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Elevator number 92 handle number 510 upper mol. - Hu-Friedy - Delynov

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The Elévateur #92 manche #510 mol. supér. - 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.

127.35 € 127.35 EUR 127.35 € Tax Included

127.35 € Tax Included

(0.00 € / Units)
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Instrument

What is the #92 elevator #510 handle upper mol. - Hu-Friedy?

The #92 elevator with #510 handle is a manual surgical instrument developed by the manufacturer Hu-Friedy Mfg. Co., LLC. This device, belonging to the category of oral surgery instruments (INSTRU), is specifically configured for intervention on upper molars. Its structure includes an active working part designed to insert into the periodontal space and an ergonomic #510 type handle allowing for a firm grip during luxation maneuvers. This product is a Class I medical device, intended exclusively for professional use by practitioners trained in dental and implant surgery techniques.

What are the clinical indications?

This Hu-Friedy instrument is indicated for simple or complex exodontia procedures involving the molars of the upper arch. Its primary role is to ensure the initial luxation of the tooth by applying controlled leverage forces between the alveolar bone and the tooth root. It is used to break the ligament attachment and widen the socket, which facilitates subsequent extraction. The #92 elevator is particularly useful for the mobilization of upper molars presenting significant resistance or for the extraction of fractured roots located in the posterior zone, where access requires a specific angulation of the instrument.

What are the technical characteristics?

The #92 elevator is distinguished by its design adapted to the anatomy of upper molars. The #510 handle provides sufficient volume for effective force transmission without excessive fatigue for the surgeon. The working part is machined to guarantee precise insertion into the periodontal ligament. As a Hu-Friedy product, this instrument benefits from the expertise of the manufacturer Hu-Friedy Mfg. Co., LLC in metallurgy and surface finishing, ensuring adequate resistance to mechanical stresses encountered during luxation. This device is classified as Class I according to current regulations.

What are the contraindications for use?

According to 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 in the technical documentation other than those related to standard surgical extraction protocols. However, the practitioner must evaluate the condition of the alveolar bone and the proximity of adjacent anatomical structures, such as the maxillary sinus for upper molars, to avoid any complications. Use is prohibited for any person who does not have the clinical skills required to handle elevation instruments.

What are the maintenance precautions?

Although this product is non-resorbable as it is a metal instrument, strict reprocessing precautions apply. Before any use, it is imperative to carefully read the instructions for use provided by Hu-Friedy. Like any Class I surgical instrument, it must be cleaned, disinfected, and sterilized according to current hospital or office protocols (autoclave). The manufacturer Hu-Friedy emphasizes that the instrument is reserved for healthcare professionals and must be inspected before each intervention to check the integrity of the active part and the handle to ensure patient safety.

Who is the manufacturer and what standards are met?

The #92 elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device complies with Class I classification. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instruments. Compliance with manufacturing standards ensures that the instrument meets the safety and performance requirements expected for devices in its category. Professionals must ensure they follow the manufacturer's guidelines regarding intended use and warnings to maintain regulatory compliance during clinical use.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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