Elevator number 95 with handle number 502 - Hu-Friedy - Delynov

What is the Hu-Friedy elevator #95 handle #502?

The elevator #95 with handle #502 is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. It consists of a specific working part, the #95 model, mounted on an ergonomic handle of type #502. This device is designed to meet the requirements of dental surgeons during oral surgery procedures. Its structure is optimized to transmit the forces necessary for luxation while offering a stable grip. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation, guaranteeing a tool adapted to rigorous clinical protocols.

What are the clinical indications for this instrument?

This instrument is primarily indicated for simple or complex dental extraction. It is used to luxate the tooth by inserting it into the periodontal space in order to break the ligament attachments. Its use is common in oral surgery, periodontology, and implantology, particularly when preparing the socket for an atraumatic extraction. The practitioner uses elevator #95 to mobilize roots or root debris that cannot be grasped directly by a forceps. Its clinical application allows for the reduction of bone resistance surrounding the tooth, thus facilitating its final removal while preserving the integrity of the surrounding tissues.

What are the technical characteristics of the elevator #95 handle #502?

The elevator #95 is distinguished by its specific working geometry, associated with the #502 handle. The design of the tip is engineered to insert effectively into the alveolar space. The #502 handle provides a gripping surface allowing for precise tactile control during the application of lever forces. Manufactured by Hu-Friedy, this instrument is classified as a Class I medical device. Although the exact materials are not specified in the provided technical documentation, manufacturing follows the rigorous standards of Hu-Friedy Mfg. Co., LLC, ensuring mechanical resistance adapted to the constraints of dental luxation in a clinical environment.

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 qualified healthcare professionals. General contraindications include use on non-targeted anatomical structures or by personnel not trained in dental extraction techniques. Reference should systematically be made to the instructions for use and warnings provided by Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention. Any pathology or clinical condition of the patient making dental extraction risky must be evaluated beforehand by the surgeon; the instrument should only be used within the framework of a validated surgical protocol.

What are the maintenance and durability precautions?

As a non-resorbable instrument intended for repeated use after sterilization, the elevator #95 handle #502 requires rigorous maintenance. Although composition details are not provided, Class I instruments of this type must be cleaned, disinfected, and sterilized in accordance with hospital protocols and manufacturer instructions. It is imperative to check the integrity of the working tip before each use to ensure the absence of deformation or premature wear. Careful handling during dental extraction avoids excessive stress that could compromise the longevity of the instrument or injure the patient's soft tissues.

Who is the manufacturer and what standards are respected?

The elevator #95 handle #502 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 emphasizes that the use of this instrument is exclusively reserved for healthcare professionals. Compliance with manufacturing standards by Hu-Friedy guarantees that the instrument meets safety and performance requirements for dental surgery procedures. Practitioners must read the instructions carefully before use to ensure application in accordance with the manufacturer's guidelines and current standards of care.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.