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

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The Luxateur hybride distal petit - 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)
  • Manufacturer

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Instrument

What is the Hu-Friedy small distal hybrid luxator?

The small distal hybrid luxator is a high-precision surgical instrument developed by Hu-Friedy Mfg. Co., LLC. This device from the CONSO category combines the properties of a traditional luxator and an elevator to optimize the initial stages of extraction. Its structure is adapted for intervention on distal surfaces, offering a technical response to the requirements of dental surgeons and implantologists. As a product designed by a recognized manufacturer such as Hu-Friedy, this tool meets the quality standards required for manual instrumentation in a clinical setting. Its specific design makes it a maneuverable small luxator for restricted spaces in the oral cavity.

What are the clinical indications for this luxator?

The use of this small distal luxator is indicated during tooth extraction procedures where precise separation of the periodontal ligament is necessary. It is particularly useful for practitioners performing avulsions prior to subsequent implant placement, as it helps in mobilizing the root. This extraction instrumentation is intended for use on teeth or roots located in a distal position, where standard instruments might lack finesse or approach angle. The manufacturer Hu-Friedy specifies that the use of this device is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of this instrument?

The small distal hybrid luxator is distinguished by its hybrid configuration which allows for both cutting ligament fibers and exerting a slight elevation force. Although specific materials are not detailed in the provided technical documentation, the product benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, located in Chicago. This small model luxator is classified as a Class I medical device, which corresponds to regulatory standards for non-invasive surgical instruments or those reusable after appropriate treatment. Its reduced size and distal orientation make it a specialized tool for posterior areas or narrow anatomies.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy, contraindications and indications are grouped under the intended use warnings. It is imperative that this small luxator not be used by individuals not trained in dental surgery procedures. General clinical contraindications apply, notably the inability to access the surgical site or systemic pathologies of the patient making the extraction dangerous. The practitioner must systematically refer to the instructions for use before any intervention to ensure the adequacy between the patient's clinical state and the use of this Class I instrument.

What are the precautions for use and maintenance?

Being a non-resorbable instrument of the extraction instrumentation type, this small luxator requires a strict protocol of cleaning, disinfection, and sterilization between each patient. Hu-Friedy emphasizes the importance of carefully reading the manual before use to guarantee patient safety and instrument longevity. Healthcare professionals must inspect the active tip of the small distal luxator before each procedure to detect any wear or deformation. Inappropriate handling, such as applying excessive leverage force for which the instrument is not designed, could damage the working part or compromise the integrity of the tooth socket.

Who is the manufacturer and what standards are respected?

The small distal hybrid luxator is manufactured by Hu-Friedy Mfg. Co., LLC, with its headquarters located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This manufacturer is globally recognized for the quality of its dental instrumentation. The product is listed as a Class I medical device. Compliance with Hu-Friedy manufacturing protocols ensures conformity with current regulatory requirements for manual surgical instruments. As a Class I device, it meets the safety and performance criteria defined for its category, thus guaranteeing reliable professional use within dental offices and oral surgery centers.


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Manufacturer Hu-Friedy
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