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

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The Râpe à os Miller #52 manche #522 - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

138.45 € 138.45 EUR 138.45 € Tax Included

138.45 € Tax Included

(0.00 € / Units)
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Instrument

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?

The Hu-Friedy Miller #52 file is primarily indicated for the regularization of alveolar ridges and the smoothing of bone spicules. In implant and oral surgery, it is used following multiple tooth extractions or during alveoloplasties to eliminate roughness that could compromise soft tissue healing or the fit of a prosthesis. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, operating in periodontal or pre-implant surgery contexts requiring meticulous preparation of the bone site.

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?

According to information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for trained healthcare professionals. Although no specific medical contraindications related to a material have been listed in the source documentation, standard clinical protocols must be followed. The instrument must not be used outside of its intended use, namely bone filing. Inappropriate use on soft tissues or non-biological materials could damage the working part or cause iatrogenic trauma. It is imperative to consult the instructions before any use to ensure suitability for the clinical case.

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.


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Manufacturer Hu-Friedy
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