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Screwdriver for ROGFIXE micro-screws (111-010 113-MD-101) - Jeil Medical - Delynov

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The Tournevis pour micro-vis ROGFIXE (111-010 113-MD-101) - Jeil Medical is a medical device manufactured by Jeil Medical Corp..

  • Manufacturer: Jeil Medical Corp..
  • Reserved for healthcare professionals. Read instructions carefully before use.

237.20 € 237.2 EUR 237.20 € Tax Included 324.96 €

237.20 € Tax Included 324.96 €

(0.00 € / Units)

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GBR

What is the ROGFIXE Jeil Medical micro-screw screwdriver?

The ROGFIXE micro-screw screwdriver is a precision surgical instrument designed by Jeil Medical. This device, referenced under codes 111-010 and 113-MD-101, is specifically developed for the handling and insertion of micro-screws during Guided Bone Regeneration (GBR) procedures. It belongs to the specialized range of Jeil Medical Corp., offering practitioners an ergonomic tool adapted to the requirements of oral and implant surgery. Its design aims to ensure a stable grip and optimal control during the placement of bone fixation systems.

What are the clinical indications for the ROGFIXE screwdriver?

This screwdriver is indicated for oral, maxillofacial, and implant surgery procedures requiring the use of fixation micro-screws. It is primarily used within Guided Bone Regeneration (GBR) protocols to stabilize membranes or fix bone blocks. The use of this Jeil Medical instrument is reserved for healthcare professionals trained in bone reconstruction techniques, ensuring precise application of micro-screws in complex surgical sites where space is often restricted.

What are the technical characteristics of this device?

The ROGFIXE screwdriver, identified by references 111-010 and 113-MD-101, is characterized by a connection interface compatible with the micro-screws of the Jeil Medical range. Although material specifications are not detailed in the source data, this instrument is designed to meet the mechanical constraints of bone surgery. Its structure allows for efficient transmission of tightening torque while maintaining adequate visibility of the operative field. It integrates perfectly into the Delynov GBR catalog to support dental surgeons in their graft stabilization procedures.

What are the contraindications for the use of this instrument?

Contraindications for the use of the ROGFIXE micro-screw screwdriver include any clinical situation where the use of fixation micro-screws is itself contraindicated, such as insufficient bone density or serious systemic pathologies affecting healing. It must not be used with non-compatible screws whose diameter or drive does not correspond to references 111-010 and 113-MD-101. Practitioners must refer to the technical instructions from the manufacturer Jeil Medical Corp. to identify any specific restrictions related to the patient's health status or the surgical technique employed.

What are the precautions for use and maintenance?

Like any bone surgery instrument, the ROGFIXE screwdriver requires rigorous handling to avoid any deformation of the tip or the drive. Before each procedure, it is imperative to check the integrity of the instrument and its perfect compatibility with the selected micro-screws. After use, the device must follow a cleaning and sterilization protocol in accordance with the recommendations of the manufacturer Jeil Medical. Particular attention must be paid to maintaining the cleanliness of the connection area to guarantee the durability of technical performance during the screwing phases in GBR surgery.

Who is the manufacturer and what is the regulatory information?

The ROGFIXE micro-screw screwdriver is manufactured by Jeil Medical Corp., a recognized player in the field of medical devices for osteosynthesis and oral surgery. For any information relating to the regulatory class, CE marking, or specific compliance standards, it is essential to consult the original labeling and the instructions for use provided by Jeil Medical with the product. As a specialized distributor, Delynov ensures that these instruments intended for implantology professionals meet the technical requirements necessary for performing bone regeneration procedures.


State of the art

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