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

What is the Jeil Medical mesh punch?

The mesh punch for implantology and dental surgery, designed by Jeil Medical, is a specialized surgical instrument intended for the manipulation of bone regeneration devices. This tool is specifically developed to work on the thin metal structures used during bone grafts. As a gbr (Guided Bone Regeneration) instrument, it allows for modifying the structure of physical barriers to optimize their clinical integration. Its robust design by Jeil Medical Corp. ensures reliable handling during the critical preparation phases of bone support implants.

What are the clinical indications for this instrument?

This device is indicated in oral and implant surgery, particularly during ridge reconstruction procedures or the filling of bone defects. It is used as a gbr grid punch to adapt graft protection devices. The practitioner uses this instrument to create passage points or adjust the porosity of barrier materials. Its use is central in regeneration protocols where the use of a titanium grid punch is required to ensure stability and adequate vascularization of the operated site, thus promoting bone neoformation under the membrane.

What are the technical characteristics of the Jeil Medical punch?

The Jeil Medical mesh punch is distinguished by its ability to cleanly perforate rigid materials without excessive deformation of the overall structure. Although the exact composition specifications are not detailed, it is designed to meet the requirements of modern implant surgery. This titanium mesh punch offers a grip adapted to meticulous intraoral interventions. The mechanics of the instrument allow for a controlled application of force, essential for working on titanium alloys without compromising the integrity of the guided bone regeneration device.

What are the contraindications for the use of this punch?

The contraindications for the use of the Jeil Medical mesh punch are mainly related to clinical situations where the use of titanium grids or meshes is itself proscribed. This includes patients with known allergies to the constituent metals of the manipulated devices or serious systemic pathologies preventing bone healing. The use of this gbr instrument should not be considered if the device to be perforated is not compatible with mechanical modification, at the risk of altering its barrier properties or structural resistance. It is necessary to systematically refer to the manufacturer's specific surgical protocol.

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

As a reusable and non-resorbable surgical instrument, the Jeil Medical mesh punch requires a rigorous sterilization and decontamination protocol after each intervention. The practitioner must ensure the removal of all biological residues in the perforation mechanisms to maintain cutting efficiency. It is recommended to regularly check the alignment of the perforation jaws to guarantee the precision of the movement. Appropriate lubrication of the joints, in accordance with the recommendations of Jeil Medical Corp., helps extend the life of the instrument and ensure consistent performance during bone regeneration surgeries.

Who is the manufacturer and what standards are respected?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and dental implantology. The Jeil Medical brand is associated with industrial manufacturing standards for medical devices. Although the precise regulatory class and specific CE marking are not mentioned in the source documentation, this instrument is designed for professional use in a sterile environment. Practitioners are invited to consult the product labeling and the instructions for use provided by the manufacturer to obtain details regarding conformity certifications and current safety standards.

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