Mesh Plate 75x51x0.1mm - Jeil Medical

What is the 75x51x0.1mm Jeil Medical mesh plate?

The 75x51x0.1mm mesh plate developed by Jeil Medical is a surgical device used in bone reconstruction or stabilization procedures. This product comes in the form of a fine mesh structure, providing an adaptable solution for practitioners. With a thickness of 0.1mm, this mesh allows for precise manipulation while maintaining the structural integrity required for oral and maxillofacial surgery interventions. As a product of the Jeil Medical range, this plate is designed to meet the requirements of specialized clinical environments, providing an interface between tissues and bone structures during healing phases.

What are the clinical indications for this device?

This mesh plate is primarily indicated for guided bone regeneration (GBR) procedures and the reconstruction of complex bone defects in implant and oral surgery. Its design allows for maintaining the volume of bone grafting materials and serves as a physical barrier or structural support. Dental surgeons and implantologists use this type of Jeil Medical device to stabilize grafts or to reinforce specific anatomical areas requiring rigid yet malleable containment. It is particularly suitable for cases of significant bone resorption where a supporting architecture is essential for the success of subsequent implant placement.

What are the technical characteristics of the plate?

The technical characteristics of this Jeil Medical model are based on its precise dimensions of 75x51mm, offering a generous working surface to cover extensive surgical sites. The ultra-thin thickness of 0.1mm is a major asset, allowing for easy cutting and optimal anatomical adjustment without creating excessive bulk under the soft tissues. Its mesh structure promotes the diffusion of biological fluids, which is essential for the vascularization of the operated site. The geometry of the plate is designed to offer a balance between flexibility during shaping and rigidity after fixation, thus ensuring the maintenance of the space necessary for bone neoformation.

What are the contraindications for the use of this plate?

The use of the 75x51x0.1mm mesh plate is contraindicated in patients with known allergies to the metallic components of the device. It must not be implanted in sites presenting an active infection or insufficient vascularization of the surrounding tissues. Furthermore, its use is discouraged if the patient suffers from serious systemic pathologies that could compromise bone or mucosal healing, such as certain uncontrolled metabolic disorders. It is the practitioner's responsibility to evaluate the benefit-risk ratio based on the patient's general health status and the quality of the recipient site before any surgical intervention.

What are the precautions for use and handling?

When handling this non-resorbable device, it is imperative to ensure rigorous asepsis to prevent any risk of intraoperative contamination. The plate must be shaped with appropriate instruments to avoid creating sharp edges that could perforate the mucosal flaps during closure. Particular attention must be paid to the fixation of the mesh to ensure its primary stability, as any micromovement can hinder the regeneration process. Coverage by soft tissues must be total and tension-free to limit the risks of post-operative exposure. Regular clinical follow-up is essential to monitor the integration of the device and the absence of inflammatory complications.

Who is the manufacturer and what is the regulatory information?

The device is manufactured by Jeil Medical Corp., a globally recognized player in the design of osteosynthesis solutions and surgical equipment. Regarding specific certifications, regulatory class, CE marking, or exact ISO standards, this information is not specified in the current simplified technical documentation. It is therefore strictly recommended that healthcare professionals consult the Instructions for Use (IFU) and the product labeling provided by Jeil Medical before any clinical use. These official documents contain all compliance data, sterilization protocols, and safety instructions essential for the proper use of the device in a surgical environment.

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