Micron Screw Block and Mesh Plate - Jeil Medical (112-060) - Delynov

What is the Mesh plate and micro-screw block - Jeil Medical (112-060)?

The Mesh plate and micro-screw block, referenced under code 112-060, is a specialized storage device designed by Jeil Medical Corp. This product is specifically developed for practitioners performing guided bone regeneration (GBR) procedures. It is presented as a titanium micro-screw box structured to methodically house and organize micro-screws as well as Mesh-type plates required for the stabilization of grafts and membranes. Its design allows for ergonomic handling in oral surgery practices, offering a compact and orderly storage solution for all small osteosynthesis components from the Jeil Medical brand.

What are the clinical indications for this device?

This storage block is indicated for all oral and implant surgery procedures requiring the use of miniaturized fixation systems. Its primary use focuses on guided bone regeneration protocols where precise management of micro-screws and Mesh plates is crucial. As an osteosynthesis storage box, it allows for efficient preparation of the surgical tray before the intervention, ensuring that Jeil Medical components are ready to be picked up. It is particularly useful during horizontal or vertical bone augmentations requiring rigid fixation to guarantee the successful integration of the filling material.

What are the technical characteristics of this block?

The micro-screw and Mesh plate block (112-060) is distinguished by its internal configuration adapted to the specific dimensions of Jeil Medical dental micro-screws and Mesh plates. This osteosynthesis screw box is designed to withstand the cleaning and sterilization cycles required in a surgical environment, although exact material specifications should be verified in the manufacturer's technical instructions. Its structure allows for secure retention of components while facilitating their retrieval by the practitioner using an appropriate screwdriver. The internal layout is optimized to minimize footprint while maximizing the visibility of the different screw diameters or lengths stored.

What are the contraindications for the use of this product?

There are no direct medical contraindications related to the use of this storage block as such, as it does not come into permanent contact with the patient. However, the use of the components it contains (screws and plates) is subject to the standard contraindications of implant surgery and osteosynthesis, such as active infections at the surgical site, uncontrolled systemic diseases affecting bone healing, or known allergies to the fixation materials. It is imperative to systematically refer to the instructions for use provided by Jeil Medical Corp for specific restrictions related to the implantable devices associated with this block.

What are the maintenance and use precautions?

As a GBR screw storage box, this device must be maintained according to strict decontamination and sterilization protocols before each clinical use to prevent any risk of cross-contamination. The practitioner must ensure that the block is correctly loaded with the corresponding micro-screws and plates before starting the procedure. It is recommended to periodically check the integrity of the block and its storage slots. Particular attention must be paid to the compatibility of the retrieval instruments with the components housed in the Jeil Medical block to avoid damaging the screw threads or screw heads during handling.

Who is the manufacturer and what standards are met?

The micro-screw and Mesh plate block (112-060) is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis devices for maxillofacial and dental surgery. Although specific certifications (regulatory class or CE marking) are not detailed in the current source data, Jeil Medical products are generally designed to meet strict international quality requirements governing medical devices. For any precise information regarding regulatory compliance, CE marking, or reprocessing instructions, healthcare professionals are invited to consult the official technical documentation and labeling accompanying the product delivered by Delynov.

State of the art

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