Elevator number 94 with handle number 502 - Hu-Friedy - Delynov

What is the #94 elevator #502 handle - Hu-Friedy?

The #94 elevator with #502 handle is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This Class I device is specifically designed for oral surgery procedures requiring effective luxation. Its structure consists of a working part referenced as #94 and an ergonomic handle of type #502. As a Hu-Friedy brand instrument, it meets the quality requirements of practitioners for extraction procedures. This device is strictly reserved for healthcare professionals trained in dental and implant surgical techniques. It constitutes a standard tool in the arsenal of the general practitioner or oral surgeon for the treatment of non-restorable dental structures.

What are the clinical indications for this instrument?

The clinical indications for this Hu-Friedy elevator primarily concern simple or complex tooth extraction. It is indicated for the luxation of teeth, fractured roots, or apices remaining in the socket. In implant surgery, it can be used to prepare the extraction site while optimally preserving the alveolar bone walls. The intended use, as defined by the manufacturer Hu-Friedy Mfg. Co., LLC, is limited to surgical acts performed by qualified professionals. The instrument allows for the initiation of tooth mobility by breaking the ligament fibers, thus facilitating the subsequent use of forceps. It is essential to follow current clinical protocols to ensure use in accordance with the indications of the manufacturer located in Chicago.

What are the technical characteristics of the #94 elevator?

The #94 elevator is distinguished by the configuration of its active part, optimized to insert into the periodontal space. The accompanying #502 handle is designed to offer a stable grip, allowing for the transmission of necessary rotational and leverage forces without compromising control of the movement. This medical device belongs to Class I according to current regulations. Manufactured by Hu-Friedy, the instrument benefits from the manufacturer's metallurgical expertise to ensure adequate resistance during mechanical stress. Although exact material specifications are not detailed here, the design is oriented toward durability and compatibility with standard dental office sterilization cycles.

What are the contraindications for the use of this elevator?

According to the information provided by Hu-Friedy Mfg. Co., LLC, specific contraindications are not listed exhaustively beyond the use being reserved exclusively for healthcare professionals. However, from a general clinical perspective, the use of this instrument is contraindicated in patients presenting with severe local bone pathologies or uncontrolled general contraindications to oral surgery. It must not be used by unqualified persons. The practitioner must evaluate the benefit/risk ratio before any intervention. It is imperative to read the instructions carefully and respect the manufacturer's warnings regarding maintenance and use to avoid any risk of instrument breakage or injury to adjacent tissues.

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

As a reusable and non-resorbable metallic surgical instrument, the #94 elevator #502 handle requires a rigorous decontamination and sterilization protocol after each use. Although the source text does not detail the exact process, it is standard practice in surgery that these Hu-Friedy devices are cleaned, disinfected, and sterilized in an autoclave according to dental practice standards. Compliance with the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC is paramount to maintain the integrity of the active part and the handle. A visual inspection before each intervention is recommended to detect any signs of wear, corrosion, or deformation that could compromise patient safety or the effectiveness of the surgical act.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I, which corresponds to devices presenting a low degree of risk according to medical device regulations. As a Hu-Friedy product, it is manufactured under recognized quality control standards. CE marking is not specified in the current source data, but the product is explicitly intended for the healthcare professional market. Users must imperatively read the instructions and comply with the manufacturer's warnings to ensure safe use in accordance with international regulatory requirements.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.