Miller #64 Bone Rasp with #522 Handle - Hu-Friedy - Delynov

What is the Miller #64 bone file with #522 handle?

The Miller #64 bone file with #522 handle is a manual surgical instrument manufactured by Hu-Friedy. This device is specifically designed for practitioners performing oral surgery and implantology procedures. Its structure includes a Miller #64 working part mounted on a reference #522 handle, offering a grip adapted to the requirements of clinical practice. As an instrument in the Hu-Friedy range, it meets the quality standards of a recognized manufacturer in the dental sector. This device is classified as a Class I instrument according to current regulations, guaranteeing its compliance for professional use in dental offices or hospital settings.

What are the clinical indications for this dental surgical file?

This dental surgical file is primarily indicated for the smoothing and remodeling of bone structures. In oral surgery, it is used during alveoloplasty procedures to regularize alveolar ridges after multiple extractions. It effectively removes bone irregularities, spicules, or exostoses that could compromise soft tissue healing or the fit of a removable prosthesis. In implantology, it is used to prepare the recipient site by smoothing bone contours, thus ensuring a stable and uniform base. Its use is strictly reserved for qualified healthcare professionals mastering bone surgery techniques.

What are the technical characteristics of this instrument?

The Miller #64 file is characterized by a specific configuration of its active part, optimized for controlled abrasion of hard tissues. The associated #522 handle is designed by Hu-Friedy to ensure adequate balance during manipulation, allowing precise transmission of the force applied by the surgeon. Although specific material details are not provided, Hu-Friedy instruments are recognized for their resistance to repeated sterilization cycles. This device is a non-sterile instrument upon delivery, requiring a rigorous cleaning and sterilization protocol before each use, in accordance with the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC located in Chicago.

What are the contraindications for the use of this device?

The contraindications related to the use of the Miller #64 bone file are linked to clinical oral surgery protocols. According to information from the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for healthcare professionals. It must not be used in situations where rotary instrumentation is deemed more appropriate for patient safety or when surgical access does not allow for sufficient visual and manual control. It is imperative to consult the instructions for use to identify any specific contraindication related to the patient's systemic state or potential hypersensitivities to components of conventional surgical instrumentation.

What are the maintenance and handling precautions?

As a non-resorbable Class I instrument, the longevity of the Miller #64 file depends on its maintenance. The practitioner must ensure to inspect the condition of the working part before each intervention to detect any signs of wear or corrosion. Cleaning must be performed immediately after use to prevent the encrustation of organic debris. It is recommended to use neutral pH cleaning solutions and to scrupulously follow the steam sterilization cycles recommended by Hu-Friedy. Careful handling is necessary to preserve the sharpness of the file's serrations, thus guaranteeing its effectiveness during bone smoothing in implant or periodontal surgery.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, Il 60618, USA. This product is a Class I medical device. Manufacturing by Hu-Friedy ensures compliance with the rigorous quality control processes specific to medical devices intended for dental surgery. Users must imperatively read the attached instructions for use carefully before any implementation. The regulatory compliance of this instrument guarantees that it meets safety and performance requirements for bone remodeling interventions, subject to use by duly trained medical personnel.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.