Micro Self Tapping Gold OD - 1.3 L - 8 - JEIL Medical

What is the Micro Self Tapping Gold OD - 1.3 L - 8 from Jeil Medical?

The Micro Self Tapping Gold OD is a high-precision surgical device designed by Jeil Medical for Guided Bone Regeneration (GBR) procedures. This specific model, bearing reference 241.011308, is distinguished by its self-tapping design, facilitating its insertion during operative protocols. With an outer diameter of 1.3 and a length of 8, this material is optimized for the specific needs of dental surgeons and implantologists seeking a reliable solution for the fixation of membranes or bone blocks. Its structure is designed to offer optimal primary stability while respecting the integrity of the surrounding tissues.

What are the clinical indications for this device?

This Jeil Medical device is primarily indicated for oral and implant surgeries requiring rigid fixation. It is used during Guided Bone Regeneration (GBR) procedures to stabilize protective barriers or bone grafts. Its use is particularly relevant for practitioners performing ridge augmentations or complex bone reconstructions where screwing precision is crucial. As a self-tapping screw, it allows for direct placement into the bone, thereby reducing operative time and improving patient comfort during the surgical intervention.

What are the technical characteristics of model 241.011308?

The Micro Self Tapping Gold OD model features precise technical specifications to meet the requirements of micro-surgery. It features a diameter of 1.3 and a length of 8 (1.3 L - 8), dimensions adapted to anatomical areas with low bone volume. The self-tapping technology integrated by Jeil Medical Corp. allows the screw to create its own thread during insertion, ensuring solid and secure anchorage. The 'Gold' finish can facilitate visual identification of the device during placement or during a potential reintervention. Each feature is designed to ensure easy handling with dedicated instrumentation.

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

Although specific contraindication data are not detailed in the provided sources, the use of this type of fixation device in oral surgery should generally be avoided in cases of active infection at the surgical site or uncontrolled systemic pathologies affecting bone healing. Insufficient oral hygiene or inadequate residual bone volume to support the 1.3 diameter may also constitute limits to its use. It is the practitioner's responsibility to evaluate the quality of the recipient site and to consult the technical instructions from the manufacturer Jeil Medical Corp. to validate the suitability of the product with the patient's clinical status.

What precautions should be taken when using this non-resorbable material?

As a metallic device used in GBR, this material is by nature non-resorbable. Precautions for use include rigorous handling with appropriate gripping tools to avoid any contamination or deformation of the thread. The surgeon must ensure that the length of 8 is compatible with the thickness of the available bone to avoid any injury to underlying anatomical structures (nerves, sinuses). After the healing phase or integration of the graft, a second intervention may be necessary for the removal of the device, in accordance with the treatment plan initially established by the implantologist.

Who is the manufacturer and what standards are met by this product?

This device is manufactured by Jeil Medical Corp., a globally recognized player in the field of osteosynthesis and solutions for maxillofacial and dental surgery. The product is distributed by Delynov under technical reference 241.011308. For any information relating to regulatory certifications, such as CE marking, the class of the device, or specific ISO standards met, it is imperative to refer to the product labeling and the technical documentation provided by the manufacturer. Jeil Medical ensures rigorous traceability of its devices to guarantee the safety of healthcare professionals and their patients.

State of the art

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