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Instrument for Composite No. 6 Class 2-3-4-5 - Hu-Friedy - Delynov

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The Instrument à composite #6 Classe 2-3-4-5 - 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.

50.85 € 50.85 EUR 50.85 € Tax Included

50.85 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy composite instrument #6?

The Hu-Friedy brand composite instrument #6 is a manual device specifically designed for handling aesthetic restorative materials. Manufactured by Hu-Friedy Mfg. Co., LLC, this tool is intended for the application and modeling of composite resins. Its structure is adapted to the requirements of conservative dentistry, allowing for precise manipulation of materials before their polymerization. This device belongs to the hand instrument category (INSTRU) and meets the manufacturing standards of a globally recognized manufacturer in the dental sector.

What are the clinical indications for this instrument?

This instrument is indicated for performing direct composite restorations. It is particularly effective for treating class 2 cavities, but also extends to classes 3, 4, and 5. In dental surgery, its use allows for condensing the material, sculpting occlusal or proximal anatomy, and adjusting marginal contours. Its design is optimized for working with composites in different areas of the arch, ensuring precise adaptation of the restorative material to the walls of the prepared cavity.

What are the technical characteristics of this device?

The Hu-Friedy composite instrument #6 is characterized by a double-ended design, adapted to the different stages of modeling. As a class 2 composite instrument, it features specific working ends for the insertion and shaping of resins. The manufacturing quality of Hu-Friedy Mfg. Co., LLC guarantees a surface finish that minimizes the adhesion of composite materials, which facilitates the clinical procedure. This device is listed under the regulatory class Class I, confirming its status as a low-risk medical device for professional use in the office.

What are the contraindications for the use of this instrument?

Specific contraindications are not detailed in the technical documentation provided by the manufacturer Hu-Friedy, beyond standard warnings. As with any metallic instrument, its use may be contraindicated in patients with a known hypersensitivity to the constituent metals, although this is rare for non-invasive modeling instruments. It is imperative to refer to the instructions for use provided by the manufacturer to identify any usage restrictions related to specific clinical protocols or particular restorative materials.

What are the maintenance and handling precautions?

As a non-resorbable and reusable instrument, it requires a rigorous sterilization protocol between each patient. Health professionals must carefully read the instructions before use to comply with the cleaning and disinfection cycles recommended by Hu-Friedy. Careful handling is required to preserve the integrity of the working ends and avoid any deformation that could compromise the precision of the composite modeling. Maintenance must be performed in accordance with Class I directives to ensure clinical safety and the longevity of the device.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device according to current regulations. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets the safety and performance requirements for dental health professionals. Although specific CE marking is not mentioned in the source data, compliance with Class I indicates adherence to standard regulatory processes for manual dental surgery instruments.


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Specifications

Manufacturer Hu-Friedy
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