Prichard #3 periosteal elevator #522 handle - Hu-Friedy - Delynov

What is the Prichard #3 periosteal elevator handle #522?

The Prichard #3 periosteal elevator, combined with the #522 handle, is a manual surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed for oral surgery procedures where separation of the periosteum from the bone is required. As an instrument in the INSTRU category, it features a configuration suitable for the retraction and lifting of soft tissue flaps. Its design meets the requirements of clinical practice in implantology and periodontology, providing the practitioner with a reliable tool for exposing bony surgical sites. This product is exclusively reserved for use by qualified healthcare professionals.

What are the clinical indications?

Clinical indications for the Hu-Friedy Prichard #3 periosteal elevator include any intervention requiring full-thickness flap elevation. It is commonly employed in periodontal surgery for access to roots or during resection surgeries. In implantology, this instrument facilitates the exposure of the alveolar ridge prior to drilling or implant placement. It is also indicated for guided bone regeneration (GBR) procedures where precise soft tissue management is crucial to ensure primary closure of the site. The intended use, as defined by Hu-Friedy, falls within a strict professional surgical framework.

What are the technical characteristics?

The Prichard #3 periosteal elevator is characterized by its #522 reference handle, offering a grip adapted to the requirements of micro-surgery and standard oral surgery. Although specific materials are not detailed in the provided MDR documentation, this instrument is a Class I device, which attests to its compliance with basic regulatory requirements for non-invasive or transiently invasive surgical instruments. The double or single-ended design, typical of Hu-Friedy Prichard instruments, is optimized to minimize tissue trauma during periosteal separation, ensuring smooth manipulation on bone surfaces.

What are the contraindications for use?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not exhaustively listed in the raw MDR text, beyond the obligation for use by healthcare professionals. Generally, in oral surgery, the use of this instrument is contraindicated in patients with severe systemic pathologies that do not allow for surgical intervention, or in cases of known allergies to the metallic components of surgical instruments. It is the practitioner's responsibility to evaluate the benefit/risk ratio based on the patient's clinical status and to carefully read the instructions before any use.

What are the precautions for use and maintenance?

Like any Class I surgical instrument from the Hu-Friedy brand, the Prichard #3 periosteal elevator must be used with care to avoid damaging adjacent anatomical structures. Although non-absorbable since it is a reusable metallic instrument, it requires a rigorous sterilization protocol before each intervention. Healthcare professionals must refer to the cleaning and sterilization instructions provided by Hu-Friedy to maintain the integrity of the instrument. A visual inspection before use is recommended to ensure the absence of corrosion or deformation of the working parts, thus guaranteeing patient safety and the effectiveness of the surgical procedure.

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 Prichard #3 periosteal elevator is classified as a Class I medical device according to current regulations. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures quality consistent with international dental surgery requirements. It is imperative to read the instructions carefully before use to ensure compliance with safety protocols.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.