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Elevator Curtis Number 52 with Handle Number 510 - Hu-Friedy - Delynov

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The Elévateur Curtis #52 manche #510 - 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 curtis #52 elevator with #510 handle?

The curtis #52 elevator with #510 handle is a specialized oral surgery instrument manufactured by Hu-Friedy Mfg. Co., LLC. It consists of an active working part and an ergonomic handle referenced under number #510. This instrument is intended for extraction procedures in dental practices and hospital environments. As a Class I medical device, it meets the regulatory requirements for reusable surgical instruments. Its structure is designed to withstand mechanical stress during dental luxation, providing the practitioner with a grip adapted to oral surgery procedures.

What are the clinical indications for this instrument?

The dental curtis elevator is primarily indicated for the luxation of teeth and roots during simple or complex extractions. Its clinical role is to separate the epithelial attachment and break the periodontal ligaments using a lever or rotation movement. It is used by dental surgeons and stomatologists to prepare the socket before final extraction. This instrument is particularly useful in cases of fractured roots or impacted teeth where access is limited, allowing for effective mobilization of the dental unit while preserving the integrity of the surrounding alveolar bone.

What are the technical characteristics of this elevator?

The Curtis #52 elevator is distinguished by its specific configuration combining the Curtis active tip with the #510 handle from the Hu-Friedy brand. This handle is designed to offer optimal control when applying the leverage forces required in oral surgery. Although specific materials are not detailed in the provided technical documentation, the manufacturing standards of Hu-Friedy Mfg. Co., LLC guarantee an instrument compliant with Class I requirements. The geometry of the #52 tip is designed to insert precisely into the periodontal space, thus facilitating luxation maneuvers without compromising the bone structure.

What are the contraindications for the use of this instrument?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed outside of standard oral surgery protocols. However, the use of the curtis elevator is contraindicated if the practitioner has not mastered luxation techniques, as excessive force could lead to a fracture of the bone plate or the root. It is imperative to consult the instructions for use and respect the warnings from the manufacturer located in Chicago, USA, to ensure patient safety during the intervention.

What are the maintenance and sterilization precautions?

As a Class I oral surgery instrument, this Curtis elevator must be cleaned, disinfected, and sterilized before each use in accordance with the protocols in force in dental practices. Although the resorption process does not apply to this non-implantable instrument, its durability depends on compliance with the cleaning instructions from the manufacturer Hu-Friedy. It is recommended to use appropriate cleaning solutions to avoid any corrosion and to check the integrity of the active tip before each surgical act. Regular visual inspection ensures the absence of micro-cracks or deformations due to repeated sterilization cycles.

Who is the manufacturer and what standards are respected?

The Curtis #52 elevator is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer is recognized for its expertise in the design of high-precision dental instruments. Healthcare professionals must read the instructions carefully before any use to ensure compliance with safety and efficacy standards. Although CE marking is not specified in the source data, the instrument follows the strict directives imposed on Class I medical devices intended for oral surgery.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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