Rasp for Bone Miller number 52 handle number 522 - Hu-Friedy - Delynov

What is the Hu-Friedy Miller #52 bone file with #522 handle?

The Miller #52 bone file, associated with the #522 handle, is a high-precision manual instrument manufactured by Hu-Friedy. This device is specifically designed for working on hard tissues during oral surgery procedures. Its structure allows for controlled handling for bone remodeling. As a product developed by Hu-Friedy Mfg. Co., LLC, this instrument meets the quality requirements of demanding practitioners. It is classified as a Class I medical device, which guarantees its compliance with regulatory standards for non-invasive surgical instruments or those reusable after sterilization according to current protocols.

What are the clinical indications for this instrument?

La lime Hu-Friedy Miller #52 est principalement indiquée pour la régularisation des crêtes alvéolaires et le lissage des spicules osseux. En chirurgie orale et implantologie, elle est utilisée après des extractions multiples ou lors d'alvéoloplasties pour éliminer les aspérités susceptibles de compromettre la cicatrisation des tissus mous ou l'ajustement d'une prothèse. Son usage est strictement réservé aux professionnels de santé qualifiés, tels que les chirurgiens oraux et les stomatologues, opérant dans des contextes de chirurgie parodontale ou pré-implantaire nécessitant une préparation méticuleuse du site osseux.

What are the technical characteristics of the Miller #52 file?

The Miller #52 bone file is distinguished by its serrated working part, designed for effective but controlled abrasion of bone tissue. The #522 handle offers a grip adapted to repetitive filing motions, allowing for optimal force transmission without sacrificing the tactile sensitivity necessary to assess the surface condition of the bone. Manufactured by Hu-Friedy, this instrument benefits from the technical expertise of the Chicago-based manufacturer. The design of the Miller series is recognized for its ability to access difficult areas, thus offering technical versatility during complex bone remodeling procedures.

What are the contraindications for the use of this device?

L'utilisation de cet instrument est strictement réservée aux professionnels de santé qualifiés. Bien qu'aucune contre-indication médicale spécifique liée à un matériau n'ait été répertoriée, les protocoles cliniques standard doivent être respectés. L'instrument ne doit pas être utilisé en dehors de son usage prévu, à savoir le limage osseux. Une utilisation inappropriée sur les tissus mous ou des matériaux non biologiques pourrait endommager la partie travaillante ou provoquer un traumatisme iatrogène. Il est impératif de consulter la notice d'utilisation avant toute utilisation pour s'assurer de son adéquation au cas clinique.

What are the maintenance and durability precautions?

As a non-resorbable Class I instrument, the Hu-Friedy Miller #52 bone file requires a rigorous sterilization protocol between each patient. Although composition specifications are not detailed here, instruments in this category require thorough cleaning of the serrations to remove bone debris before autoclaving. Compliance with the cleaning instructions from the manufacturer Hu-Friedy Mfg. Co., LLC is essential to maintain the cutting efficiency of the file teeth. Regular inspection of the condition of the serrations and the integrity of the #522 handle is recommended to ensure safety during surgical procedures.

Who is the manufacturer and what standards are respected?

The Miller #52 bone file is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I. As a recognized manufacturer in the dental sector, Hu-Friedy ensures that this instrument is intended exclusively for professional use. Although specific CE marking is not mentioned in the source data, the product follows the regulatory directives applicable to devices of its class. Practitioners should refer to the official indications and warnings provided by the manufacturer to ensure use in accordance with current safety standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.