Block with Micro Screws and Pins - Jeil Medical (112-082) - Delynov

What is the Jeil Medical micro-screw and pin block (112-082)?

The micro-screw and pin block, referenced under code 112-082, is a storage and organization device designed by Jeil Medical for guided bone regeneration (GBR) procedures. This technical support allows for the centralization and securing of micro-screws and pins required during surgical interventions. Its structure is specifically adapted to facilitate access to bone fixation components, thereby ensuring optimal instrumentation management on the sterile tray. Developed by Jeil Medical Corp., this accessory is an essential element for practitioners seeking to maintain an orderly and efficient working environment during critical phases of membrane stabilization or grafting.

What are the clinical indications for this storage block?

This Jeil Medical storage block is indicated for dental surgeons, implantologists, and maxillofacial surgeons performing guided bone regeneration (GBR) procedures. It is used to organize micro-screws and fixation pins before and during the surgical act. Its use is particularly relevant during alveolar ridge reconstruction surgeries or bone defect filling, where precision and speed of access to fixation systems are paramount. By grouping components from the Jeil Medical brand, this block helps prevent the loss of small surgical elements and facilitates post-operative instrumentation counting.

What are the technical characteristics of the 112-082 block?

The Jeil Medical micro-screw and pin block, bearing technical reference 112-082, is distinguished by its ergonomic design dedicated to precision storage. Although specific dimensions are not detailed, this device is configured to accommodate micro-screws and pins from the Jeil Medical Corp. range. Its configuration allows for rapid identification of different screw diameters or lengths stored, thus optimizing the workflow in oral surgery. The robustness of the materials used for its manufacture ensures durability compatible with the requirements of dental practices specialized in implantology and reconstructive surgery.

What are the contraindications for the use of this device?

There are no direct clinical contraindications related to the use of this storage block as an instrumentation support. However, it must not be used for components that are incompatible with its specific slots to avoid any risk of falling or damage to the micro-screws. Practitioners must ensure that the block is used in accordance with the asepsis protocols in force in the dental practice. As with any surgical accessory, inappropriate handling or use outside the intended framework for organizing Jeil Medical fixation systems could compromise the ergonomics of the procedure.

What are the maintenance and sterilization precautions?

To ensure the longevity of the Jeil Medical micro-screw and pin block (112-082), it is imperative to follow the maintenance recommendations provided by the manufacturer. Before any use, the device must undergo appropriate cleaning and sterilization cycles to maintain a rigorous sterile field. It is advisable to regularly inspect the block to check for the absence of residues or structural degradation that could hinder the correct holding of screws or pins. Particular attention must be paid to drying to avoid any alteration of the storage surfaces, thus ensuring consistent performance during GBR procedures.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., a company recognized worldwide for its expertise in bone fixation solutions in dental and maxillofacial surgery. Regarding regulatory certifications such as CE marking or the specific risk class, this information is not specified in the current technical documentation for reference 112-082. Healthcare professionals are invited to systematically consult the instructions for use and the Jeil Medical product labeling to verify compliance with local and international standards in force before any clinical implementation.

State of the art

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