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

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

The Mid Self Drilling Green OD Screw is an osteosynthesis device designed by Jeil Medical. This specific hardware, identified under reference 241.021606, belongs to the category of products intended for Guided Bone Regeneration (GBR). This self-drilling screw features a diameter of 1.6 and a length of 6. It is designed to facilitate surgical procedures by eliminating the pre-drilling step, thus allowing stable and precise fixation of membranes or bone blocks during alveolar reconstruction interventions.

What are the clinical indications for this Jeil Medical screw?

This screw from the Jeil Medical range is primarily indicated in oral surgery, implantology, and maxillofacial surgery protocols requiring graft or barrier stabilization. It is used to fix bone regeneration devices during ridge augmentation procedures or bone defect filling. Its self-drilling design is particularly suitable for maintaining adequate compression and ensuring the immobilization necessary for successful bone integration in areas of low or medium density.

What are the technical specifications of reference 241.021606?

The Mid Self Drilling Green OD screw from Jeil Medical is distinguished by its precise technical specifications. It has a diameter of 1.6 and a length of 6. Its self-drilling nature allows direct insertion into the bone without the need for a pilot drill, which reduces operative time and limits thermal heating of the tissues. The green color (Green OD) allows for rapid visual identification when selecting hardware on the surgical tray. This device is a key component of fixation systems for GBR, guaranteeing optimal mechanical hold.

What are the contraindications for the use of this device?

The use of the Jeil Medical Mid Self Drilling screw is contraindicated in patients with uncontrolled systemic pathologies affecting bone metabolism or healing. It should not be used in areas with active infection or insufficient residual bone quantity to ensure primary stability of the device. The practitioner must assess the risks related to poor bone quality that could compromise the screw's hold. It is imperative to refer to the manufacturer's technical instructions for the exhaustive list of contraindications related to this osteosynthesis hardware.

What are the precautions for use and removal for this non-resorbable screw?

As a metallic device intended for bone fixation, this screw is non-resorbable. It must remain in place throughout the duration of the healing and consolidation phase of the graft or membrane. The practitioner must ensure correct axis insertion to avoid any hardware fracture or damage to adjacent anatomical structures (nerves, tooth roots). Once the regeneration objective is achieved, removal must be performed with specific Jeil Medical brand instrumentation to guarantee secure removal without altering the newly formed bone.

Who is the manufacturer of this device and what is the regulatory information?

The official manufacturer of this device is Jeil Medical Corp., an internationally recognized company in the field of osteosynthesis. This product, distributed by Delynov, is specifically developed to meet the requirements of dental and maxillofacial surgeons. For any information concerning the regulatory class, CE marking, or certification standards specific to reference 241.021606, healthcare professionals are invited to consult the product labeling and technical documentation provided by Jeil Medical to ensure use in compliance with current safety requirements.

State of the art

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