Mesh Plate 37 x 24 x 0.2mm - Jeil Medical,

What is the Jeil Medical 37 x 24 x 0.2mm mesh plate?

The 37 x 24 x 0.2mm mesh plate designed by Jeil Medical is a medical device intended for oral and maxillofacial surgery procedures. This device comes in the form of a specific mesh structure, providing structural support during reconstructive procedures. With precise dimensions of 37mm in length by 24mm in width and a thin thickness of 0.2mm, this Jeil Medical brand product allows for rigorous morphological adaptation. It belongs to the category of surgical consumables distributed by Delynov to meet the needs of implantologists and specialized surgeons seeking high-performance bone fixation and maintenance solutions.

What are the clinical indications for this Jeil Medical device?

This mesh plate from Jeil Medical is indicated for reconstructive surgery procedures, particularly in implantology and oral surgery. It is used by healthcare professionals to stabilize bone grafts or to maintain the structural integrity of surgical sites during bone regeneration. Its mesh design promotes integration and handling during complex surgeries requiring mechanical reinforcement. Practitioners use this type of Jeil Medical Corp. device to ensure a stable barrier or support, thereby facilitating the clinical success of guided bone reconstruction protocols or the repair of maxillary defects.

What are the technical characteristics of the 37 x 24 x 0.2mm plate?

The technical characteristics of this Jeil Medical product are based on its rigorous geometry. The plate features a surface area of 37 x 24 mm, offering extensive coverage for large bone defects. Its 0.2mm thickness is a critical parameter, allowing for the combination of mechanical strength necessary for tissue maintenance while remaining thin enough to limit sub-mucosal bulk and facilitate intraoperative modeling. The mesh structure allows for permeability and flexibility adapted to the complex anatomical contours encountered in oral surgery. Each unit is manufactured by Jeil Medical Corp. according to industrial precision standards to guarantee repeatability of performance during placement.

What are the contraindications for the use of this mesh plate?

The use of the Jeil Medical 37 x 24 x 0.2mm mesh plate is contraindicated in patients with known allergies to the metals or components of the device (refer to the manufacturer's technical notice for the exact composition). It must not be used in sites with active uncontrolled infection or insufficient vascularization that would compromise healing. As with any fixation device, poor oral hygiene or unstabilized systemic pathologies (such as uncontrolled diabetes) may constitute relative or absolute contraindications. The surgeon must evaluate the benefit-risk ratio based on the patient's overall health status before any implantation.

What are the precautions for use and removal procedures?

As a maintenance device, the Jeil Medical mesh plate requires strict aseptic handling. During placement, it is crucial to avoid excessive tension on the surrounding soft tissues to prevent risks of material exposure. In the event of post-operative exposure, rigorous clinical follow-up is essential. Regarding the fate of the device, if it is non-resorbable, a second intervention may be necessary for its removal after the bone consolidation phase, in accordance with the surgical protocol established by the practitioner. Precautions also include the choice of fixation screws compatible with the mesh dimensions to ensure optimal primary stability throughout the duration of the treatment.

Who is the manufacturer and what is the regulatory information?

The official manufacturer of this device is Jeil Medical Corp., a company globally recognized for its expertise in the design of osteosynthesis systems and solutions for maxillofacial surgery. Regarding specific certifications, such as the regulatory class or CE marking, as this information is not specified in the simplified technical documentation, it is imperative for the user to consult the product labeling and the instructions for use (IFU) provided by Jeil Medical before any use. Compliance with the sterilization and storage protocols indicated by the manufacturer is essential to guarantee patient safety and device efficacy during surgical interventions.

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