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Ortho Ligature Director Filion #6 Handle <=0.015 inch - Hu-Friedy - Delynov

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The Ortho Ligatures Director Filion manche #6 <=0.015 inch - 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.

91.20 € 91.2 EUR 91.20 € Tax Included

91.20 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Ortho Ligatures Director Filion?

The Ortho Ligatures Director Filion is a specialized instrument designed by Hu-Friedy Mfg. Co., LLC for orthodontic practitioners. This device, featuring a #6 type handle, is specifically developed for manipulating ligatures on archwires with a diameter less than or equal to 0.015 inch. Manufactured by Hu-Friedy, a recognized manufacturer in the field of surgical and dental instrumentation, this tool allows for rigorous management of orthodontic components during the placement or adjustment of multi-bracket appliances. Its structure is designed to provide a reliable interface between the practitioner's hand and the fine elements of the appliance.

What are the clinical indications for this ortho ligature instrument?

This ortho ligature instrument is indicated for ligating procedures in clinical orthodontics. Its primary use lies in guiding ligatures around brackets and adjusting archwires into the fixation slots. It is particularly recommended when using fine section wires (≤0.015 inch), where precision of movement is crucial to avoid any undesirable deformation of the archwire. As an orthodontic ligature director, it assists the healthcare professional in the secure placement of metallic or elastic ligatures, thereby ensuring optimal transmission of the orthodontic forces planned in the treatment plan.

What are the technical characteristics of the Filion orthodontic ligature director?

The Filion orthodontic ligature director features precise technical specifications to meet the requirements of orthodontists. It is equipped with a number 6 handle, offering ergonomics adapted to meticulous interventions. Its working part is calibrated to interact with wires of a maximum diameter of 0.015 inch. This device is part of the Hu-Friedy instrumentation range, guaranteeing compliance with the brand's manufacturing standards. As a Class I instrument, it meets the basic regulatory requirements for non-invasive medical devices used in dental and orthodontic offices.

What are the contraindications for the use of this instrument?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than use by untrained personnel or use diverted from its initial function as a ligature director. Practitioners should refer to the manufacturer's warnings located at 3232 N. Rockwell St. Chicago, Il 60618 USA. As with any metallic instrument, it is advisable to check for the absence of known allergies to standard components of orthodontic instrumentation before any intraoral intervention.

What are the maintenance precautions for this non-absorbable instrument?

Although the term resorption does not apply to metallic instrumentation, the durability of this Filion ligature instrument depends on compliance with sterilization and cleaning protocols. As a reusable Class I device, it must be systematically decontaminated, cleaned, and sterilized before each use in accordance with Hu-Friedy instructions and current hygiene standards. It is imperative to read the instructions carefully before use to ensure that sterilization cycles do not damage the mechanical properties of the instrument, particularly at the active tip intended for 0.015 inch wires.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This product is classified as a Class I medical device, which implies that it meets the safety and performance criteria defined for this regulatory category. The mention of Class I confirms its status as a regulated medical device. Hu-Friedy is a globally recognized manufacturer for the quality of its instruments. Healthcare professionals must consult the instructions for use and respect the manufacturer's warnings to guarantee compliant and safe use within their clinical practice.


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Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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