Mini Emergency Self Tapping Non-Locking Purple OD - 2.3 L - 8 - JEIL Medical

What is the Mini Emergency Self Tapping Purple OD - 2.3 L - 8 - JEIL Medical?

The Mini Emergency Self Tapping Purple OD - 2.3 L - 8, referenced under code 241.012308 by Jeil Medical, is an emergency screw for osteosynthesis. This non-locking device features a diameter of 2.3 and a length of 8. Its structure is specifically designed to offer an alternative fixation solution when the initial threading in the bone does not allow for optimal retention. It belongs to the range of solutions for guided bone regeneration (GBR) developed by Jeil Medical Corp, a recognized manufacturer in the field of implantology and maxillofacial surgery.

What are the clinical indications for this emergency screw?

This bone block fixation screw is primarily indicated in oral and implant surgery during reconstruction protocols. It serves as a bone surgery emergency screw when instability is observed with a smaller diameter screw. Its use is common in onlay grafting procedures, stabilization of autologous grafts, or the maintenance of barrier devices. As an emergency osteosynthesis screw, it allows the practitioner to secure the surgical assembly without having to completely change the drilling site, thus guaranteeing the durability of the bone graft.

What are the technical characteristics of this Jeil Medical device?

The Mini Emergency screw from Jeil Medical is distinguished by its self-tapping osteosynthesis screw property, facilitating its insertion into bone tissue. With an outer diameter (OD) of 2.3 and a length of 8, it offers an increased contact surface compared to standard screws. Its non-locking nature allows for a certain modularity during the application of the plate or block. The purple color code facilitates quick identification within the surgical kit. It is designed to meet the mechanical stability requirements necessary during the critical phases of subperiosteal bone healing.

What are the contraindications for the use of this screw?

Contraindications for the use of this emergency osteosynthesis screw include clinical situations where the residual bone volume is insufficient to accommodate a diameter of 2.3. As with any metallic fixation device, a history of hypersensitivity to the material components (generally titanium alloys in bone surgery) constitutes a major contraindication. It must not be used in sites presenting an active infection or severely compromised vascularization. It is the surgeon's responsibility to evaluate bone density to ensure that the self-tapping nature does not risk further weakening the recipient site.

What are the precautions related to handling and removal?

As a non-resorbable device, this fixation screw must be handled with gripping instruments adapted to the Jeil Medical range to avoid any deformation of the screw head. The practitioner must ensure that an appropriate insertion torque is respected despite its self-tapping function. Post-operative radiographic monitoring is recommended to verify the maintenance of stability. Removal of the screw generally occurs after the graft incorporation phase or during implant placement, according to the guided bone regeneration protocol established by the surgeon.

Who is the manufacturer and what standards are met?

The product is manufactured by Jeil Medical Corp., a company specializing in high-precision osteosynthesis devices. To obtain detailed information on the regulatory class, specific CE marking, or ISO standards for this specific model (reference 241.012308), it is imperative to refer to the product labeling and the instructions for use provided by the manufacturer. Jeil Medical ensures rigorous traceability of its medical devices, guaranteeing that each screw meets the quality standards required for safe and effective surgical implantation in the oral environment.

State of the art

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