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Instrument composite n°1 with handle n°41 for anterior teeth - Hu-Friedy - Delynov

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The Instrument à composite #1 manche #41 antérieur - 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 #1 composite instrument with #41 anterior handle?

The #1 composite instrument with #41 handle is a manual device developed by the manufacturer Hu-Friedy for restorative care. This specific model is configured for work on anterior teeth, where aesthetic precision is paramount. Its structure is optimized for the manipulation of composite resins, allowing for efficient transfer and modeling of the material without altering its physical properties before polymerization. As a Hu-Friedy brand product, this instrument meets the manufacturing standards of a recognized player in the dental sector, guaranteeing seamless integration into the direct restoration protocol.

What are the clinical indications for this instrument?

This instrument is indicated for restorative dentistry procedures involving the use of restorative composites, particularly in the anterior sector (incisors and canines). It is used for placing, sculpting, and smoothing filling materials in Class III, IV, and V cavities. Its design allows for defining anatomical contours, managing embrasures, and smoothing surfaces before hardening. Practitioners use it during composite layering to ensure perfect adaptation to the preparation margins, thus minimizing the risk of air bubbles or interface defects.

What are the technical characteristics of this instrument?

The Hu-Friedy #1 composite instrument is distinguished by its #41 handle, offering a specific grip adapted to the fine movements required in the anterior zone. Although precise alloy details are not specified, manufacturing by Hu-Friedy Mfg. Co., LLC ensures quality compliant with Class I device requirements. The working ends are designed to limit composite adhesion, thus facilitating modeling without deforming the resin structure. The lightness and balance of the #41 handle contribute to reducing fatigue during complex restoration sessions, allowing for optimal tactile control during the application of material layers.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications include any clinical situation where access to anterior cavities is restricted or when the use of manual instruments is not suitable for the chosen restoration technique. Although the raw MDR text does not list specific medical contraindications related to materials, it is imperative to read the instructions carefully before use to identify any particular warnings. Compliance with sterilization protocols is mandatory to avoid any cross-contamination.

What are the maintenance and handling precautions?

As a non-resorbable and reusable Class I instrument, it requires a complete cycle of decontamination, cleaning, and sterilization between each patient. Practitioners must follow the instructions from Hu-Friedy Mfg. Co., LLC regarding compatible cleaning agents to preserve the integrity of the working ends. Careful handling is required to avoid damaging the active parts, which could compromise the quality of the composite modeling. It is recommended to inspect the instrument before each use to ensure the absence of residues or physical degradation that could impact clinical precision during care.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. Hu-Friedy is a manufacturer recognized for its compliance with rigorous production standards in the field of instrumentation. The product is intended exclusively for healthcare professionals, and its use must be preceded by a careful reading of the provided instructions for use. Compliance with Class I regulatory requirements ensures that the device meets safety and performance standards for its intended use in dental surgery.


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Manufacturer Hu-Friedy
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