Mini Emergency Self Tapping Non-Locking Purple OD - 2.3 L - 8 - JEIL Medical

What is the Mini Emergency Self Tapping Non-Locking Purple OD - 2.3 L - 8 - JEIL Medical?

The Mini Emergency Self Tapping Non-Locking Purple OD - 2.3 L - 8 is a device designed by Jeil Medical for guided bone regeneration (GBR) procedures. This specific component, identified under reference 241.012308, is distinguished by its self-tapping design (Self Tapping) and its non-locked structure (Non-Locking). With an outer diameter of 2.3 and a length of 8, this purple-colored (Purple) device is intended for use by qualified dental surgeons and implantologists. Its design by Jeil Medical Corp. ensures precise integration into surgical bone fixation protocols where primary stability is sought without a complex locking mechanism.

What are the clinical indications for this Jeil Medical device?

This Mini Emergency device from Jeil Medical is primarily indicated for guided bone regeneration (GBR) surgeries and maxillofacial or oral reconstruction. Its self-tapping nature allows for easier insertion into bone tissues when fixing membranes or bone blocks. It is particularly useful in emergency situations or during surgical readjustments requiring reliable fixation with a diameter of 2.3. The use of this Jeil Medical product must be strictly reserved for healthcare professionals trained in implant and bone surgery techniques, thus ensuring handling in accordance with the patient's clinical needs.

What are the technical characteristics of product 241.012308?

The product referenced 241.012308 features precise technical specifications to meet the requirements of oral surgery. It has an outer diameter (OD) of 2.3 and a length (L) of 8. Its 'Self Tapping' nature means it is capable of creating its own thread during insertion, which optimizes operative time and initial mechanical hold. As a 'Non-Locking' model, it offers application flexibility in setups that do not require rigid locking between components. The purple (Purple) finish allows for quick visual identification during surgery, thereby facilitating the practitioner's work within the technical tray.

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

The use of the Mini Emergency Self Tapping from Jeil Medical is contraindicated in patients with uncontrolled systemic pathologies that could compromise bone healing or device integration. Any known allergy to the constituent materials of the device constitutes a major contraindication. It should not be used in sites with active infection or insufficient bone quantity to ensure the stability of the 2.3 diameter. Practitioners must evaluate risks related to smoking, unbalanced diabetes, or local irradiation before any intervention. It is imperative to refer to the technical instructions from the manufacturer Jeil Medical Corp. for the exhaustive list of contraindications.

What are the precautions for use and handling?

When handling the Jeil Medical device, it is essential to scrupulously respect the sterility protocols specific to operating rooms. The practitioner must ensure the use of instrumentation adapted to the 2.3 diameter and 8 length to avoid any material fracture or damage to the surrounding bone. Although this device is self-tapping, excessive pressure during insertion must be avoided to preserve the integrity of the bone thread. As a non-locked device, particular attention must be paid to the final stability of the assembly. Rigorous post-operative follow-up is necessary to monitor clinical progress and ensure the absence of inflammatory or mechanical complications.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., a recognized company in the medical device sector for oral and maxillofacial surgery. The product is distributed under the Jeil Medical brand. Regarding specific certifications, such as the regulatory class or CE marking, information is not specified in the current source data. Practitioners are invited to consult the product labeling as well as the technical documentation provided by Jeil Medical to verify current regulatory compliance and maintenance instructions. Product traceability is ensured by the reference code 241.012308.

State of the art

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