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

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The Arbre d'entraînement J-Tac - Jeil Medical is a medical device manufactured by Jeil Medical Corp..

  • Manufacturer: Jeil Medical Corp..
  • Reference: 113-JT-103.
  • Reserved for healthcare professionals. Read instructions carefully before use.

100.52 € 100.52 EUR 100.52 € Tax Included 137.71 €

100.52 € Tax Included 137.71 €

(0.00 € / Units)
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GBR

What is the Jeil Medical J-Tac drive shaft?

The J-Tac drive shaft, referenced under code 113-JT-103, is a surgical instrumentation consumable developed by Jeil Medical. This device is specifically designed to serve as an interface between the surgical motor and the fixation elements used during bone reconstruction protocols. As part of the J-Tac range, this tool meets the requirements of practitioners specialized in oral surgery for the precise handling of stabilization components. Its design allows for efficient transmission of the torque required during critical clinical phases, thus ensuring fluid integration into the implant workflow.

What are the clinical indications for this instrument?

This drive shaft is primarily indicated for guided bone regeneration (GBR) surgeries and advanced implantology. It is used by dental surgeons and stomatologists for the activation and placement of bone fixation devices. Its role is central during the placement of membrane maintenance systems or graft stabilization. As a GBR screw drive shaft, it ensures the secure placement of fixation screws or pins in recipient sites, whether for horizontal or vertical bone defect filling prior to implant placement.

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

Reference 113-JT-103 corresponds to a standardized drive shaft within the Jeil Medical J-Tac system. This implant screwdriver mandrel is designed to fit conventional surgical contra-angles. Its geometry is optimized to ensure a stable connection and limit mechanical play during rotation. Although specific dimensions are not detailed in the primary technical sheet, this type of surgical drive shaft is manufactured to withstand the mechanical stresses encountered during insertion into cortical bone. The surface finish and machining precision signed by Jeil Medical Corp guarantee perfect compatibility with other instruments in the J-Tac range.

What are the contraindications for the use of this device?

The contraindications related to the use of the J-Tac drive shaft are primarily clinical and technical. Its use is prohibited in cases of systemic bone pathology preventing any oral surgical intervention or in cases of active infection at the operative site. Technically, it must not be used with incompatible fixation systems or motors that do not comply with the torque limits recommended by Jeil Medical. It is imperative that the practitioner verifies the integrity of the instrument before each use, as any deformation or excessive wear constitutes a contraindication to its use to avoid any risk of breakage or tissue damage.

What are the maintenance precautions for this non-resorbable material?

As a non-resorbable metallic instrument, the drive shaft requires a rigorous decontamination and sterilization protocol between each patient, in accordance with the manufacturer's guidelines from Jeil Medical. Practitioners must ensure thorough cleaning of connection areas to eliminate any organic residue. It is recommended to use neutral pH cleaning solutions to preserve the material's integrity. After the autoclave sterilization cycle, a visual inspection is necessary to ensure the absence of corrosion. Appropriate lubrication of moving parts, if specified by the instructions, may be required to maintain the fluidity of the implantology drive shaft.

Who is the manufacturer and what standards are respected?

The product is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and precision surgical instrumentation. Although the regulatory class and specific CE marking are not detailed in this document, devices produced by Jeil Medical are generally designed according to strict international quality standards for medical devices. To obtain precise information on the MDR classification or current ISO certifications for reference 113-JT-103, it is advised to refer to the product labeling and the instructions for use provided by Jeil Medical upon purchase from Delynov.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer JEIL MEDICAL
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GBR