Micro Straight Regular Gold t - 0.5 2Holes - JEIL Medical

What is the Micro Straight Regular Gold t micro plate?

The Micro Straight Regular Gold t, referenced under code 242.10ST02, is a bone fixation device designed by Jeil Medical. It is a straight surgical micro plate belonging to the Regular Gold t range. Its structure is specifically developed to provide a maintenance interface between two bone segments. This type of equipment is commonly used in maxillofacial surgery to ensure primary stability during bone healing phases. Its compact design allows for discrete integration under soft tissues while maintaining the mechanical properties necessary for osteosynthesis.

What are the clinical indications for this Jeil Medical device?

This surgical mini plate is indicated for the internal fixation of facial skeleton and cranial bone fractures. It finds its application in orthognathic surgery procedures, the reconstruction of minor facial traumas, or bone grafts requiring stabilization by a titanium osteosynthesis plate. In oral surgery, it may be used to maintain bone blocks or stabilize segments after an osteotomy. The choice of this 2-hole (2Holes) model is particularly suitable for areas where space is restricted and where a short linear fixation is sufficient to ensure fragment cohesion.

What are the technical characteristics of reference 242.10ST02?

Reference 242.10ST02 corresponds to a straight micro plate from the Regular Gold t series by Jeil Medical. Its main features include a 2-hole (2Holes) configuration with a 0.5 spacing. This specific geometry allows the surgeon to perform precise fixation with minimal bulk. Although detailed material specifications are not explicitly listed, this type of maxillofacial surgery mini plate is traditionally designed to offer optimal biocompatibility and mechanical resistance adapted to the physiological stresses of the facial skeleton.

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

Contraindications for the use of the Jeil Medical micro plate include clinical situations where bone stock is insufficient to guarantee stable anchoring of the fixation screws. It must not be used in cases of active infection at the surgical site or in patients with known allergies to the construction metals of the osteosynthesis devices. Furthermore, insufficient vascularization of the area or severe metabolic disorders affecting bone healing may compromise the success of the implantation. It is the practitioner's responsibility to evaluate the benefit-risk ratio based on the patient's general health status.

What are the precautions for use for this non-resorbable material?

As a metallic osteosynthesis device, this micro plate is non-resorbable. It is intended to remain in place permanently, unless a clinical complication or a specific patient request justifies its removal after complete bone consolidation. Precautions include careful handling to avoid scratching or excessively deforming the plate, which could alter its fatigue resistance. The practitioner must ensure adequate coverage by soft tissues to prevent any postoperative exposure. Regular radiographic follow-up is advised to check the stability of the assembly and the absence of material migration.

Who is the manufacturer and what standards are respected?

The product is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of medical devices for osteosynthesis and maxillofacial surgery. Although specific certifications (regulatory class or CE marking) are not detailed in the current source data, Jeil Medical follows the rigorous manufacturing protocols specific to implantable devices. To obtain precise information on the risk class (generally Class IIb for permanent implants) and the certificates of conformity in force, it is imperative to refer to the technical instruction manual and labeling provided by the manufacturer with product 242.10ST02.

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