Buser periosteal elevator #6 handle - Hu-Friedy - Delynov

What is the Hu-Friedy Buser elevator handle #6?

The Buser elevator handle #6, designed by Hu-Friedy, is a high-quality surgical instrument dedicated to soft tissue management. This elevator instrument is distinguished by its specific ergonomic configuration, using the number 6 handle from the Hu-Friedy range to optimize control during critical phases of the intervention. Manufactured by Hu-Friedy Mfg. Co., LLC, this device is a tool of choice for demanding practitioners seeking a precise tactile response. It is primarily used to lift the periosteum from the bone in a controlled manner. As a Class I medical device, it meets strict regulatory requirements for use in a professional clinical environment.

What are the clinical indications for this elevator instrument?

This periosteal elevator instrument is indicated for a wide variety of oral surgery procedures, notably in implantology, periodontology, and general oral surgery. Its primary role is to allow the elevation of a full-thickness flap by cleanly separating the periosteum from the alveolar bone. It is particularly useful during implant site preparation, bone grafting, or periodontal plastic surgery. The use of the Hu-Friedy Buser elevator is strictly reserved for qualified healthcare professionals, thus ensuring handling in accordance with current surgical protocols to minimize tissue trauma.

What are the technical characteristics of this device?

The Hu-Friedy Buser elevator is characterized by the integration of a #6 handle, a specific dimension in the catalog of the manufacturer Hu-Friedy Mfg. Co., LLC, offering an optimal balance between weight and maneuverability. Although the exact composition is not specified in the source data, manufacturing by Hu-Friedy ensures a finish consistent with advanced surgical instrumentation standards. This device belongs to the INSTRU category and is classified as Class I according to medical device regulations. Its design is engineered to meet the constraints of repeated sterilization and intensive use in dental and oral surgery practices.

What are the contraindications for the use of this instrument?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond general warnings for use. However, the use of this elevator instrument is strictly reserved for healthcare professionals trained in oral surgery techniques. Use by unqualified personnel constitutes a major contraindication. It is imperative to read the instructions carefully before use to become familiar with all warnings from the manufacturer Hu-Friedy Mfg. Co., LLC. As with any surgical instrument, its use should be avoided if the integrity of the device is compromised or if sterility conditions are not guaranteed.

What are the precautions for use and maintenance?

As the Buser elevator is a non-resorbable and reusable instrument, it requires a strict protocol for cleaning, disinfection, and sterilization between each patient. Professionals must follow Hu-Friedy recommendations to preserve the quality of the periosteal elevator instrument over time. It is essential to check the condition of the active tips before each intervention to ensure the absence of deformations. Compliance with the sterilization cycles recommended by the manufacturer Hu-Friedy Mfg. Co., LLC is crucial to maintain the conformity of this Class I device and guarantee patient safety as well as the effectiveness of the surgical gesture during invasive procedures.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This Buser elevator is a Class I medical device, meaning it meets basic safety and performance standards for non-invasive or short-term surgical instruments. Hu-Friedy is a globally recognized manufacturer for the rigor of its manufacturing processes. Although CE marking is not specified in the source documentation, the product complies with the regulatory requirements applicable to devices of its class. Practitioners should refer to the attached instructions for use for any additional information on MDR compliance.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.