Self-tapping silver plated screw tap - 1.6 L - 5 - JEIL Medical (241.011605) - Delynov

What is the Jeil Medical silver self-tapping screw (241.011605)?

The silver self-tapping screw OD - 1.6 L - 5 is a precision medical device designed by Jeil Medical Corp. for guided bone regeneration (GBR) procedures. Identified under technical reference 241.011605, this screw is distinguished by its specific design allowing for efficient insertion into bone tissues. As a fixation element, it is intended for dental, oral, and maxillofacial surgery professionals seeking reliable components to stabilize structures during reconstruction protocols. Its silver color allows for rapid visual identification during clinical handling.

What are the clinical indications for this fixation device?

This Jeil Medical device is primarily indicated in oral surgery procedures requiring rigid fixation. Its use is common during guided bone regeneration (GBR) protocols for maintaining membranes or bone blocks. Dental surgeons and implantologists use this self-tapping screw to ensure the primary stability necessary for successful osseointegration or graft consolidation. It meets the requirements of complex surgical environments where screwing precision is crucial for the success of implant or reconstructive treatment.

What are the technical characteristics of the 241.011605 screw?

The Jeil Medical silver self-tapping screw features precise technical specifications to optimize the surgical procedure. According to its designation, it has an outer diameter (OD) of 1.6 mm and a length (L) of 5 mm. Its self-tapping function is a major feature that facilitates the engagement of the screw into the bone, potentially reducing the need for prior tapping in certain bone densities. This technical design aims to offer optimal mechanical stability while minimizing operative trauma during the placement of the fixation hardware.

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

The use of the Jeil Medical screw is contraindicated in patients with uncontrolled systemic pathologies that could affect bone metabolism or healing. Generally, it should not be used in the event of an active infection at the surgical site or in the presence of insufficient bone quantity to guarantee stable anchorage. It is the practitioner's responsibility to evaluate risks related to potential allergies to the device's metallic components. For an exhaustive list of specific contraindications, healthcare professionals must imperatively refer to the technical instructions provided by Jeil Medical Corp.

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

As a metallic fixation device, this screw is non-resorbable. It requires regular clinical monitoring to ensure the absence of post-operative complications. The practitioner must ensure the use of appropriate placement instruments compatible with the screw head to avoid any structural damage during insertion or subsequent removal. Removal of the hardware, if planned in the treatment plan, must be performed once the stabilization or regeneration objectives are achieved, in accordance with standard oral and maxillofacial surgery protocols.

Who is the manufacturer and what is the information regarding standards?

The official manufacturer of this device is Jeil Medical Corp., a recognized player in the field of surgical instrumentation and implants. Regarding regulatory certifications such as the device class, CE marking, or specific ISO standards, the information is not detailed in the current source data. Practitioners are invited to consult the product labeling and technical documentation accompanying reference 241.011605 to verify compliance with current regulatory requirements. Delynov is committed to providing products from specialized manufacturers like Jeil Medical to guarantee the quality of the hardware offered.

State of the art

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