Plaque mesh 37 x 24 x 0.1mm - Jeil Medical
The Plaque mesh en maille 37 x 24 x 0.1mm - Jeil Medical is a medical device manufactured by Jeil Medical Corp..
- Manufacturer: Jeil Medical Corp..
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Jeil Medical mesh plate?
The mesh plate developed by Jeil Medical is a micro-osteosynthesis device used in oral and maxillofacial surgery. This consumable comes in the form of a grid with dimensions of 37 x 24 mm and an extremely reduced thickness of 0.1mm. Its perforated structure is specifically designed to provide mechanical support while promoting the biological exchanges necessary for tissue neo-vascularization. This type of titanium mesh plate is preferred for its ability to be manually shaped by the surgeon to precisely adapt to the anatomy of the surgical site, thus ensuring optimal maintenance of the graft materials.
What are the clinical indications for this device?
This Jeil Medical device is indicated for guided bone regeneration (GBR) procedures requiring a rigid but permeable physical barrier. In implantology, it is used for the treatment of localized bone defects, horizontal or vertical ridge augmentation, and the protection of particulate grafts. As a bone regeneration grid, it prevents the invagination of soft tissues into the graft site while maintaining the space necessary for osteogenesis. Its use is particularly relevant during complex reconstructions where a traditional flexible membrane would not suffice to maintain the desired volume against muscular or gingival pressures.
What are the technical characteristics of this plate?
The technical specifications of this dental mesh plate are based on its 37 x 24 mm format, offering a generous working surface to cover extensive defects. The 0.1mm thickness is a critical parameter: it allows for exceptional malleability, facilitating cutting and bending without compromising structural strength. This thinness also limits the risks of soft tissue dehiscence postoperatively, a key success factor in implant surgery. The Jeil Medical mesh design ensures primary stability of the site while allowing fluid diffusion of nutrients and osteogenic cells through the grid perforations.
What are the contraindications for the use of this plate?
Contraindications for the use of this GBR titanium mesh plate include clinical situations where the patient has a known hypersensitivity to the metals constituting the device. It must not be used in the presence of an active infection at the surgical site or in patients with serious systemic disorders compromising bone or mucosal healing (local irradiation, uncontrolled diabetes, heavy smoking). Insufficient oral hygiene or inadequate soft tissue volume to completely cover the grid also constitute major contraindications, as early exposure of the plate can lead to regeneration failure.
What are the precautions related to its non-resorbable nature?
This titanium mesh plate is a non-resorbable device, meaning it maintains its structural integrity throughout the healing phase. Unlike resorbable membranes, it generally requires a second surgical intervention for removal once bone consolidation is achieved (often after 6 to 9 months depending on the clinical case). The practitioner must ensure rigid fixation, often using micro-screws, to avoid any micromovement. Particular attention must be paid to flap management to ensure airtight and tension-free closure, preventing any exposure of the reconstruction titanium grid which could compromise the final result.
Who is the manufacturer and what standards are respected?
The device is manufactured by Jeil Medical Corp., a manufacturer recognized worldwide for its expertise in osteosynthesis and implantology systems. As a technical product intended for specialized surgery, this plate meets high-precision medical industrial manufacturing standards. Although specific details of the regulatory class are not mentioned here, Jeil Medical products undergo rigorous quality controls. It is the responsibility of the healthcare professional to systematically check the integrity of the sterile packaging before use and to refer to the technical instructions provided by the manufacturer for all applicable certifications and sterilization protocols.
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Specifications
| Manufacturer | JEIL MEDICAL |
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