Mesh plate cutter - JEIL Medical (114-007) - Delynov

What is the Jeil Medical mesh plate cutter?

The mesh plate cutter, referenced under code 114-007 at Delynov, is a specialized surgical instrument designed by Jeil Medical Corp. This tool is specifically developed for the manipulation and precise cutting of mesh plates used during bone reconstruction or stabilization procedures. As an accessory in the Jeil Medical range, it meets the needs of practitioners requiring reliable instrumentation to adapt fixation devices to the anatomical specificities of each patient. Its ergonomic design allows for an optimal grip for a clean sectioning of mesh structures, thus facilitating the surgeon's work during critical phases of the intervention.

What are the clinical indications for this instrument?

The Jeil Medical mesh plate cutter is indicated for use during oral, maxillofacial, or implant surgeries requiring the adjustment of reinforcement or maintenance plates. Its primary use lies in cutting mesh-type devices to conform them perfectly to the operative site. This instrument is essential for dental surgeons and implantologists performing guided bone regeneration procedures or complex reconstructions where precise adaptation of fixation material is crucial for clinical success and post-operative patient comfort. It allows for sectioning meshes without deforming the overall structure of the material.

What are the technical characteristics of model 114-007?

The Jeil Medical model 114-007 is distinguished by its robustness and cutting precision. Although detailed composition specifications are not explicitly mentioned, this instrument is designed to withstand the mechanical stresses associated with sectioning metal or synthetic mesh plates. Its geometry is studied to provide an effective lever arm, reducing the effort required during manipulation while ensuring maximum visibility of the cutting area. Reference 114-007 ensures precise traceability within the Jeil Medical instrumentation range distributed by Delynov, thus guaranteeing the acquisition of a tool specifically dedicated to this technical use.

What are the contraindications for the use of this plate cutter?

The use of the Jeil Medical mesh plate cutter is contraindicated for sectioning materials whose hardness or thickness exceeds the nominal capacities of the instrument, such as solid fixation plates or large diameter screws, which could damage the cutting jaws. Generally, this instrument must not be used outside of its intended use in specialized surgery. It is the practitioner's responsibility to check the integrity of the tool before each intervention. Any use on structures incompatible with the blade's fineness can lead to premature wear or breakage of the instrument, compromising the safety of the surgical act.

What are the maintenance and handling precautions?

To guarantee the longevity of the Jeil Medical mesh plate cutter, it is imperative to follow the cleaning, disinfection, and sterilization protocols recommended for reusable surgical instrumentation. After each use, the instrument must be thoroughly cleaned to remove any organic residue before the sterilization cycle. It is advised to regularly inspect blade alignment and the absence of corrosion. Careful handling is required to avoid distorting the cutting mechanism. Compliance with these precautions ensures constant performance and the sectioning precision essential when adjusting mesh plates at the surgical site.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is Jeil Medical Corp., a company globally recognized for its expertise in the field of fixation devices and surgical instrumentation. Regarding specific certifications such as CE marking or regulatory class, this information is not specified in the current technical documentation. It is therefore strongly recommended that healthcare professionals systematically consult the instructions for use provided by Jeil Medical and the product labeling to verify compliance with current standards and obtain details relating to sterilization protocols validated by the manufacturer before any clinical implementation.

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