Retractor Kicheloe Number 1 Handle Number 41 Gingival - Hu-Friedy - Delynov

What is the Hu-Friedy Kicheloe #1 retractor with #41 handle?

The Kicheloe #1 retractor with #41 handle is a precision instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed for the retraction of soft tissues in the oral cavity. As a surgical gum retractor, it keeps gingival tissues at a distance to provide maximum visibility of the operative site. Its structure includes a Kicheloe #1 working part mounted on an ergonomic #41 type handle, facilitating manipulation during clinical procedures. This instrument is classified as a Class I medical device, meeting regulatory requirements for non-invasive or short-term invasive manual surgical tools used in dental practice.

What are the clinical indications for this periodontal retractor?

The Kicheloe #1 periodontal retractor is indicated for a wide range of oral and periodontal surgery procedures. Its primary use lies in the atraumatic retraction of gingival flaps and surrounding soft tissues during debridement flaps, resective surgeries, or tissue regeneration. In implant surgery, it helps clear the alveolar ridge to facilitate drilling and implant placement. The use of this Hu-Friedy instrument helps secure the operative field by avoiding soft tissue interference with rotary or manual instruments, thus ensuring better surgical precision during periodontal interventions.

What are the technical characteristics of the #41 handle and the Kicheloe #1 tip?

The Kicheloe #1 retractor is distinguished by its specific design adapted to gingival anatomy. The #41 handle is selected to offer a stable grip, essential during prolonged retraction phases in surgery. The Kicheloe #1 working part features a curvature and width designed to fit the contours of the gum without exerting excessive pressure that could compromise tissue vascularization. Manufactured by Hu-Friedy, this instrument benefits from the manufacturer's expertise in metallurgy to ensure resistance to deformation. Although material details are not specified in the source data, the overall design aims to meet the requirements for repeated sterilization and durability in a clinical environment.

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 qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than those related to standard surgical practices. The practitioner must, however, evaluate the condition of the patient's soft tissues before use; severe inflammation or extreme tissue fragility may require particularly careful handling. As with any Class I instrument, it is imperative to read the instructions for use carefully and respect aseptic protocols to avoid any post-operative complications related to misuse or cross-contamination.

What are the maintenance precautions for this non-absorbable device?

The Kicheloe #1 retractor is a non-absorbable reusable surgical instrument. To ensure its longevity and patient safety, it must undergo a complete cycle of cleaning, disinfection, and sterilization between each use, in accordance with Hu-Friedy manufacturer instructions. It is recommended to use pH-neutral cleaning solutions to avoid any alteration of the instrument surface. Before each intervention, the professional must visually inspect the retractor to detect any signs of wear, corrosion, or deformation of the Kicheloe working part. Rigorous maintenance ensures the preservation of the instrument's mechanical properties and its performance as a surgical gum retractor during daily clinical acts.

Who is the manufacturer and what standards are met by this product?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This retractor is a Class I medical device. Manufacturing by Hu-Friedy, a recognized leader in dental instrumentation, guarantees that the instrument is designed according to rigorous quality standards for professional use. Although CE marking is not specified in the source data, the product complies with the regulatory requirements applicable to devices of its class for safe marketing. Users are invited to systematically refer to the manufacturer's instructions and warnings for use in accordance with the safety standards in force in the dental surgery sector.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.