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

What is the Mid Self Drilling Green OD - 1.6 L - 6 screw?

The Mid Self Drilling Green OD - 1.6 L - 6 screw is a miniaturized fixation device designed by Jeil Medical for oral surgery. This model is distinguished by its self-drilling tip which allows direct penetration into the bone cortex without the need for a pilot drill. Its structure is optimized for guided bone regeneration, offering the primary stability essential for maintaining filling materials under the membrane. Its technical reference 241.021606 corresponds to a diameter of 1.6 mm and a length of 6 mm. The green color finish allows the practitioner to quickly identify it among the different diameters of the Jeil Medical Corp range during the intervention.

What are the clinical indications for this Jeil Medical screw?

This titanium self-drilling screw is primarily indicated in pre-implant and periodontal bone reconstruction procedures. It is used by dental surgeons and implantologists to fix protective membranes (resorbable or non-resorbable) or titanium meshes. Its use is common during horizontal or vertical ridge augmentations, where strict immobilization of the barrier device is crucial for the success of osseointegration and the prevention of connective tissue invasion. Its surgical self-drilling design makes it particularly effective in areas where access is limited, simplifying the technical procedure while guaranteeing solid anchorage in the recipient bone.

What are the technical characteristics of reference 241.021606?

The dental self-drilling screw referenced 241.021606 features precise specifications to meet the requirements of modern implantology. It has a diameter of 1.6 mm and a useful length of 6 mm, offering an ideal compromise between fineness and mechanical strength. Jeil Medical's 'Self Drilling' technology integrates a screw thread and a sharp point capable of tapping the bone simultaneously with insertion. This characteristic reduces operating time and limits thermal heating related to drilling. Its head is designed for a secure grip with the brand's screwdrivers, avoiding risks of accidental disconnection during placement at the surgical site.

What are the contraindications for the use of this device?

Although specific manufacturer data are not detailed here, classic contraindications for this type of titanium self-drilling screw include uncontrolled systemic pathologies affecting bone metabolism or healing. Insufficient oral hygiene or an active infection at the surgical site constitute major contraindications. It is also imperative to verify the absence of known allergies to the metals constituting the device. The practitioner must evaluate the patient's bone density; excessively dense bone or, conversely, too spongy bone may require an adaptation of the fixation protocol. It is recommended to systematically refer to the instructions for use provided by Jeil Medical Corp.

What precautions should be taken during placement and removal?

The use of the titanium self-drilling screw requires precise handling with dedicated Jeil Medical instrumentation. During placement, the practitioner must apply controlled axial pressure to engage the self-drilling tip without deviating from the desired axis. As a non-resorbable device, this screw is intended to be removed after the bone consolidation phase, generally during implant placement or the surgical re-entry phase. Care should be taken to ensure that the screw head is not covered by excessive bone growth, which could complicate its removal. Particular attention must be paid to the stability of the fixed membrane to avoid any micro-movement detrimental to regeneration.

Who is the manufacturer and what standards are respected?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and surgical instrumentation. Although specific details on the CE marking or regulatory class are not explicitly mentioned in the current source data, Jeil Medical products are designed according to rigorous quality standards for use in a sterile environment. As a distributor, Delynov ensures the traceability of these guided bone regeneration devices. For any information relating to conformity certifications, applied ISO standards, or regulatory marking details (MDR), healthcare professionals are invited to consult the technical documentation and the instruction manual accompanying the product.

State of the art

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