Micron Screw Block and Mesh Plate - Jeil Medical (112-060) - Delynov

What is the Micro-screw and Mesh plate block - Jeil Medical (112-060)?

The Micro-screw and Mesh plate block, referenced under code 112-060, is a specialized device designed by Jeil Medical for Guided Bone Regeneration (GBR) interventions. This system is specifically developed to meet the needs of dental surgeons and implantologists during complex bone reconstruction procedures. It consists of a set of micro-screws and a mesh structure, allowing for precise stabilization and optimal maintenance of graft materials. The Jeil Medical brand is recognized for the precision of its components, offering practitioners a reliable technical solution to secure the bone volumes necessary for subsequent implant placement.

What are the clinical indications for this Jeil Medical device?

The Jeil Medical micro-screw and mesh plate block (112-060) is primarily indicated for oral surgery and implantology. Its use is recommended for Guided Bone Regeneration (GBR) procedures, where it is necessary to maintain a membrane or a mesh plate to protect the graft site. This device allows for the mechanical fixation of support structures to prevent any displacement of bone substitutes during the healing phase. It is particularly suitable for alveolar ridge augmentations and reconstructions of localized bone defects, ensuring the primary stability essential for successful bone integration.

What are the technical characteristics of reference 112-060?

The kit referenced 112-060 by Jeil Medical is distinguished by the optimized design of its micro-screws and mesh plate. Although specific dimensions are not detailed here, this technical block is designed to offer easy handling and rigid fixation. The micro-screws are developed to integrate perfectly with the mesh plate, guaranteeing a stable assembly under the soft tissues. This fixation system is a key element for practitioners seeking high-precision equipment for hard tissue management in implant surgery, allowing for fine anatomical adaptation according to the specific needs of the surgical site.

What are the contraindications for the use of this GBR material?

The use of the Jeil Medical micro-screw and mesh plate block must be carefully evaluated by the surgeon. General contraindications include situations where the patient's health status does not permit oral surgical intervention (uncontrolled coagulation disorders, serious systemic pathologies). Locally, an active infection at the surgical site, insufficient oral hygiene, or compromised tissue vascularization constitute major contraindications. It is imperative to systematically refer to the technical instructions from the manufacturer Jeil Medical Corp. to identify all specific exclusions related to the use of these bone fixation components.

What precautions should be taken for this non-resorbable device?

As a micro-screw and mesh plate type device, these elements are generally non-resorbable and intended to maintain the structure during the regeneration period. The practitioner must ensure total coverage by soft tissues to avoid any exposure of the material, which could lead to infectious complications. Particular attention must be paid during placement to ensure perfect stability without excessive tension on the flaps. Post-operative follow-up is crucial to monitor for the absence of inflammation. Removal of the material must be planned by the surgeon once the bone regeneration objective is achieved, in accordance with standard clinical protocols.

Who is the manufacturer and what standards are met for this product?

The official manufacturer of this device is Jeil Medical Corp., an internationally renowned company specializing in fixation systems for maxillofacial and dental surgery. Regarding specific standards and certifications, such as CE marking or the regulatory class of reference 112-060, information is not specified in the current technical documentation. Healthcare professionals are invited to consult the product labeling as well as the instructions for use provided by Jeil Medical to verify regulatory compliance data and current certifications before any clinical use in a practice or hospital setting.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.