Mid L Plate(R) 90° Regular Silver t - 0.6 4Holes - JEIL Medical

What is the Mid L Plate(R) 90° Regular Silver t - 0.6 4Holes?

The Mid L Plate(R) 90° Regular Silver t - 0.6 4Holes is an osteosynthesis device developed by Jeil Medical. It is an l-shaped surgical plate featuring a 90-degree angle, specifically designed for maxillofacial interventions. This model is part of the manufacturer's Regular Silver range and is characterized by a thickness of 0.6 mm and a 4-hole (4Holes) configuration. Its structure is optimized to provide mechanical stability during the fixation of bone fragments while respecting the patient's anatomy thanks to its specific profile.

What are the clinical indications for this l-shaped osteosynthesis plate?

This maxillofacial titanium plate is primarily indicated in orthognathic surgery protocols, facial trauma, and bone reconstruction. As an l-shaped osteosynthesis plate, it is used by oral and maxillofacial surgeons to ensure the maintenance and compression of bone segments after an osteotomy or fracture. Its 90-degree L-shape is particularly suited to areas requiring multidirectional anchoring where a straight plate would not allow for optimal stability of the fracture or cut sites.

What are the technical specifications of model 242.20LR04?

The technical reference 242.20LR04 corresponds to a plate from the Jeil Medical brand featuring precise specifications for specialized surgery. It has a thickness of 0.6 mm, providing a balance between malleability for anatomical adaptation and rigidity for containment. It features 4 holes allowing for the passage of compatible osteosynthesis screws. Its 'Regular Silver' designation and 'Mid L Plate(R) 90°' geometry confirm its use in the intermediate segments of the face where assembly precision is critical for clinical success.

What are the contraindications for the use of this device?

Contraindications for the use of the Jeil Medical Mid L Plate(R) include clinical situations where bone quality is insufficient to guarantee screw anchoring, such as in cases of severe osteoporosis or active infections at the surgical site. Furthermore, any known allergy to the metallic components of the device constitutes an absolute contraindication. The practitioner must also evaluate risks in patients with vascularization disorders or systemic pathologies that could compromise bone healing and the integration of the osteosynthesis material.

What are the precautions related to the non-resorbable nature of the device?

As a non-resorbable metallic device, this l-shaped osteosynthesis plate is intended to remain in place permanently or to be removed during a second intervention once bone consolidation is achieved. Precautions include adequate mucosal coverage to avoid any exposure of the material, which could lead to infectious complications. The surgeon must ensure that the plate is perfectly fitted to the bone surface to minimize tension on the surrounding soft tissues and prevent postoperative mechanical irritation phenomena.

Who is the manufacturer and what standards are met?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of implants and instruments for maxillofacial surgery. Although detailed regulatory specifications such as the exact class or notified body number are not specified in the current source data, Jeil Medical produces its devices according to rigorous quality standards. It is imperative for the healthcare professional to systematically refer to the instructions for use and the product labeling (reference 242.20LR04) to verify current certifications and recommended sterilization protocols.

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