Curvette Vision Curette #13/14 #6 handle

What is the curette curvette vision #13/14 handle #6?

The curette curvette vision #13/14 marketed by the brand Hu-Friedy is a precision instrument intended for periodontal instrumentation. This medical device consists of a specific working part and a #6 type handle, optimized for grip during clinical procedures. Manufactured under the responsibility of the manufacturer Hu-friedy, this vision curette is designed to meet the requirements of dental surgeons and periodontists. Its structure allows for rigorous manipulation during the treatment of root surfaces, ensuring targeted action in difficult-to-access areas. As a Class I device, it complies with manufacturing standards for non-invasive or short-term invasive manual instrumentation.

What are the clinical indications for this instrument?

The use of the curette curvette vision #13/14 from the brand Hu-Friedy is indicated for periodontal debridement procedures, including scaling and root planing (periodontal lithotripsy). It is particularly suitable for treating deep periodontal pockets and furcation areas in posterior sectors. Practitioners use this instrument for the mechanical removal of subgingival calculus and the decontamination of cemental surfaces. Its design is engineered to follow the root anatomy, thus facilitating the removal of inflammatory tissues and bacterial deposits. This instrument is exclusively reserved for healthcare professionals trained in oral surgery and periodontology techniques, in accordance with the manufacturer's directives.

What are the technical characteristics of this device?

The curette curvette vision #13/14 is distinguished by its specific geometry adapted to the distal surfaces of molars and premolars. The #6 handle offers a diameter that promotes tactile control during curettage movements. This device, offered by the brand Hu-Friedy, is a reusable manual instrument that requires a strict sterilization protocol before each use. The design by the manufacturer Hu-friedy guarantees structural integrity compliant with Class I devices. The working ends are sharpened to allow effective cutting while respecting the integrity of the surrounding tissues. The technical reference #13/14 indicates a precise orientation of the blades to cover posterior anatomical sectors with optimal efficiency.

What are the contraindications for the use of this curette?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not exhaustively listed outside of general use warnings. However, the use of the curette curvette vision is contraindicated in patients with known hypersensitivities to the constituent materials of the instrument, although not specified here. It must not be used by unqualified persons, its use being strictly reserved for healthcare professionals. Incorrect angulation or excessive pressure can lead to irreversible damage to the cementum or soft tissues. It is imperative to consult the instructions for use to identify any restrictions related to the patient's clinical state or the nature of the planned intervention.

What are the maintenance and durability precautions?

As it is a non-resorbable and reusable instrument, the curette curvette vision requires rigorous maintenance to maintain its cutting performance. Although the exact composition is not detailed, this type of Class I instrument must be cleaned, disinfected, and sterilized according to current hospital protocols and the instructions of the manufacturer Hu-friedy located in Chicago. Practitioners must regularly inspect the condition of the vision curette blades to detect any signs of wear or corrosion. Periodic sharpening may be necessary to maintain cutting efficiency, while ensuring that the original shape of the working end is not altered. Compliance with these steps guarantees patient safety and the longevity of the Hu-Friedy instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of the curette curvette vision #13/14 is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to the current regulations on medical devices (MDR). The brand Hu-Friedy ensures the distribution of this high-precision instrument. Compliance with Class I indicates that the product meets the essential safety and performance requirements defined for manual surgical instruments. Healthcare professionals must imperatively read the instructions carefully before any use to ensure the conformity of reprocessing procedures and clinical application. No specific mention of CE marking is provided in the current source data.

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