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

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

Le davier #23 manche #510 est un instrument manuel spécialisé destiné à la chirurgie orale et implantaire. Ce dispositif médical de Classe I se compose d'une partie active référencée #23 et d'un manche ergonomique de type #510. Il est spécifiquement développé pour répondre aux exigences des praticiens lors des phases de luxation en chirurgie orale. Cet instrument bénéficie de l'expertise d'un fabricant reconnu dans le domaine de l'instrumentation chirurgicale. Il est exclusivement réservé à l'usage des professionnels de santé qualifiés, garantissant une application conforme aux protocoles cliniques en vigueur en chirurgie orale et hospitalière.

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?

En tant qu'instrument non résorbable et réutilisable, les précautions d'emploi de cet élévateur Hu-Friedy reposent sur une manipulation rigoureuse et un entretien systématique. Avant chaque utilisation, le praticien doit lire attentivement la notice d'utilisation. L'instrument doit être inspecté pour vérifier l'intégrité de la pointe #23 et du manche #510. Étant un dispositif de Classe I, il nécessite un cycle complet de nettoyage, désinfection et stérilisation entre chaque patient pour prévenir tout risque de contamination croisée. Ce produit est réservé aux professionnels de la santé, ce qui implique une connaissance approfondie des vecteurs de force à appliquer pour éviter toute fracture radiculaire ou dommage aux tissus mous adjacents.

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.