Elevator Apex Number 9 with Handle Number 503 Straight - Hu-Friedy - Delynov

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

The #9 elevator with #502 handle, manufactured by Hu-Friedy, is a manual instrument used in oral surgery to facilitate tooth extraction. This device consists of an active working part, the n9 dental elevator, and a specific handle referenced as #502. This large handle is designed to provide an optimal contact surface with the surgeon's palm, allowing for efficient force transmission during rotation and leverage movements. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the field of high-precision dental instrumentation. This model is specifically intended for practitioners seeking a balance between control and power during the initial phases of exodontia.

What are the clinical indications for this instrument?

This instrument is primarily indicated for the luxation of teeth and root fragments. In oral and implant surgery, the n9 dental elevator is used after syndesmotomy to mobilize the tooth by breaking the periodontal ligament attachments. Its use is crucial for preparing the socket before the application of forceps, thereby reducing the risk of root fracture or damage to the surrounding alveolar bone. It is particularly useful in cases of simple or complex extractions where direct access and controlled leverage are required. This Hu-Friedy device is exclusively reserved for qualified healthcare professionals, ensuring application in accordance with current clinical protocols.

What are the technical characteristics of the #9 elevator with #502 handle?

The #9 elevator is distinguished by its technical configuration combining a robust working tip and an ergonomic #502 type handle. This large handle is a key feature for practitioners preferring a large handle dental elevator for better distribution of manual pressure. The design by Hu-Friedy Mfg. Co., LLC ensures structural integrity capable of withstanding repeated mechanical stress during luxation procedures. Although specific material details are not provided, the instrument meets the brand's manufacturing standards. It is a reusable instrument, requiring a strict sterilization protocol between each patient, in accordance with the instructions of the Chicago-based manufacturer.

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 include use on weakened bone structures where excessive leverage could cause an unwanted mandibular or maxillary fracture. It must not be used if the practitioner has not mastered the appropriate luxation technique or if the instrument shows signs of wear or deformation. It is imperative to read the instructions carefully before use to identify any specific warnings related to patient or practitioner safety. Compliance with indications and contraindications is essential to maintain the integrity of periodontal tissues.

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

As this is a metallic surgical instrument and not a resorbable device, precautions focus on the decontamination and sterilization cycle. Like any Class I Hu-Friedy instrument, the #9 elevator must be cleaned, disinfected, and sterilized after each intervention to prevent risks of cross-contamination. It is recommended to use appropriate cleaning solutions that do not alter the instrument's surface. Regular visual inspection of the #9 tip and the #502 handle is necessary to detect any corrosion or loss of sharpness. Rigorous maintenance extends the operational life of the instrument while ensuring the aseptic safety required in a surgical environment.

Who is the manufacturer and what standards are respected?

The #9 elevator with #502 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 Hu-Friedy is globally recognized for the quality of its surgical instruments. As a Class I product, it meets the safety and performance requirements defined by health authorities for non-invasive or invasive manual instruments for temporary use. Practitioners must systematically refer to the labeling and instructions for use provided by Hu-Friedy to ensure compliance with safety standards and specific usage protocols for this oral surgery equipment.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.