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, is a precision manual instrument designed by Jeil Medical. This medical device is specifically developed for Guided Bone Regeneration (GBR) procedures. As a central element of the surgical instrumentation, this handle allows practitioners to manipulate various compatible inserts with control. The brand Jeil Medical ensures an ergonomic design to facilitate handling during delicate oral surgery interventions. This instrument is an essential component for professionals seeking reliable tools for placing fixation or osteosynthesis screws within the framework of bone reconstructions.

What are the clinical indications for this instrument?

The ROGFIXE screwdriver handle from Jeil Medical is indicated for oral surgery, implantology, and periodontology procedures requiring precise manipulation of fixation screws. It is primarily used during Guided Bone Regeneration (GBR) protocols to stabilize membranes or fix bone blocks. This instrument allows for the manual transmission of the necessary torque, thus offering optimal tactile sensitivity to the dental surgeon or maxillofacial surgeon. Its use is reserved for healthcare professionals trained in bone reconstruction techniques using the ROGFIXE system from Jeil Medical.

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

The ROGFIXE screwdriver handle (reference 111-010) is distinguished by its robustness and its compatibility with the Jeil Medical range of instruments. It is designed to receive screwdriver blades or inserts specific to the bone fixation system. Its structure is engineered to offer maximum ergonomics, allowing for fluid rotation and precise control during screw insertion. Although exact dimensions are not specified, its design meets operating room requirements in terms of durability and sterilization. This instrument integrates perfectly into the technical tray of practitioners specializing in implant and reconstructive surgery.

What are the contraindications for the use of this instrument?

The use of the ROGFIXE screwdriver handle is contraindicated in situations where oral surgery protocols cannot be respected. It must not be used with components or inserts that are not compatible with the Jeil Medical system, at the risk of damaging the instrument or compromising the safety of the surgical act. Generally, the use of this instrument is prohibited in patients presenting systemic contraindications to implant or bone surgery. It is imperative to systematically refer to the instructions for use provided by Jeil Medical Corp. to know all the precautions for use and the specific limitations of the equipment.

What are the maintenance and durability precautions?

As a non-resorbable surgical instrument, the ROGFIXE screwdriver handle requires a rigorous cleaning, disinfection, and sterilization protocol between each patient. To guarantee the longevity of this Jeil Medical instrument, appropriate cleaning solutions that do not alter the constituent materials should be used. The practitioner must check the integrity of the handle and the insert fixation mechanism before each intervention. Careful handling avoids any deformation that could harm the precision of the screwing. For any information regarding recommended sterilization cycles, consulting the technical manual from the manufacturer Jeil Medical Corp. is indispensable.

Who is the manufacturer and what standards are respected?

The ROGFIXE screwdriver handle (111-010) is officially manufactured by Jeil Medical Corp., a globally recognized player in the field of osteosynthesis and surgical instrumentation. Regarding specific certifications, the CE marking and regulatory class are not specified in the current source data. However, Jeil Medical products are designed according to high quality standards to meet the needs of specialized surgeons. To obtain precise details on regulatory compliance, ISO certificates, or the CE marking in force for this specific model, it is recommended to contact Delynov directly or consult the official technical documentation of the manufacturer.

State of the art

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