Elevator Davis Number 1 with Handle Number 503 - Hu-Friedy - Delynov

What is the Davis #1 elevator with #502 handle?

The Davis #1 elevator with #502 handle is a manual surgical instrument developed by Hu-Friedy, a recognized manufacturer in the field of dental instrumentation. This device belongs to the category of guided bone regeneration (GBR) instruments. It consists of a specific active part, the Davis #1 model, mounted on an ergonomic handle referenced as #502. This assembly is designed to meet the requirements of oral surgery, offering a robust structure adapted to the mechanical constraints encountered during clinical interventions. As a Class I medical device, it meets the strict manufacturing standards imposed by Hu-Friedy Mfg. Co., LLC to ensure safe professional use.

What are the clinical indications?

The Davis #1 elevator with #502 handle is primarily indicated for oral surgery, periodontology, and implantology interventions. Its intended use concerns the manipulation, elevation, or detachment of structures during complex surgical procedures, particularly in guided bone regeneration (GBR) protocols. This instrument is used to facilitate access to the operative site or to prepare the site before the placement of implants or filling materials. In accordance with Hu-Friedy manufacturer guidelines, this instrument is exclusively reserved for qualified healthcare professionals, thus ensuring application according to the state of the art in dental and maxillofacial surgery.

What are the technical characteristics?

The Davis #1 elevator is distinguished by its technical configuration combining a Davis #1 active tip and a #502 type handle. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument benefits from the industrial expertise of the Chicago-based brand. Although specific materials are not detailed in the raw MDR documentation, the instrument's design is optimized for sterilization and reuse in clinical settings. It is classified as a Class I medical device, which attests to its compliance with basic regulatory requirements for non-invasive or transiently invasive surgical instruments. The technical reference Davis #1 defines the geometry of the tip for maximum efficiency during elevation.

What are the contraindications for use?

According to information provided by the manufacturer Hu-Friedy, specific contraindications are not exhaustively listed beyond the intended use. However, the use of this Davis #1 elevator is strictly reserved for healthcare professionals duly trained in oral surgery techniques. Inappropriate use by unqualified personnel constitutes a major contraindication. Furthermore, as with any surgical instrument, its use is contraindicated if the instrument shows signs of degradation or if sterility conditions are not guaranteed before the surgical act. It is imperative to carefully read the instructions for use and respect the warnings from the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA.

What are the maintenance and durability precautions?

The Davis #1 elevator with #502 handle is a non-resorbable instrument designed for repeated use after an appropriate cleaning and sterilization cycle. To maintain the integrity of this Hu-Friedy device, practitioners must rigorously follow the standard decontamination protocols in force in dental offices or hospital settings. Although the exact material is not specified, the durability of the instrument depends on compliance with the sterilization parameters recommended by the manufacturer. It is recommended to visually inspect the elevator before each intervention to ensure the absence of corrosion or deformation of the Davis #1 tip, thus guaranteeing the precision of the surgical gesture and patient safety.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, in accordance with the Medical Device Regulation (MDR). Hu-Friedy is a globally recognized manufacturer for the quality of its surgical instrumentation. Compliance with Class I indicates that the instrument meets the safety and performance requirements defined for this category of products. Healthcare professionals must refer to the instructions provided by Hu-Friedy to ensure use consistent with clinical standards. Traceability and compliance are ensured by the rigorous control processes established by the American manufacturer.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.