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J-Tac Cap for Screwdriver Body - Jeil Medical (J-TAC CAP) - Delynov

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The J-Tac Cap pour Corps de Tournevis - Jeil Medical (J-TAC CAP) is a medical device manufactured by Jeil Medical Corp..

  • Manufacturer: Jeil Medical Corp..
  • Reserved for healthcare professionals. Read instructions carefully before use.

6.09 € 6.09 EUR 6.09 € Tax Included 8.34 €

6.09 € Tax Included 8.34 €

(0.00 € / Units)
  • Manufacturer

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GBR

What is the J-Tac Cap for Screwdriver Body?

The J-Tac Cap, designed by Jeil Medical, is a specific accessory intended to be mounted on the screwdriver body used in guided bone regeneration (GBR) protocols. This surgical screwdriver cap acts as a protective and holding interface for instruments in the J-Tac range. Its structure is developed by Jeil Medical Corp. to guarantee perfect compatibility with their anchorage systems. As a precision accessory, it allows for the securing of the rotating or manual elements of the screwdriver when they are not in direct contact with the surgical site, thus preventing any contamination or mechanical damage to the fine instrumentation.

What are the clinical indications for this accessory?

The use of the J-Tac Cap is indicated during oral surgery and implantology procedures requiring the fixation of membranes or bone blocks via the J-Tac system. This implantology screwdriver accessory is particularly useful during preparation phases where the practitioner must handle several components sequentially. It facilitates bone anchorage management by providing protection to the screwdriver body between two screwing steps or during the transfer of instrumentation. Its use is part of GBR protocols aimed at stabilizing filling materials or protective barriers against soft tissues.

What are the technical characteristics of the J-Tac Cap?

The J-Tac Cap (reference J-TAC CAP) features design characteristics specific to the Jeil Medical ecosystem. It is a surgical motor or manual screwdriver accessory distinguished by its precise fit on the instrument body. Although material specifications are not detailed here, it is designed to withstand standard sterilization cycles required in a surgical environment. Its ergonomic shape allows for rapid placement and removal, optimizing operative time during critical phases of fixing osteosynthesis nails or screws. It ensures the operational continuity of the J-Tac system without interfering with the gripping mechanism.

What are the contraindications for using this cap?

Contraindications for the use of the J-Tac Cap are primarily related to system incompatibility. It must not be used with screwdriver bodies from manufacturers other than Jeil Medical Corp., as an imperfect fit could compromise the safety of the surgical procedure. Generally, the use of this accessory is contraindicated if the device shows visible signs of wear, deformation, or corrosion that could alter its fixation. As with any osteosynthesis accessory, failure to comply with cleaning and sterilization protocols constitutes a major contraindication to its use in the operating room.

What are the precautions for use and maintenance?

To ensure the longevity of the J-Tac Cap, it is imperative to follow the cleaning recommendations provided by Jeil Medical. Before each intervention, the practitioner must check the integrity of the surgical screwdriver cap. After use, the device must undergo a complete decontamination and sterilization cycle. This accessory should be handled with care to avoid any drops that could distort the fit tolerances with the screwdriver body. Particular attention should be paid to storage to avoid any contact with corrosive chemical agents that could degrade the accessory's surfaces.

Who is the manufacturer and what standards are met?

The J-Tac Cap is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of instrumentation for maxillofacial surgery and implantology. Although the specific regulatory class and CE marking are not mentioned in this technical sheet, this product is designed according to the brand's rigorous quality standards to meet the requirements of healthcare professionals. For any precise information regarding regulatory certifications or ISO standards applied to this specific lot, it is recommended to consult the instructions for use attached to the product or to contact the Delynov technical service directly.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer JEIL MEDICAL
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GBR