Periodontal Scissors with Backward Action, Short Handle Number 6 - Hu-Friedy - Delynov

What is the Hu-Friedy #9 knife #40 gold-plated handle?

The #9 knife with #40 gold-plated handle is a specialized manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device, belonging to the surgical instrument category, is designed to provide a response adapted to the requirements of practitioners during tissue cutting phases. It is distinguished by its specific configuration including a #40 handle with a gold-plated finish, facilitating identification and handling during operative acts. As a Hu-Friedy product, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation, guaranteeing a tool that complies with professional standards for interventions in private practice or hospital settings.

What are the clinical indications for this dental surgery knife?

This dental surgery knife is primarily indicated for oral and periodontal surgery procedures. Its use is intended for the excision, incision, and reshaping of soft tissues, particularly during gingivectomies or gingivoplasties. It allows the surgeon to perform precise movements on the keratinized or alveolar mucosa. In accordance with Hu-Friedy guidelines, this instrument is exclusively reserved for qualified healthcare professionals. Its application extends to implantology interventions where flap management requires fine instrumentation to ensure optimal healing of peri-implant soft tissues.

What are the technical characteristics of this instrument?

The #9 knife #40 gold-plated handle is characterized by its robust design and its Class I regulatory classification. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the rigorous manufacturing requirements of the Chicago, USA site. The #40 handle with gold finish (gold-plating) allows for rapid visual distinction within the surgical tray. Although specific materials are not detailed in the provided technical documentation, the instrument is designed to withstand standard sterilization cycles in clinical environments. Its geometry is optimized to ensure efficient force transmission during incision, while maintaining strict directional control during the surgical act.

What are the contraindications for the use of this device?

According to data from the manufacturer Hu-Friedy, specific contraindications related to the patient's health status are not exhaustively listed in the raw MDR text. However, the use of this instrument is strictly reserved for healthcare professionals who have received adequate training. This device should not be used outside of its intended use, namely soft tissue surgery. Practitioners must assess the risks of potential allergies to metallic components before any intervention. As with any Class I instrument, a visual inspection before use is imperative to detect any wear or damage that could compromise patient safety or the effectiveness of the surgical procedure.

What are the precautions for use and maintenance?

As a non-resorbable and reusable instrument, the Hu-Friedy knife requires a strict maintenance protocol. Before the first use and after each intervention, the device must be cleaned, disinfected, and sterilized in accordance with the manufacturer's instructions and current hygiene standards. It is imperative to read the instructions carefully before use to comply with the recommended sterilization parameters. Precautions include checking the integrity of the cutting edge to avoid unnecessary tissue trauma. Storage must be in a dry and clean environment to preserve the physical properties of the gold-plated handle and the active part of the instrument.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device according to current regulations. The manufacturer Hu-Friedy is globally recognized for its compliance with quality standards in the production of surgical instruments. Although CE marking is not specifically mentioned in the source data, compliance with US and international regulatory requirements for Class I devices is ensured by the manufacturer's quality control processes. The use of this instrument is strictly regulated and dedicated to dental sector experts.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.