Mid L Plate(R) 100° Long Silver t - 0.6 4Holes
The Mid L Plate100° Long Silver t - 0.6 4Holes (242.23LR04) is a medical device manufactured by le fabricant.
- Manufacturer: le fabricant.
- Reference: 242.23LR04.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Mid L Plate(R) 100° Long Silver t - 0.6 4Holes?
The Mid L Plate(R) 100° Long Silver t - 0.6 4Holes, marketed by the brand Marque, is a specific osteosynthesis device. It is a dental surgery L-plate featuring a 100-degree angulation. Its structure includes 4 fixation holes, allowing for rigid immobilization of bone segments. This 'Long Silver' model is distinguished by its dimensions and 't' geometry with a thickness of 0.6, optimizing its integration during oral and maxillofacial surgery interventions. This product is developed by the official manufacturer to meet mechanical stability requirements in complex clinical environments.
What are the clinical indications?
This angled titanium plate is indicated for the maintenance and fixation of bone grafts or fractures in the maxillofacial sector. In oral and implant surgery, it is used to stabilize osteotomies or during advanced bone reconstructions where a 100° angled osteosynthesis plate is necessary to match the patient's morphology. The 4-hole configuration offers several anchoring points, ensuring distribution of compression forces. Practitioners use this device from the brand Marque to guarantee optimal bone healing by preventing micromovements of stabilized fragments during the consolidation phase.
What are the technical characteristics of reference 242.23LR04?
The technical reference 242.23LR04 corresponds to a specific model in the Marque range. Its specifications include an 'L' shape with a 100° angulation, an extended length (Long), and a 'Silver t - 0.6' profile. It is equipped with 4 fixation holes for osteosynthesis screws. The technical design aims to offer a low profile to minimize irritation of surrounding soft tissues while maintaining sufficient mechanical strength for internal fixation applications. Every detail, from hole spacing to the curvature of the plate, is designed by the manufacturer to facilitate surgical implementation.
What are the contraindications for use?
Contraindications for the use of this plate include clinical situations where the bone stock is insufficient to allow stable screw fixation. An active infection at the surgical site also constitutes a major contraindication. As with any metallic implant from the brand Marque, known hypersensitivity to the device's constituent metals must be verified before the intervention. It is the surgeon's responsibility to evaluate the patient's systemic risk factors, such as vascularization disorders or uncontrolled metabolic bone pathologies, which could compromise the success of the osteosynthesis.
What are the precautions related to this non-resorbable device?
The Mid L Plate(R) 100° Long Silver t - 0.6 4Holes is a non-resorbable device. It is designed to remain in place throughout the duration of bone consolidation. Precautions for use include careful handling to avoid scratching or excessively deforming the plate, which could alter its mechanical properties or corrosion resistance. The practitioner must ensure the plate is perfectly applied against the bone and that screws are inserted according to the appropriate axis. Removal of the plate after complete consolidation depends on the clinical protocol chosen by the surgeon and the specific needs of the patient.
Who is the manufacturer and which standards are respected?
The device is produced by the official manufacturer and distributed under the brand Marque. As CONSO category equipment intended for surgical implantation, it is manufactured according to rigorous control processes to guarantee its biocompatibility and reliability. To obtain detailed information on the regulatory class, CE marking, or specific ISO certifications for this reference 242.23LR04, it is imperative to refer to the product labeling and the instructions for use provided by the manufacturer. Compliance with sterilization and placement protocols is essential to guarantee clinical use conformity.
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