each clinical case before any intervention.

What are the maintenance and handling precautions?

As a precision surgical instrument, the J-Tac driver shaft requires rigorous handling to maintain its performance. After each use, it must be cleaned and sterilized in accordance with current protocols for reusable medical devices, strictly following Jeil Medical's recommendations. The integrity of the connection (reference 113-JT-101) should be checked before each operative procedure to ensure the absence of wear or deformation. Storage in a dry and protected environment is essential to prevent any alteration of its mechanical properties, thus guaranteeing constant precision during critical bone fixation phases.

Who is the manufacturer and what standards are respected?

The J-Tac driver shaft (113-JT-101) is manufactured by Jeil Medical Corp., an international leader in the field of medical devices for bone surgery. Although specific certifications such as the regulatory class or CE marking are not detailed in the current source data, Jeil Medical is recognized for applying rigorous manufacturing standards. To obtain precise information on regulatory compliance, CE marking, or ISO certifications specific to this product, it is recommended that professionals consult the official documentation provided by the manufacturer or contact the Delynov technical service.

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