Elevator number 9L with handle number 503 - Hu-Friedy - Delynov

What is the Hu-Friedy #9L elevator with #502 handle?

The #9L elevator with #502 handle, manufactured by Hu-Friedy Mfg. Co., LLC, is a manual instrument used in oral surgery to facilitate dental extraction. This INSTRU category device is designed to be inserted between the alveolar bone and the tooth root in order to break the periodontal ligament fibers. The Hu-Friedy brand is recognized for the quality of its surgical instruments, offering practitioners tools adapted to the requirements of implantology and oral surgery. This specific model combines a #9L type working part with an ergonomic handle referenced under number #502 for optimal handling during complex surgical procedures.

What are the clinical indications for this instrument?

The Hu-Friedy #9L elevator is primarily indicated for the luxation of teeth prior to avulsion. In oral and implant surgery, it is used to mobilize the tooth or root fragments, thereby facilitating an extraction that is less traumatic for the surrounding bone. Its use is reserved for qualified healthcare professionals, such as dental surgeons and stomatologists. It is used in simple or complex extraction protocols, particularly when preparing a site for future implant placement where preservation of the alveolar walls is crucial. The instrument allows for the application of precise leverage pressure to release the dental structure from its socket.

What are the technical characteristics of the #9L elevator?

This instrument is classified as a Class I medical device according to current regulations. It consists of a #9L active part and a #502 type handle, a configuration standardized by the manufacturer Hu-Friedy to meet the ergonomic needs of practitioners. Although the exact composition is not specified in the provided technical data, Hu-Friedy instruments are developed to withstand repeated sterilization cycles in a clinical environment. The design of the #502 handle ensures a stable grip, allowing for the transmission of axial and rotational force necessary for the effective luxation of dental roots without compromising the integrity of adjacent tissues.

What are the contraindications for the use of this elevator?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for healthcare professionals. General contraindications include use by untrained personnel or for applications not intended by the manufacturer. Although the source document does not list specific medical contraindications related to the material, the instructions for use should always be consulted before any intervention. As with any Class I instrument, the practitioner must evaluate the patient's clinical condition and ensure that the instrument is used in an appropriate surgical setting, respecting aseptic protocols and the mechanical resistance limits of the tool.

What are the maintenance and safety precautions?

The #9L elevator with #502 handle is a reusable instrument that requires a rigorous cleaning and sterilization protocol between each patient. Hu-Friedy recommends reading the instructions carefully before use to ensure patient safety and the longevity of the instrument. As a Class I device, it must be visually inspected before each use to detect any signs of wear or deformation of the #9L active part. Incorrect handling or the application of excessive force could damage the instrument or the patient's bone structures. Compliance with the warnings from the manufacturer, located in Chicago, USA, is imperative to maintain the compliance and effectiveness of the tool in the dental office.

Who is the manufacturer and what standards are met?

The #9L elevator with #502 handle is produced by Hu-Friedy Mfg. Co., LLC, a recognized manufacturer located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device belongs to Class I of the medical device classification. Manufacturing by Hu-Friedy guarantees compliance with industrial standards for surgical instrumentation. Although specific CE marking is not mentioned in the source documentation, the product complies with the regulatory requirements for devices of its class intended for use by healthcare professionals. Practitioners must comply with the indications and warnings provided by the manufacturer to ensure safe use in accordance with MDR standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.