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Hybrid Large Distal Luxator - Hu-Friedy - Delynov Online Store

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The Luxateur hybride large distal - 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.

176.40 € 176.4 EUR 176.40 € Tax Included

176.40 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy large distal hybrid luxating instrument?

The large distal hybrid luxating instrument from the Hu-Friedy brand is a specialized manual instrument used in oral surgery. This hybrid device combines the properties of several extraction instruments to offer a robust solution during root mobilization. Manufactured by Hu-Friedy Mfg. Co., LLC, this tool is designed to meet the requirements of practitioners performing complex extractions. Its wide structure and distal orientation are specifically studied to intervene in posterior sectors where access is often restricted. As a Class I medical device, it complies with the rigorous manufacturing standards imposed by the Chicago-based manufacturer.

What are the clinical indications?

This distal luxating instrument is indicated for the luxation of teeth and roots during exodontia procedures. In oral and implant surgery, it is used to separate the periodontal ligament attachment from the alveolar wall. Its use is particularly relevant when preparing a site for immediate implant placement, where the preservation of bone plates is crucial. The instrument allows the luxation movement to be initiated precisely, thus facilitating the subsequent use of forceps. It is suitable for healthcare professionals trained in minimally invasive surgical extraction techniques.

What are the technical characteristics?

The large distal hybrid luxating instrument features an enlarged working part to maximize the contact surface with the dental root. Its distal design allows for optimal angulation to reach molars and difficult-to-access areas in the oral cavity. Hu-Friedy developed this instrument to ensure efficient force transmission while maintaining high tactile precision for the surgeon. This distal dental luxating instrument is a non-sterile instrument at the time of purchase, requiring an appropriate cleaning and sterilization protocol before each intervention, in accordance with the instructions provided by the manufacturer Hu-Friedy Mfg. Co., LLC.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond general use warnings. However, the use of this instrument is strictly reserved for qualified healthcare professionals. It must not be used outside of its intended use, namely dental luxation. Practitioners must assess bone density and the condition of the dental structure before application to avoid any unwanted root fracture. Careful reading of the instructions for use and manufacturer warnings is imperative before any clinical manipulation in a dental office or hospital setting.

What are the maintenance and durability precautions?

As a non-resorbable and reusable instrument, the large distal hybrid luxating instrument requires rigorous maintenance to guarantee its longevity and patient safety. After each use in surgery, the instrument must undergo a complete cycle of decontamination, cleaning, and sterilization. It is essential to check the integrity of the distal working part to ensure the absence of deformation or premature wear that could compromise its effectiveness. Compliance with steam sterilization protocols, according to the parameters recommended by Hu-Friedy, is indispensable to maintain the mechanical properties of the steel and prevent corrosion risks.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This luxating instrument is classified as a Class I medical device. The manufacturer emphasizes that the use of this instrument is exclusively reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, the product follows the regulatory directives applicable to Class I devices for dental surgery. Practitioners must systematically refer to the instructions for use provided by Hu-Friedy to ensure use in compliance with current safety standards.


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Manufacturer Hu-Friedy
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