Prichard periosteal elevator #3M handle #522 curved

What is the Prichard #3M periosteal elevator?

The Prichard #3M periosteal elevator is a high-precision surgical instrument manufactured by Hu-Friedy, a recognized manufacturer in the field of medical instrumentation. This specific model is distinguished by its #522 handle featuring a curved shape, optimizing access to complex anatomical areas of the oral cavity. It is primarily used to separate the periosteum from the bone, a crucial step in creating full-thickness flaps. Its structure is designed to offer a stable grip, allowing the practitioner to exert controlled force during subperiosteal dissection. As a Hu-Friedy brand instrument, it benefits from a rigorous design meeting the requirements of oral surgery operating rooms.

What are the clinical indications for this instrument?

The Prichard #3M periosteal elevator is indicated for a variety of procedures in oral, periodontal, and implant surgery. Its primary use lies in the elevation of mucoperiosteal flaps, allowing exposure of the underlying alveolar bone. It is particularly sought after during implant placement, bone grafting, or soft tissue corrective surgeries. Its curved design facilitates navigation in posterior areas or sectors with reduced visibility. This Hu-Friedy instrument is exclusively reserved for qualified healthcare professionals, ensuring handling in accordance with current surgical protocols. It allows for clean tissue separation while preserving the integrity of the periosteum, a determining factor for post-operative vascularization and healing.

What are the technical characteristics of this periosteal elevator?

Technically, this device is characterized by its Prichard #3M reference associated with the curved #522 handle. This specific curvature is designed to improve ergonomics and the angle of approach during tissue elevation. Unlike straight handles, the #522 handle offers better visibility of the surgical field by clearing the surgeon's line of sight. The working end is sized to fit effectively under the incision edges without causing undesirable tissue tearing. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument complies with Class I manufacturing standards. The surface finish is optimized to resist repeated sterilization processes in a clinical environment, ensuring longevity in line with the expectations of specialized practices.

What are the contraindications for the use of this instrument?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for trained healthcare professionals. General clinical contraindications apply, notably use on tissues presenting uncontrolled acute infectious pathologies or extreme tissue fragility that would not allow for safe dissection. It is imperative to read the instructions carefully before use to become familiar with all warnings. Inappropriate use by unqualified personnel constitutes a major contraindication, as does using the instrument for functions other than those intended by its design (for example, as a lever on rigid non-bone structures).

What are the maintenance and handling precautions?

As the Prichard #3M periosteal elevator is a non-resorbable and reusable instrument, it requires a rigorous decontamination and sterilization protocol after each intervention. Although composition details are not specified, handling must be done with care to avoid any alteration of the curved working end. It is recommended to check the integrity of the instrument before each use, ensuring the absence of corrosion or deformation. Storage must be carried out in a dry and clean environment. Compliance with the sterilization cycles recommended by the manufacturer Hu-Friedy is essential to maintain the mechanical properties of the #522 handle and guarantee patient safety. Any rough handling could compromise the precision of the technical curvature.

Who is the manufacturer and what standards are respected?

The Prichard #3M periosteal elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device belongs to Class I according to current regulations. The manufacturer emphasizes the importance of consulting the attached instructions for use to ensure use in accordance with safety standards. As a Class I product, it meets the quality and traceability requirements imposed for manual surgical instruments. Hu-Friedy is a globally recognized entity for the reliability of its instruments, providing practitioners with compliance with current regulatory expectations in the dental and oral surgery sector.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.