Lifter number 23 with handle number 510 - Hu-Friedy - Delynov

What is the elevator #23 handle #510 Hu-Friedy?

The elevator #23 handle #510, designed by the manufacturer Hu-Friedy, is a specialized manual instrument intended for oral and implant surgery. This Class I medical device consists of an active part referenced #23 and an ergonomic handle type #510. It is specifically developed to meet the requirements of practitioners during dental luxation phases. As a product from the Hu-Friedy Mfg. Co., LLC catalog, this instrument benefits from the expertise of a recognized manufacturer in the field of surgical instrumentation. It is exclusively reserved for use by qualified healthcare professionals, ensuring application in accordance with clinical protocols in force in dental practices and hospitals.

What are the clinical indications for this instrument?

The intended use of this Hu-Friedy elevator primarily concerns simple or complex extraction procedures. It is indicated for the mobilization of roots and teeth prior to the use of forceps, allowing for the minimization of the force required for avulsion. In oral surgery, its role is crucial for separating the tooth from its alveolar ligament attachment. The indications provided by Hu-Friedy specify that the instrument must be used in accordance with its destination as a luxation device. It is suitable for routine interventions as well as pre-implant surgeries requiring careful management of the socket. Compliance with the indications and contraindications mentioned by the manufacturer is imperative to ensure patient safety and the effectiveness of the surgical procedure.

What are the technical characteristics of the elevator #23 handle #510?

This Hu-Friedy instrument is distinguished by the combination of the #23 tip and the #510 series handle. Although specific details on the exact composition are not explicitly listed in the source data, the design by Hu-Friedy Mfg. Co., LLC ensures manufacturing that meets Class I medical device standards. The #510 handle is designed to offer a grip adapted to the rotational and leverage movements necessary during elevation. The #23 working part has its own geometry allowing access to interproximal spaces for effective application of force. Each component is designed to withstand the mechanical stresses related to luxation while allowing for sterilization in accordance with hospital hygiene standards.

What are the contraindications for the use of this instrument?

According to the regulatory information provided, contraindications are related to the intended use and warnings from the manufacturer Hu-Friedy. Although no specific medical contraindication (such as a specific allergy) is detailed in the raw documentation, use is strictly reserved for trained healthcare professionals. Misuse, outside the scope of oral surgery or for unintended functions, constitutes a de facto contraindication. It is essential to refer to the instructions for use before any intervention to identify any restrictions related to the patient's clinical condition or the nature of the alveolar bone. Compliance with sterilization protocols is also a sine qua non condition for its use in a surgical environment.

What are the precautions for use and maintenance?

As a non-resorbable and reusable instrument, the precautions for use for this Hu-Friedy elevator are based on rigorous handling and systematic maintenance. Before each use, the practitioner must carefully read the instructions provided by Hu-Friedy Mfg. Co., LLC. The instrument must be inspected to verify the integrity of the #23 tip and the #510 handle. Being a Class I device, it requires a complete cycle of cleaning, disinfection, and sterilization between each patient to prevent any risk of cross-contamination. The manufacturer emphasizes that this product is reserved for healthcare professionals, which implies a thorough knowledge of the force vectors to be applied to avoid any root fracture or damage to adjacent soft tissues.

Who is the manufacturer and what standards are respected?

The elevator #23 handle #510 is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is classified as a Class I medical device according to current regulations. Hu-Friedy is a globally recognized manufacturer for the quality of its surgical instruments. The product is subject to regulatory requirements regarding medical devices, ensuring its compliance for use in a professional clinical environment. Although specific CE marking is not mentioned in the source data, the Class I classification and the clear identification of the American manufacturer ensure traceability and compliance with the rigorous industrial manufacturing standards specific to the Hu-Friedy brand.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.