Mid Self Drilling Green OD Screw - 1.6 L - 6 - JEIL Medical (241.021606) - Delynov

What is the Vis Mid Self Drilling Green OD - 1.6 L - 6 - JEIL Medical?

The Vis Mid Self Drilling Green OD is a bone fixation device designed by Jeil Medical for Guided Bone Regeneration (GBR) procedures. This specific model, referenced under code 241.021606 at Delynov, features a diameter of 1.6 and a length of 6. Its self-drilling design allows for direct insertion into the bone tissue without the need for systematic pre-drilling, thus optimizing operative time during oral and implant surgery procedures. Its distinctive green color facilitates visual identification within the surgical field.

What are the clinical indications for this Jeil Medical screw?

This screw is primarily indicated in reconstructive surgery and Guided Bone Regeneration (GBR) protocols. It is used by dental surgeons and implantologists to stabilize barrier membranes or fix bone grafts (bone) during alveolar ridge augmentation. Thanks to its self-drilling technology, it ensures rigid and stable fixation, a sine qua non condition for successful osseointegration and optimal tissue regeneration in areas presenting bone deficits.

What are the technical characteristics of reference 241.021606?

The Mid Self Drilling screw from Jeil Medical is characterized by precise dimensions: a diameter of 1.6 and a length of 6. Its structure is optimized for effective penetration into the cortical bone thanks to its self-drilling tip. This device belongs to the range of fixation solutions for GBR developed by Jeil Medical Corp. The technical design aims to offer high primary stability while minimizing bone trauma during placement, thus meeting the requirements of surgeons specialized in implantology.

What are the contraindications for the use of this fixation device?

The use of the Mid Self Drilling screw is contraindicated in situations where the quality or quantity of residual bone is insufficient to guarantee primary stability of the device. It should not be used in patients presenting general contraindications to oral surgery, such as uncontrolled coagulation disorders or severe metabolic bone pathologies. It is imperative that the practitioner evaluates the risks of local infections or active inflammation at the surgical site before any placement of Jeil Medical fixation material.

What are the precautions for use for a non-resorbable screw?

As a metallic fixation device intended for GBR, this screw is non-resorbable. It must be handled with specific instruments compatible with the Jeil Medical system to avoid any contamination or damage to the screw thread. The surgeon must take care not to apply excessive tightening torque during insertion to prevent any fracture of the device or necrosis of the surrounding bone. Removal of the screw must be planned once bone consolidation or stabilization of the graft is achieved, in accordance with the established clinical protocol.

Who is the manufacturer and what are the recommendations for use?

The official manufacturer of this device is Jeil Medical Corp., a recognized company in the field of fixation systems for maxillofacial and dental surgery. For any information concerning the standards met, the regulatory class, or specific certifications, healthcare professionals are invited to systematically consult the user manual and instructions provided by the manufacturer with the product. As an expert in fixation solutions (bone fixation), Jeil Medical advocates strict use by practitioners trained in oral surgery and bone regeneration techniques.

State of the art

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