Mid Straight Long Silver t - 0.6 4Holes - JEIL Medical

What is the Mid Straight Long Silver t - 0.6 4Holes - Jeil Medical plate?

The Mid Straight Long Silver t - 0.6 4Holes plate, referenced under code 242.21ST04 by Jeil Medical, is a metallic osteosynthesis device. This straight surgery plate features a 4-hole configuration, designed to provide a stable fixation interface between bone segments. Its rectilinear and elongated structure is specifically adapted to the needs of reconstructive surgery. As a straight titanium plate, it is selected for its mechanical properties and compatibility with the physiological environment during bone healing phases.

What are the clinical indications for this osteosynthesis plate?

This dental and maxillofacial osteosynthesis plate is indicated for fracture stabilization, corrective osteotomies, and bone reconstruction procedures. It is used by surgeons to ensure rigid maintenance of bone fragments, thereby promoting primary union. Its straight format makes it particularly useful in anatomical areas requiring simple linear contention. It is part of trauma or orthognathic surgery protocols where a titanium surgery plate is required to support mechanical loads during the consolidation period.

What are the technical characteristics of reference 242.21ST04?

Reference 242.21ST04 from Jeil Medical is characterized by a 0.6 profile, indicating the thickness or technical gauge of the device. It has 4 fixation holes, allowing for the passage of osteosynthesis screws to securely anchor the plate to the bone. Its 'Mid Straight Long' designation confirms a straight morphology and an extended length compared to standard models, offering a larger contact surface and multiple anchoring points. This straight osteosynthesis plate is designed to meet the precision requirements of complex surgical interventions.

What are the contraindications for the use of this device?

The use of this plate is contraindicated in patients with a known hypersensitivity to the metals constituting the device, particularly if components such as titanium are involved. It must not be used in situations of active infection at the operative site or in the presence of insufficient bone stock to guarantee stable screw anchoring. Metabolic pathologies severely interfering with bone healing may also constitute a contraindication. It is the surgeon's responsibility to evaluate the benefit-risk ratio based on the patient's systemic status.

What precautions are associated with the non-resorbable nature of the product?

This metal plate is a non-resorbable device, meaning it does not degrade in the body through hydrolysis or enzymatic resorption. It is intended to remain in place permanently to ensure structural stability, unless a clinical decision justifies its removal after complete consolidation (generally in case of discomfort or complication). Practitioners must ensure adequate soft tissue coverage to avoid any exposure of the hardware. Regular post-operative follow-up is essential to monitor for the absence of migration or adverse tissue reactions.

Who is the manufacturer Jeil Medical and what standards are respected?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of fixation systems for oral and maxillofacial surgery. Although the specific regulatory class and CE marking are not detailed in the source data for this precise reference, Jeil Medical generally produces its devices according to rigorous quality standards. Healthcare professionals are invited to consult the technical instructions attached to the product or the labeling of reference 242.21ST04 to verify current certifications and recommended sterilization protocols before any implantation.

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