Mesh Plate 75 x 51 x 0.2mm - Jeil Medical

What is the 75 x 51 x 0.2mm mesh plate - Jeil Medical?

The 75 x 51 x 0.2mm mesh plate designed by Jeil Medical is a surgical device used in bone reconstruction or stabilization procedures. This product comes in the form of a mesh structure allowing for precise adaptation to the patient's anatomical contours. With dimensions of 75mm in length, 51mm in width, and a very thin thickness of 0.2mm, this device offers a balance between malleability and mechanical support. Manufactured by Jeil Medical Corp., this plate is specifically sized to meet the needs of surgeons requiring high-precision materials for their complex interventions.

What are the clinical indications for this device?

This mesh plate from Jeil Medical is primarily indicated for oral, maxillofacial, and implantology surgical procedures requiring structural support. It is used for maintaining bone grafts, repairing localized bone defects, or reconstructing thin bone walls. Its mesh structure promotes vascularization of surrounding tissues while ensuring a stable physical barrier. Practitioners favor this 75 x 51 x 0.2mm format for large treatment surfaces where material flexibility is essential to fit the complex shapes of the maxilla or mandible.

What are the technical characteristics of the Jeil Medical plate?

The major technical characteristics of this Jeil Medical product are based on its geometry and thinness. The plate features dimensions of 75 x 51mm, covering a significant surface area for extensive reconstructions. Its 0.2mm thickness is a critical asset: it allows for easy handling and custom cutting by the surgeon, while minimizing submucosal bulk to avoid tension during soft tissue closure. The mesh design ensures the porosity necessary for biological exchanges, facilitating integration of the surgical site while maintaining sufficient structural rigidity for the protection of bone volume.

What are the contraindications for the use of this plate?

The use of the Jeil Medical mesh plate is contraindicated in patients with known allergies to the metallic components of the device. It should not be used in sites with an active uncontrolled infection or insufficient vascularization of the surrounding soft tissues, which would compromise healing. Furthermore, this device is not intended to support direct functional mechanical loads without adequate underlying bone support. The surgeon must evaluate the patient's general health status, including metabolic pathologies affecting bone regeneration, before any implantation of this surgical material.

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

As a non-resorbable device, the Jeil Medical mesh plate requires total and stable coverage by soft tissues to prevent any post-operative exposure. The practitioner must ensure rigorous fixation using appropriate osteosynthesis screws to avoid any micromovement detrimental to osseointegration. Particular attention must be paid during the shaping of the plate: cut edges must be smoothed so as not to damage adjacent tissues. Regular post-operative follow-up is essential to monitor for the absence of inflammatory reaction or dehiscence, and removal of the device may be considered according to the clinical protocol established by the surgeon after consolidation.

Who is the manufacturer and what is the regulatory information?

The official manufacturer of this device is Jeil Medical Corp., a globally recognized company in the osteosynthesis solutions sector. Regarding the standards met and the regulatory class, specific information is not detailed in the current technical documentation provided. It is imperative for the user to systematically refer to the Instructions for Use (IFU) included in the Jeil Medical product packaging to verify current certifications, CE marking, as well as precise sterilization and storage instructions. Device traceability must be rigorously recorded in the patient file in accordance with health safety requirements.

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