Mesh perforator for implantology and dental surgery - Jeil Medical - Delynov

What is the Jeil Medical mesh punch?

The Jeil Medical mesh punch is a specialized instrument designed for implantology and dental surgery. Developed by Jeil Medical Corp., this technical device allows for the precise preparation of surgical meshes before their placement. This product belongs to the consumables (CONSO) category distributed by Delynov. Its design aims to facilitate the work of practitioners during bone reconstruction or graft stabilization procedures, where mesh adaptation is a critical step for the success of the intervention.

What are the clinical indications in oral surgery?

The Jeil Medical mesh punch is primarily indicated during oral surgery and implantology procedures requiring the use of regeneration meshes. Its role is essential for adapting barrier devices to the patient's specific anatomical features. It is used by dental surgeons and implantologists to ensure clean and precise perforation of reinforcement materials, thus optimizing the integration of the mesh into the surgical site. This instrument meets the requirements of modern clinical protocols in pre-implant surgery.

What are the technical characteristics of this device?

The Jeil Medical mesh punch is distinguished by ergonomics adapted to meticulous manipulations in the oral area. As an instrument in the Jeil Medical range, it benefits from the expertise of Jeil Medical Corp. in the manufacture of devices for osteosynthesis and maxillofacial surgery. Although exact dimensional specifications are not detailed, its primary function is to guarantee consistent and burr-free perforation of the meshes, thus avoiding any deformation of the material during preoperative preparation.

What are the contraindications for the use of this instrument?

The use of the Jeil Medical mesh punch is contraindicated in situations where sterility protocols cannot be guaranteed or if the instrument shows signs of wear that could compromise cutting precision. It must not be used on materials for which it was not specifically designed by Jeil Medical Corp. Practitioners must systematically refer to the manufacturer's technical instructions to identify usage limits related to specific mesh materials or the patient's particular clinical conditions.

What are the precautions for use and maintenance?

To maintain the effectiveness of the Jeil Medical mesh punch, it is imperative to follow the cleaning and sterilization recommendations specific to precision surgical instruments. Careful handling is required to preserve the perforation mechanism. Healthcare professionals must inspect the instrument before each use to ensure the absence of residues or structural damage. As with any device used in implantology, compliance with asepsis protocols is fundamental to prevent the risk of cross-infection during the preparation phases of implants and meshes.

Who is the manufacturer and what is the regulatory information?

The official manufacturer of this device is Jeil Medical Corp., a recognized company in the medical device sector for dental and maxillofacial surgery. The product is marketed under the name Jeil Medical mesh punch. Regarding specific certifications, CE marking, and regulatory class, this information is not specified in the current technical documentation. It is the responsibility of users to consult the product labeling and the instructions for use provided by Jeil Medical to verify compliance with current standards before any clinical use.

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Surgical medical consumables play a decisive role in operative safety.