Small Retentive Distal Cutting Pliers - Hu-Friedy - Delynov
The Pince coupante distale rétentive petite - 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 small retentive distal cinch back cutter?
The small retentive distal cinch back cutter, manufactured by Hu-Friedy Mfg. Co., LLC, is a specialized surgical instrument used primarily in orthodontics. This device is distinguished by its structure designed to cut metal archwires while retaining the cut segment. This dual function is crucial for patient safety, as it prevents the wire fragment from falling into the soft tissues or being ingested. As a product of the Hu-Friedy brand, this instrument benefits from the expertise of a recognized manufacturer in the field of high-precision dental instrumentation. Its reduced size is specifically adapted to cramped workspaces, facilitating manipulations in the posterior sectors of the oral cavity.
What are the clinical indications for this instrument?
This orthodontic distal cutter is indicated for the precise cutting of archwires during dental alignment treatments. It is particularly required during the initial placement of archwires or during follow-up appointments to adjust the length of the archwire protruding from molar tubes or bands. Its use is reserved for qualified healthcare professionals, such as orthodontists and dental surgeons, involved in oral surgery protocols or orthodontic follow-up. The integrated retentive mechanism allows for safe work in the distal zone, where visibility and access are often limited, ensuring that each wire section remains securely held by the instrument after cutting.
What are the technical characteristics of this cutter?
The Hu-Friedy retentive distal cutter features technical characteristics optimized for precision cutting. Although specific materials are not detailed in the source data, the instrument's design is based on engineering that allows for a clean cut of orthodontic wires. Its working head is dimensioned to reach the most remote areas of the dental arch without damaging surrounding tissues. The retention system is integrated into the jaws of the cutter, acting instantly upon the pressure exerted for cutting. This device is classified as a Class I instrument according to current regulations, meeting the quality and safety requirements for non-invasive medical devices used in daily dental practice.
What are the contraindications for the use of this device?
According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not exhaustively listed beyond standard warnings. However, the use of this instrument is strictly reserved for trained healthcare professionals. This cutter should not be used on materials or archwire diameters not intended by the manufacturer, which could damage the cutting or retention mechanism. As with any Class I instrument, a visual inspection before each use is recommended to ensure the absence of structural defects. Practitioners must systematically refer to the instructions for use provided by Hu-Friedy to identify any restrictions related to specific clinical protocols.
What are the precautions for use and maintenance?
As a non-resorbable and reusable instrument, the retentive cinch back cutter requires a rigorous maintenance protocol in accordance with Hu-Friedy guidelines. Before the first use and after each clinical act, the instrument must be cleaned, disinfected, and sterilized according to standard dental hygiene procedures. It is imperative to read the instructions carefully to respect the recommended sterilization cycles and preserve the integrity of the retention mechanism. Healthcare professionals must ensure the instrument is handled with care to avoid any impact on the cutting jaws, which would guarantee the longevity of the cutter and the precision of the distal cut during regular orthodontic interventions.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is a Class I medical device, which implies that it meets the safety and performance standards defined for this category of surgical instruments. The Hu-Friedy brand is synonymous with quality in the global dental industry, ensuring practitioners use reliable tools that comply with regulatory requirements. Although specific CE marking is not mentioned in the source data, the Class I classification and compliance with manufacturer warnings guarantee secure professional use. Users are invited to consult the technical documentation for any additional information on compliance.
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Specifications
| Manufacturer | Hu-Friedy |
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