Gracey curette #215/216 handle #7 mini yellow

What is the Gracey curette #215/216 handle #7 mini yellow?

The Gracey curette #215/216 handle #7 mini yellow marketed by the Hu-Friedy is a specific manual instrument belonging to the INSTRU category. This device is distinguished by its 'mini' type termination, designed to intervene in restricted periodontal spaces where standard curettes might be limited by their bulk. It is equipped with a number 7 handle, identified by a yellow color code, facilitating its organization within the technical tray. This Class I equipment is manufactured by Hu-friedy in the United States and meets the quality requirements for manual instrumentation in dental surgery and periodontology. The Hu-Friedy offers this tool for practitioners seeking a fine periodontal curette adapted to complex root anatomies.

What are the clinical indications?

The clinical indications for this instrument from the Hu-Friedy primarily concern the treatment of periodontal diseases. As a gracey mini curette, it is recommended for root debridement and planing in deep and narrow periodontal pockets. Its geometry is specifically studied to adapt to root surfaces, allowing for precise removal of subgingival tartar and necrotic tissues. It is used by dental surgeons, periodontists, and hygienists as part of initial therapies or periodontal maintenance. The intended use, as defined by the manufacturer Hu-friedy, is strictly reserved for qualified healthcare professionals mastering specific manual instrumentation techniques.

What are the technical characteristics?

The Gracey curette #215/216 is characterized by a working part that is refined compared to standard models, making it a fine periodontal curette ideal for difficult access areas. The #7 handle offers a diameter and texture adapted to ensure optimal control during the traction movements necessary for planing. The yellow color code allows for quick visual identification during interventions. This Class I medical device is designed to withstand the cleaning and sterilization cycles required in a dental office. As an instrument from the manufacturer Hu-friedy, it benefits from recognized expertise in the design of sharp tools for periodontology, guaranteeing constant cutting efficiency on cemental surfaces.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively, but use is strictly reserved for healthcare professionals. Generally, in periodontology, the use of this instrument from the Hu-Friedy could be contraindicated in patients presenting with serious systemic conditions that do not allow for invasive dental care or in cases of unmanaged dentinal hypersensitivity. It is imperative to read the instructions carefully before use to ensure the conformity of the clinical gesture with the manufacturer's recommendations. Use by unqualified personnel is formally prohibited to avoid any damage to the soft tissues or the patient's root surface.

What are the maintenance and durability precautions?

As a non-resorbable and reusable instrument, the Gracey curette #215/216 requires a rigorous maintenance protocol. Although composition details are not specified, this type of Class I instrument must be cleaned, disinfected, and sterilized before each use in accordance with current hygiene protocols. It is essential to check the integrity of the working part and the sharpness of the blade before each procedure. Regular sharpening, performed with appropriate stones, may be necessary to maintain the cutting performance of this fine periodontal curette. Compliance with the maintenance instructions from the manufacturer Hu-friedy guarantees the longevity of the instrument and patient safety during periodontal care.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product belongs to Class I according to medical device regulations. The Hu-Friedy ensures the distribution of this instrument intended exclusively for healthcare professionals. Although specific CE marking is not mentioned in the source data, the product meets the manufacturing standards of a globally recognized manufacturer in the dental sector. Practitioners must refer to the labeling and instructions for use to confirm applicable certifications. The mention 'Class I' confirms its status as a regulated medical device, implying compliance with safety and performance requirements for manual instrumentation.

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