Cogswell Elevator B with Handle Number 510 - Hu-Friedy - Delynov

What is the Cogswell #B elevator handle #510?

The Cogswell #B elevator with #510 handle is a manual instrument developed by the manufacturer Hu-Friedy, intended for the practice of oral surgery and implantology. This device consists of a working part specific to the Cogswell #B model and an ergonomic handle referenced under number 510. This tool is designed to assist practitioners during dental luxation phases. As a product of the Hu-Friedy brand, it benefits from the expertise of a recognized manufacturer in the field of surgical instrumentation. This medical device is classified as Class I according to current regulations, guaranteeing its adequacy with safety requirements for non-invasive or minimally invasive interventions in dental offices.

What are the clinical indications for this cogswell dental elevator?

The use of this cogswell dental elevator is primarily indicated for simple or complex dental extractions. Its clinical role is to facilitate the separation of the tooth from its socket by breaking the fibers of the periodontal ligament. It is particularly useful during the initial stages of avulsion, allowing for the creation of sufficient space for the subsequent insertion of forceps. Dental surgeons and implantologists use this instrument during alveolar surgeries to mobilize roots or impacted teeth. The use of this instrument is strictly reserved for qualified healthcare professionals, in accordance with the directives provided by Hu-Friedy Mfg. Co., LLC, to ensure precise and safe handling during operative protocols.

What are the technical characteristics of this Hu-Friedy instrument?

The Cogswell #B elevator is distinguished by the configuration of its active part, optimized for force transmission during luxation. The #510 handle equipped on this instrument is specifically designed to offer a stable grip, essential for controlling the surgical gesture. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets Class I manufacturing standards. Although specific details on material composition are not provided in the raw technical documentation, the overall design aims to meet the mechanical stresses encountered in oral surgery. Each component is adjusted to guarantee the integrity of the tool during repeated use in a clinical setting, subject to compliance with the sterilization and maintenance protocols recommended by the manufacturer.

What are the contraindications for the use of this instrument?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not exhaustively listed beyond general use warnings. However, the use of this instrument is strictly reserved for trained healthcare professionals. It must not be used for applications other than those intended in dental and oral surgery. An implicit contraindication lies in use by unqualified personnel or in clinical situations where the integrity of the alveolar bone or adjacent structures does not allow the application of leverage force without risk of fracture. It is imperative to read the instructions carefully before use to identify any additional restrictions related to the patient's specific clinical condition.

What are the precautions for use and maintenance?

To ensure the longevity and safety of the Cogswell #B elevator, several precautions must be observed. As a Class I device intended for reuse, it must undergo a complete cycle of cleaning, disinfection, and sterilization between each patient. Professionals must inspect the instrument before each intervention to detect any signs of wear or deformation of the Cogswell #B tip or the #510 handle. Inappropriate handling, such as excessive twisting, could compromise the effectiveness of the instrument or cause damage to periodontal tissues. Hu-Friedy emphasizes the importance of strictly following the reprocessing instructions provided by the manufacturer to maintain the technical performance and microbiological safety of the device within the dental office.

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. This medical device is listed under Class I, which corresponds to products presenting a low degree of risk according to the regulatory classification of medical devices. The Hu-Friedy brand is recognized worldwide for the quality of its surgical instruments. Compliance with manufacturing standards ensures that the elevator meets essential safety and performance requirements. Practitioners wishing to purchase a high-precision dental elevator can refer to the manufacturer's technical documentation to ensure the product's compliance with current clinical protocols. The Class I designation confirms that the instrument follows the conformity assessment procedures required for its placement on the market.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.