Lime for amalgam number 31/32 with handle number 41 - Hu-Friedy - Delynov
The Lime à amalgame #31/32 manche #41 - 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.
What is the Hu-Friedy #31/32 amalgam file with #41 handle?
The #31/32 amalgam file from the Hu-Friedy brand is a specific manual instrument intended for restorative dentistry procedures. Equipped with a #41 handle, this amalgam file is designed to provide a grip adapted to the requirements of practitioners during finishing work. Manufactured by Hu-Friedy Mfg. Co., LLC, it meets the quality standards of a recognized manufacturer in the field of surgical and dental instrumentation. This device is classified as a dental finishing instrument, essential for ensuring the longevity of amalgam restorations by working on the morphology and surface condition of the placed material.
What are the clinical indications for this instrument?
This amalgam finishing instrument is primarily indicated for the final carving and smoothing of restorations. Its use occurs after the condensation of the material to eliminate overfills and perfectly adapt the edges of the restoration to the cavity walls. In conservative surgery, the amalgam file allows access to interproximal and cervical areas where other rotary instruments might be less precise or more invasive to the surrounding soft tissues. It is reserved exclusively for healthcare professionals trained in these restorative techniques to guarantee safe and effective handling within the oral cavity.
What are the technical characteristics of the #31/32 amalgam file?
The #31/32 amalgam file is distinguished by its double configuration, allowing for alternating approach angles depending on the area being treated. The #41 handle is a technical reference at Hu-Friedy, offering a diameter and weight designed for comfort during clinical use. Although the exact composition is not specified, this dental finishing instrument is designed to withstand the sterilization cycles required in the practice. Its design allows for controlled abrasive action on the amalgam, facilitating the removal of excess without altering the integrity of the adjacent enamel. It is a precision tool for polishing and shaping metal restorative surfaces.
What are the contraindications for the use of this instrument?
According to data from the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed other than use being reserved for qualified healthcare professionals. However, as with any manual instrument, its use is contraindicated if the device shows signs of degradation or corrosion that could compromise patient safety or the effectiveness of the treatment. Application must be limited to the materials for which the instrument is designed, namely dental amalgam. The practitioner must always refer to the instructions for use and evaluate the specific clinical situation, particularly in cases of known hypersensitivity to the usual metallic components of the instrumentation.
What are the maintenance and handling precautions?
As a non-resorbable and reusable Class I instrument, the dental amalgam file requires a strict protocol of cleaning, disinfection, and sterilization between each patient. It is imperative to read the instructions carefully before use to comply with the sterilization parameters recommended by Hu-Friedy. The practitioner must ensure not to exert excessive pressure that could lead to a fracture of the working part or injury to the periodontal tissues. A visual inspection before each procedure is necessary to guarantee the absence of structural defects. Storage must be in a dry and clean environment to preserve the properties of the steel and the precision of the file.
Who is the manufacturer and what standards are met?
The #31/32 amalgam file is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a Hu-Friedy product, it benefits from the expertise of a historic manufacturer in the dental sector. Although CE marking is not explicitly specified in the source data, the product is strictly reserved for healthcare professionals and must be used in accordance with the warnings and instructions provided by the manufacturer. Compliance with these standards ensures that the instrument meets safety and performance requirements for dental finishing interventions in the practice.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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