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What is the Dr. Wise periotome, Black Line - Hu-Friedy?

The Dr. Wise periotome, part of the Black Line range from the Hu-Friedy brand, is a precision surgical instrument designed for oral surgery procedures. This device, manufactured by Hu-Friedy Mfg. Co., LLC, is specifically developed to meet the requirements of healthcare professionals. As an instrument in the CONSO category, it is part of the specialized tool catalog distributed by Delynov. This model stands out for its ergonomic design and Black Line finish, emblematic features of Hu-Friedy's expertise in high-end dental instrumentation. Its use is strictly reserved for qualified practitioners working in sterile clinical environments.

What are the clinical indications for this Hu-Friedy instrument?

The clinical indications for the Hu-Friedy Dr. Wise periotome primarily concern oral and implant surgery procedures requiring delicate tissue manipulation. According to information from the manufacturer, Hu-Friedy Mfg. Co., LLC, this instrument is intended for healthcare professionals for specific interventions where precision is paramount. Although precise operative details are not exhaustive in the technical documentation, its intended use falls within standard surgical dentistry protocols. It is essential that the user refers to current clinical protocols and the instructions for use to ensure an application consistent with the patient's needs during the surgical act.

What are the technical characteristics of the Dr. Wise periotome?

The Dr. Wise periotome, Black Line - Hu-Friedy features technical characteristics specific to Class I instruments. Developed by Hu-Friedy, this device benefits from advanced engineering located in Chicago, USA. The Black Line range is recognized for offering optimal performance during critical phases of the intervention. As a Class I device, it meets the basic regulatory requirements for non-invasive or reusable surgical instruments depending on the context. The technical reference of this instrument ensures compatibility with the high standards of modern dental surgery, thus guaranteeing the practitioner a reliable tool for daily procedures in the office or hospital setting.

What are the contraindications for the use of this device?

The contraindications relative to the Hu-Friedy Dr. Wise periotome are linked to compliance with safety protocols and the user's skills. According to warnings from the manufacturer Hu-Friedy Mfg. Co., LLC, this instrument is exclusively reserved for duly trained healthcare professionals. Its use by unqualified persons is strictly prohibited. There are no specific contraindications listed beyond those inherent to standard oral surgical procedures. However, the practitioner must imperatively read the instructions carefully before any use to identify possible restrictions related to the patient's physiological state or the nature of the planned intervention.

What are the precautions for use and maintenance?

Precautions for use for the Hu-Friedy Dr. Wise Black Line periotome rely on rigorous handling by healthcare professionals. Like any precision surgical instrument, it requires special attention during handling to preserve the integrity of its active tips. The manufacturer, Hu-Friedy, emphasizes the importance of following the instructions provided in the instructions for use. Although reprocessing details are not specified here, Class I standards generally involve sterilization and cleaning cycles compliant with hospital standards. A visual check before each act is recommended to ensure the perfect condition of the instrument and its optimal functionality.

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. The Dr. Wise periotome is classified as a Class I medical device. This classification attests to its compliance with the regulatory requirements applicable to this category of instruments. The Hu-Friedy brand is globally recognized for its commitment to quality and innovation in the dental sector. Healthcare professionals using this product can refer to the indications and warnings provided by the American manufacturer to ensure safe practice. It is reminded that a careful reading of the instructions is mandatory before any clinical implementation.

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