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

What is the ROGFIXE screwdriver handle - Jeil Medical?

The ROGFIXE screwdriver handle, referenced under code 111-010, is a central manual instrument in guided bone regeneration protocols. Manufactured by Jeil Medical Corp., this surgical screwdriver handle serves as an ergonomic support for various driving tips. Its structure is specifically designed to provide a stable grip for dental surgeons and implantologists during critical phases of fixing osteosynthesis hardware. It constitutes the main interface between the practitioner's hand and the fixation screws, guaranteeing precise axial force transmission during anchoring in the maxillary or mandibular bone tissues.

What are the clinical indications for this instrument?

This Jeil Medical instrument is indicated for all oral surgery interventions requiring the use of micro-screws or fixation screws. In implantology, it is used for the stabilization of barrier membranes, titanium meshes, or autogenous and allogeneic bone grafts. Its role is crucial in guided bone regeneration (GBR) where the primary stability of the regeneration material determines the success of osseointegration. The handle allows for controlled screwing in areas with sometimes restricted access, thus facilitating alveolar ridge augmentation or sinus lift procedures.

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

The ROGFIXE screwdriver handle is distinguished by its exclusive compatibility with the Jeil Medical micro-screw system. Although specific materials are not detailed, this type of dental screwdriver handle is designed to withstand repeated sterilization cycles in an autoclave. Its technical design is based on a secure connection mechanism allowing screwdriver shafts to be clipped or inserted without mechanical play. The design of the handle body is optimized to prevent surgical gloves from slipping, thus ensuring fluid rotation and constant pressure when engaging the screw into the cortical bone.

What are the contraindications for the use of this device?

The contraindications related to the use of this surgical screwdriver handle are mainly clinical and technical. It must not be used outside the indications provided by Jeil Medical Corp., particularly with incompatible tips or screws that could damage the screw thread or the locking mechanism. Medically, use is contraindicated if the surgical site presents an untreated active infection or if the bone density is insufficient to guarantee the hold of the screws inserted via this instrument. The practitioner must ensure the absence of known allergies to the metallic components of the surgical instrumentation before any intervention.

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

As a reusable and non-resorbable surgical instrument, the ROGFIXE screwdriver handle requires a rigorous decontamination and sterilization protocol after each procedure. It is imperative to follow the manufacturer Jeil Medical's recommendations regarding manual or ultrasonic cleaning to eliminate any organic residue in the junction areas. Periodic lubrication of moving parts may be necessary if specified in the technical instructions. Storage must be in a dry and protected environment to avoid any corrosion. Before each surgery, the integrity of the insert fixation mechanism must be checked to ensure patient safety.

Who is the manufacturer and what standards are met?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of maxillofacial and dental osteosynthesis. Regarding regulatory certifications such as the risk class or specific CE marking, this information is not specified in the current technical documentation. It is the responsibility of the healthcare professional to consult the instructions for use attached to the product (reference 111-010) and to check the official labeling to confirm compliance with the European standards in force (MDR). The reputation of Jeil Medical is based on providing high-precision instruments intended for the requirements of modern implant surgery.

State of the art

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