Mid Emergency Self Tapping Purple OD - 1.8 L - 5 - JEIL Medical

What is the Mid Emergency Self Tapping Purple OD - 1.8 L - 5 - JEIL Medical?

The Mid Emergency Self Tapping Purple OD is a specialized device developed by Jeil Medical for Guided Bone Regeneration (GBR) interventions. This product is distinguished by its self-tapping design (Self Tapping), facilitating its insertion during surgical procedures. Identified under reference 241.011805 at Delynov, this purple-colored device (Purple) features a specific outer diameter and a length of 5mm (L - 5). It is designed to meet the needs of dental surgeons and implantologists seeking precise fixation solutions. Its structure is optimized to ensure effective primary stability in bone reconstruction protocols.

What are the clinical indications for this Jeil Medical device?

This Jeil Medical device is primarily indicated for oral surgery and implantology, specifically for Guided Bone Regeneration (GBR) procedures. Its use is recommended when stable fixation is required to maintain membranes or stabilize bone grafts. Thanks to its self-tapping tip, it allows for a less invasive approach during cortical penetration. Practitioners use this type of equipment to secure the architecture necessary for bone neoformation before or during the placement of dental implants, thus ensuring an optimal healing environment.

What are the technical characteristics of product 241.011805?

The Mid Emergency model from Jeil Medical features rigorous technical specifications for surgical practice. It has a diameter of 1.8mm (OD - 1.8) and a length of 5mm (L - 5). The 'Self Tapping' characteristic means that the thread is designed to create its own path in the bone, thereby reducing the need for intensive pre-drilling in certain bone densities. Its purple color (Purple) allows for quick visual identification and high contrast at the surgical site. These dimensions and mechanical properties are specifically calibrated to offer the tensile strength and holding stability essential in maxillofacial surgery.

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

Although detailed specifications are not provided here, the use of this Jeil Medical fixation device is generally contraindicated in patients with uncontrolled systemic pathologies affecting bone healing or calcium metabolism. It should not be used in the presence of an active infection at the surgical site or in cases of insufficient residual bone volume to ensure the anchoring of the device. Known allergies to the constituent materials (often metal alloys in bone surgery) also constitute a major contraindication. The surgeon must evaluate the patient's bone quality before any placement.

What are the precautions for use and handling?

Handling this Jeil Medical device requires adapted and sterile instrumentation. As a non-resorbable material intended for fixation, it must be placed with controlled tightening torque to avoid any neck fracture or excessive damage to the surrounding bone. Practitioners must ensure perfect axial insertion to maximize the self-tapping properties. Post-operative monitoring is essential to check for the absence of material exposure or soft tissue inflammation. It is recommended to strictly follow cleaning and sterilization protocols if the product is delivered non-sterile, in accordance with the manufacturer's instructions.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., an internationally recognized company in the sector of implants and surgical instrumentation. Regarding specific certifications, such as the regulatory class or CE marking, this information is not specified in the current technical documentation. It is the responsibility of healthcare professionals to systematically consult the instructions for use (IFU) and the labeling of the delivered product to verify compliance with current local and European standards. Jeil Medical ensures the traceability of its products via unique reference codes such as 241.011805.

State of the art

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