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Elevator Apex Number 301 with Handle Number 510 - Hu-Friedy - Delynov

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The Elévateur Apex #301 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 Apex #301 elevator #510 handle?

The Apex #301 elevator #510 handle is a precision manual instrument manufactured by Hu-Friedy, a recognized leader in the field of surgical instrumentation. This device consists of a specific active part, the Apex #301 tip, mounted on an ergonomic #510 type handle. It is specifically designed for oral surgery procedures requiring delicate manipulation of root structures. Its robust structure meets the requirements of practitioners during extraction phases. As a Class I medical device, it meets the manufacturing standards of Hu-Friedy Mfg. Co., LLC, guaranteeing a tool adapted to the constraints of the clinical environment.

What are the clinical indications for this instrument?

The apex 301 elevator is primarily indicated for the extraction of dental roots, fractured fragments, or root debris deeply lodged in the socket. In oral and implant surgery, it is used during the luxation phase, allowing for the rupture of ligament fibers before using forceps or to finalize the removal of residual roots. Its design is optimized to access narrow areas and ensure an effective grip on the root surface. The use of this instrument is exclusively reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, within the framework of conventional or surgical dental extraction protocols.

What are the technical characteristics of the Hu-Friedy elevator?

The instrument is distinguished by the combination of the Apex #301 tip and the #510 handle. The Hu-Friedy design ensures optimal force transmission during the leverage effect necessary for luxation. Although specific materials are not detailed in the provided technical documentation, manufacturing by Hu-Friedy Mfg. Co., LLC follows rigorous protocols specific to Class I devices. The #510 handle is designed to offer a stable grip, reducing fatigue during repeated procedures. The thinness of the Apex #301 tip allows for precise insertion into the periodontal space to mobilize the root without unnecessarily damaging the surrounding alveolar bone.

What are the contraindications for the use of this elevator?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for healthcare professionals. General clinical contraindications apply, notably use on bone or dental structures that do not allow for secure support, or in situations where excessive force could lead to a fracture of the bone plate. It is imperative to consult the instructions for use and respect the warnings provided by Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention. The practitioner must evaluate the appropriateness of the tool based on the patient's anatomy and the pathology being treated.

What are the maintenance precautions for this non-resorbable instrument?

As a reusable Class I surgical instrument, the Apex #301 elevator must undergo a strict protocol of cleaning, disinfection, and sterilization between each patient. Although composition specificities are not detailed, Hu-Friedy instruments generally require rigorous maintenance to preserve the integrity of the active tip and the handle. It is crucial to follow the manufacturer's maintenance recommendations to avoid any corrosion or premature degradation. Before each use, the professional must inspect the instrument to ensure the absence of cracks or marked wear that could compromise the safety of the surgical act or the effectiveness of the luxation.

Who is the manufacturer and what standards are respected?

The Apex #301 elevator #510 handle is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer emphasizes that the use of this instrument is reserved for duly trained healthcare professionals. Although specific CE marking is not mentioned in the source data, compliance with regulatory requirements for Class I devices is ensured by the manufacturer. Users are strongly advised to carefully read the instructions for use and warnings provided by Hu-Friedy to guarantee compliant and secure use in dental offices or hospital settings.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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