Handle screwdriver set - Jeil Medical (111-010) - Delynov

What is the ROGFIXE screwdriver handle - Jeil Medical (111-010)?

The ROGFIXE screwdriver handle, referenced under code 111-010 by Jeil Medical, is a manual instrument specifically developed for guided bone regeneration interventions. This device constitutes the main body onto which compatible screwdriver shafts are fitted. Manufactured by Jeil Medical Corp., this handle is designed to offer a firm and secure grip for dental surgeons and implantologists. Its structure is optimized to withstand the mechanical stresses associated with the fixation of fine osteosynthesis material, thus guaranteeing a stable interface between the practitioner's hand and the screwing insert.

What are the clinical indications for this surgical screwdriver handle?

This surgical screwdriver handle is indicated for all fixation phases within the framework of oral surgery and implantology. Its primary use concerns the placement of micro-fixation screws used to stabilize regeneration membranes or bone grafts (onlay or inlay). As a central element of the ROGFIXE system from Jeil Medical, it is used in alveolar reconstruction protocols where precision of manual tightening torque is required. It allows the practitioner to finely control the insertion of screws into complex anatomical sites, ensuring the primary stability essential for successful bone regeneration.

What are the technical characteristics of the 111-010 implantology screwdriver handle?

The implantology screwdriver handle bearing technical reference 111-010 is distinguished by its ergonomic design adapted to the requirements of micro-surgery. Although specific dimensions are not detailed, this Jeil Medical device is developed to allow fluid rotation and precise axial control. The internal connection mechanism is calibrated to effectively lock compatible inserts from the ROGFIXE system, avoiding any mechanical play during the operative act. Its surface is treated to facilitate cleaning and decontamination in a clinical environment, meeting the durability standards expected for reusable surgical instrumentation.

What are the contraindications for the use of this instrument?

The contraindications related to the use of the ROGFIXE screwdriver handle are mainly clinical and technical. The instrument must not be used for screwing applications requiring a tightening torque exceeding the manual capacities of the operator or the resistance limits of the associated screws. It is imperative not to use this handle with third-party inserts not validated by Jeil Medical, in order to avoid any risk of decoupling or material damage. As with any surgical instrument, its use is prohibited in the event of a failure in prior sterilization or the presence of signs of wear or corrosion on the body of the device.

What are the maintenance precautions for this non-resorbable equipment?

As a non-resorbable metallic surgical instrument, the dental screwdriver handle requires a rigorous maintenance protocol. After each implant surgery intervention, the device must be subjected to a complete cycle of pre-disinfection, manual or ultrasonic cleaning, and autoclave sterilization according to the parameters recommended by the manufacturer Jeil Medical Corp. It is essential to check for the absence of organic residues in the insert connection area. Periodic lubrication of moving parts, if applicable, must be performed with products compatible with steam sterilization to maintain the fluidity of the rotation mechanism.

Who is the manufacturer and what standards are respected?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of instrumentation for osteosynthesis and bone regeneration. The ROGFIXE screwdriver handle (111-010) is designed according to strict industrial manufacturing processes specific to high-precision medical devices. To obtain detailed information on the regulatory class, CE marking, or specific ISO certifications for this product, it is recommended to refer to the instructions for use provided by Jeil Medical or to consult the technical documentation available from Delynov. Compliance with use protocols guarantees the instrument's conformity with surgical safety requirements.

State of the art

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