Screwdriver tree for screwdriver handle - Jeil Medical (113-MD-101) - Delynov

What is the ROGFIXE screwdriver shaft from Jeil Medical?

The screwdriver shaft for the ROGFIXE screwdriver handle, referenced under code 113-MD-101, is an interchangeable instrument designed by Jeil Medical Corp. This removable component fits onto a specific manual handle to form a complete screwdriver intended for handling fixation screws within the framework of oral and maxillofacial surgery. As part of the GBR (Guided Bone Regeneration) range, this shaft ensures the connection between the practitioner's hand and the screw head. Its robust design allows for controlled and secure insertion of the micro-screws required to maintain regeneration devices. Jeil Medical manufactures this instrument to meet the precision requirements of surgical environments.

What are the clinical indications for this surgical screwdriver shaft?

The surgical screwdriver shaft is primarily indicated for pre-implant bone reconstruction procedures. It is used by dental surgeons and implantologists for the placement of fixation screws during block bone grafts or the stabilization of regeneration membranes. This instrument is essential for fixing devices that maintain the bone volume necessary for future implant placement. Its use is part of GBR protocols where the primary stability of the membrane or bone block is crucial for the success of osseointegration. Thanks to its compatibility with the ROGFIXE handle from Jeil Medical, it offers a manual solution adapted to the restricted spaces of the oral cavity.

What are the technical specifications of reference 113-MD-101?

Technical reference 113-MD-101 corresponds to a screwdriver shaft designed by Jeil Medical Corp. This instrument is characterized by a working end calibrated to perfectly fit the screw heads of the GBR range. Although exact dimensions are not specified, this type of screwdriver blade is generally available in micro or mid configurations to match different bone fixation screw diameters. Its structure is optimized to transmit precise manual tightening torque without damaging the screw head. The fit between the shaft and the ROGFIXE screwdriver handle guarantees axial stability during rotation, thus minimizing the risk of slipping during the surgical act.

What are the contraindications for the use of this manual screwdriver tip?

The contraindications for the use of this manual screwdriver tip are primarily related to the limitations of the bone fixation procedures themselves. It must not be used if the recipient site presents an active infection or insufficient vascularization compromising the graft intake. Furthermore, the use of this instrument is prohibited with screws whose drive is not strictly compatible with reference 113-MD-101 from Jeil Medical, at the risk of generating metallic debris or stripping the screw. Patients with known allergies to metals used in surgical instrumentation (generally stainless steel alloys) also constitute a contraindication. It is the practitioner's responsibility to evaluate bone density to avoid any material fracture.

What are the maintenance and durability precautions for this instrument?

As a reusable surgical instrument, the Jeil Medical screwdriver shaft must undergo a rigorous cleaning, disinfection, and sterilization protocol after each use, in accordance with the manufacturer's instructions. It is recommended to visually inspect the tip of the screwdriver blade before each intervention to detect any signs of wear, bending, or corrosion. A blunt or deformed tip can compromise screw retention and must lead to the immediate replacement of the shaft. Storage must be carried out in a dry and clean environment. Although designed for long life, the precision of this instrument depends on compliance with the sterilization cycles recommended by Jeil Medical Corp.

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

The ROGFIXE screwdriver shaft (113-MD-101) is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of maxillofacial and dental osteosynthesis. Although specific details of the CE marking or regulatory class are not provided in the current documentation, this device is designed according to the industrial quality standards specific to surgical instruments. As a product distributed by Delynov, it is intended exclusively for professional use by practitioners trained in oral surgery techniques. For any precise information regarding regulatory certifications or ISO standards applied to the manufacturing process, it is imperative to refer to the product labeling and the technical instructions provided by Jeil Medical.

State of the art

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