Peeler Prichard Handle Number 522 Short - Hu-Friedy - Delynov

What is the Hu-Friedy Prichard periosteal elevator with #522 short handle?

The Prichard periosteal elevator with #522 short handle is a high-precision surgical instrument designed by the renowned manufacturer Hu-Friedy. This device, often referred to as a dental elevator or Prichard periosteal elevator, is specifically developed for oral surgery interventions. Its structure is distinguished by the integration of the #522 handle in a short version, offering a specific grip for practitioners working in cramped clinical spaces. As a Hu-Friedy brand instrument, it benefits from the expertise of Hu-Friedy Mfg. Co., LLC in periodontal instrumentation. This device belongs to the category of non-invasive or short-term invasive manual instruments used for the management of soft tissues and the periosteum.

What are the clinical indications for this Prichard periosteal elevator?

The use of this Prichard elevator is primarily indicated in periodontology and implant surgery. It is used for the elevation of a full-thickness flap, allowing the surgeon to expose the underlying bone with precision. Its role is crucial during the mucoperiosteal detachment phase, where it serves to detach the periosteum from the bone surface without lacerating the tissues. It is also used to maintain the flap in a retracted position, thus providing optimal visibility of the operative site during osteotomy or implant placement. This device is exclusively reserved for healthcare professionals trained in oral surgery techniques, in accordance with Hu-Friedy manufacturer guidelines.

What are the technical characteristics of this Hu-Friedy instrument?

The Hu-Friedy Prichard elevator is characterized by its robust design and meticulous finish. The specificity of this model lies in its short #522 handle, which modifies the center of gravity and the leverage of the instrument compared to standard handles. This technical feature is particularly sought after for interventions in posterior sectors or in patients with limited mouth opening. Although the exact composition is not specified in the source data, the manufacturing standards of Hu-Friedy Mfg. Co., LLC guarantee an instrument meeting the requirements of Class I. The geometry of the active tip is designed to follow the alveolar anatomical structures, thus facilitating efficient and controlled detachment.

What are the contraindications for the use of this dental elevator?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than those related to the inappropriate use of the instrument by untrained personnel. As with any Class I surgical instrument, its use must be preceded by a rigorous clinical evaluation of the patient's soft tissue condition. Use is contraindicated if the instrument shows signs of degradation or if sterility conditions are not guaranteed. The instructions for use should be systematically consulted before any intervention.

What are the maintenance and handling precautions?

Although this elevator is not a resorbable device, its durability and safety of use strictly depend on compliance with cleaning and sterilization protocols. As a Class I medical device manufactured by Hu-Friedy, it must be processed according to the specific instructions of the manufacturer located in Chicago, USA. Practitioners must take care not to exert excessive torsional forces that could compromise the integrity of the active tip or the short #522 handle. Before each use, a visual inspection is necessary to ensure the absence of corrosion or micro-cracks. Compliance with the sterilization cycles recommended by Hu-Friedy is essential to maintain the mechanical properties of the instrument and guarantee patient safety.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This Prichard elevator is classified as a Class I medical device. The CE marking is not specified in the technical data available for this specific reference, but the product respects the rigorous quality standards imposed by the Hu-Friedy brand, a recognized player in the surgical instrumentation sector. Professionals must carefully read the notice and warnings provided by the manufacturer to ensure use in accordance with current regulatory requirements. Traceability and compliance with American and international manufacturing standards are at the heart of Hu-Friedy's production processes.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.