Elevator number 46, bur number 510, upper molars - Hu-Friedy - Delynov

What is the Hu-Friedy #46 elevator with #510 handle?

The #46 elevator with #510 handle is a manual instrument developed by the manufacturer Hu-Friedy, a recognized leader in the field of surgical instrumentation. This device is specifically configured for interventions on upper molars. It consists of a working part adapted to the anatomy of the posterior maxillary areas and an ergonomic handle referenced under number 510. This product belongs to the category of consumables (CONSO) for dental and oral surgery. As a Class I medical device, it meets standard regulatory requirements for non-invasive or invasive instruments for temporary use, thus guaranteeing compliance for use in dental offices or hospital environments by qualified practitioners.

What are the clinical indications for this instrument?

This elevator is indicated for simple or complex extraction procedures involving upper molars. Its primary role is to induce the rupture of periodontal ligament fibers through a controlled lever or rotation movement. It is used by dental surgeons and implantologists to luxate the tooth from its socket, thereby facilitating its final removal. The use of this Hu-Friedy instrument is particularly recommended when access to upper molars requires precise angulation. It can also be used in the mobilization of residual roots or during pre-implant surgeries requiring alveolar clearance. In accordance with the guidelines of the manufacturer Hu-Friedy Mfg. Co., LLC, this instrument is exclusively reserved for healthcare professionals trained in oral surgery techniques.

What are the technical characteristics of the #46 elevator?

The #46 elevator is distinguished by its active part specifically oriented for the upper molar sector. The associated #510 handle offers a grip adapted to the torsional forces required during dental luxation. Although the exact material composition is not specified in the provided technical documentation, the manufacturing standards of Hu-Friedy Mfg. Co., LLC ensure quality adapted to the constraints of oral surgery. As a Class I device, it is designed to withstand standard sterilization cycles in the office, subject to following the instructions in the manual. Its geometry is designed to minimize the risk of alveolar fracture while maximizing the efficiency of force transfer during the elevation of maxillary molars.

What are the contraindications for the use of this device?

Specific contraindications are not exhaustively listed in the manufacturer's raw data, beyond general warnings. However, the use of this instrument is strictly reserved for healthcare professionals. It must not be used outside of its intended use, namely the elevation of upper molars. Standard clinical contraindications in oral surgery apply, such as use on weakened bone structures without adequate precaution or on patients presenting general contraindications to tooth extraction. It is imperative to carefully read the manual provided by Hu-Friedy before any use to identify any restrictions related to the patient's condition or the surgical technique employed.

What are the precautions for use and maintenance?

Like any Class I surgical instrument, the Hu-Friedy #46 elevator requires rigorous handling. Before the first use and after each intervention, the device must be cleaned, disinfected, and sterilized in accordance with current protocols and the instructions of the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA. The practitioner must inspect the instrument before use to detect any sign of wear or deformation that could compromise patient safety or the effectiveness of the surgical procedure. Particular attention should be paid to the #510 handle and the active tip to ensure their integrity. Compliance with the recommended sterilization cycles is essential to maintain the functional properties of the steel and guarantee asepsis during molar extraction surgeries.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a globally recognized manufacturer for the quality of its dental instrumentation. This medical device is classified as Class I according to current regulations. Although specific CE marking is not mentioned in the source data, the product complies with American and international manufacturing standards imposed on medical devices in this category. The indications and warnings provided by Hu-Friedy emphasize that the use of this elevator is strictly reserved for healthcare professionals. Practitioners are invited to systematically consult the instructions for use to ensure practice consistent with safety and clinical efficacy requirements.

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