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Mesh Plate 49 x 37 x 0.2mm - Jeil Medical

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The Plaque en maille 49 x 37 x 0.2mm - Jeil Medical is a medical device manufactured by Jeil Medical Corp..

  • Manufacturer: Jeil Medical Corp..
  • Reserved for healthcare professionals. Read instructions carefully before use.

61.05 € 61.05 EUR 61.05 € Tax Included 97.34 €

61.05 € Tax Included 97.34 €

(0.00 € / Units)
  • Manufacturer

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GBR

What is the 49 x 37 x 0.2mm mesh plate - Jeil Medical?

The mesh plate developed by Jeil Medical is a technical device used in reconstructive surgery. Presented in the form of a titanium mesh plate, it has dimensions of 49 x 37 mm with a very thin thickness of 0.2mm. Its perforated structure is specifically designed to allow optimal diffusion of biological fluids while ensuring a rigid physical barrier. This type of material is common in alveolar volume reconstruction protocols where mechanical stability is required to protect the filling material during the bone healing phase.

What are the clinical indications for this surgical mesh plate?

This dental surgery titanium plate is primarily indicated for large-scale guided bone regeneration (GBR) procedures. It is used by oral surgeons and implantologists to treat severe vertical or horizontal bone defects that require space maintenance that soft membranes cannot provide alone. Its application allows for the stabilization of autologous grafts or bone substitutes, thus preventing the collapse of soft tissues into the surgical site. It is particularly useful during pre-implant reconstructions aimed at restoring a sufficient alveolar ridge for the subsequent placement of implants.

What are the technical characteristics of this device?

The Jeil Medical device is distinguished by its generous 49 x 37 mm format, allowing it to cover wide surgical areas or be cut according to the specific needs of the site. With a thickness of 0.2mm, this titanium mesh plate offers a balance between structural rigidity and malleability, facilitating its adaptation to the curvatures of the maxillary or mandibular bone. The mesh design promotes vascularization of the underlying graft, a critical factor for regeneration success. Its manufacture by Jeil Medical Corp. ensures constant geometric precision, essential for stable fixation by osteosynthesis micro-screws.

What are the contraindications for the use of this dental surgery titanium grid?

Although specific data are not detailed here, general contraindications for this type of dental titanium mesh include known allergies to metals, particularly titanium or its alloys. Its use is discouraged in patients with uncontrolled systemic pathologies affecting bone healing, such as unbalanced diabetes or severe osteoporosis treated with certain bisphosphonates. Insufficient oral hygiene or an active infection at the operative site also constitute major contraindications. It is the practitioner's responsibility to evaluate the benefit/risk ratio based on the patient's general health status before any implantation.

What are the precautions related to the non-resorbable nature of the product?

This dental surgery titanium plate is a non-resorbable device. Unlike collagen membranes, it does not degrade in the body and must generally be the subject of a second surgical intervention for its removal once bone consolidation is achieved (often after several months). The main precautions concern the exposure of the plate: a hermetic closure of the soft tissues without tension is imperative to avoid any dehiscence. In case of early exposure in the oral environment, rigorous management of asepsis is necessary to prevent infection of the graft site, which could lead to the premature removal of the Jeil Medical device.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., a recognized company in the sector of osteosynthesis and solutions for maxillofacial surgery. Although specific certifications such as CE marking or regulatory class are not mentioned in the current source data, Jeil Medical products are usually designed according to strict international quality standards for implantable medical devices. To obtain precise information on regulatory compliance, ISO certificates, or detailed instructions for use (IFU), it is recommended to refer to the technical documentation provided by the manufacturer with the product or to contact the technical service directly.


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Manufacturer JEIL MEDICAL
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