Gracey Turgeon curette #11/12 modified #6 handle
The Curette Gracey Turgeon #11/12 manche #6 modifiée is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Gracey Turgeon #11/12 modified #6 handle curette?
The Gracey Turgeon #11/12 modified #6 handle curette, offered by the brand Hu-Friedy, is a specialized manual instrument belonging to the INSTRU category. This device is distinguished by its specific configuration intended for the treatment of periodontal tissues. It features a number 6 handle, providing a grip adapted to the requirements of oral surgery. As an instrument from the brand Hu-Friedy, it meets the needs of practitioners seeking tools dedicated to the removal of tartaric deposits and the smoothing of root surfaces. Its modified structure is designed to optimize angulation during insertion into precise anatomical sites, thus ensuring a targeted intervention on the concerned dental structures.
What are the clinical indications for this instrument?
The clinical indications for the Hu-Friedy Gracey Turgeon #11/12 curette primarily concern the treatment of periodontopathies. It is indicated for the scaling and root planing of the mesial surfaces of posterior teeth, notably premolars and molars. This instrument is used by healthcare professionals to eliminate subgingival tartar and necrotic tissues from the cemental wall. Its use is reserved for clinical periodontology interventions and implant or dental maintenance. The manufacturer Hu-friedy specifies that this device is exclusively reserved for trained healthcare professionals, guaranteeing a safe application compliant with current therapeutic protocols in dental and oral surgery.
What are the technical characteristics of the curette?
Technically, the Gracey Turgeon #11/12 curette is characterized by a working part that is modified compared to the standard Gracey model, facilitating access to difficult areas. It is mounted on a #6 handle, a classic format allowing precise tactile control during the removal of calcified deposits. This medical device belongs to Class I according to current regulations. Although specific material details are not provided, this INSTRU category instrument is designed to withstand standard sterilization cycles in the practice. The technical reference indicates manufacturing under the supervision of the manufacturer Hu-friedy, located in Chicago, guaranteeing compliance with manufacturing standards for precision manual instruments.
What are the contraindications for the use of this device?
According to information provided by the manufacturer Hu-friedy, specific contraindications are not exhaustively listed beyond general warnings. However, the use of this instrument is strictly reserved for qualified healthcare professionals. This curette should not be used outside of its intended use, namely periodontal treatment. Inappropriate use on fragile prosthetic restorations or non-compatible materials could compromise the integrity of the instrument or the treated surface. It is imperative to read the instructions carefully before any use to ensure the absence of patient-specific clinical contraindications, such as undocumented hypersensitivities or local tissue conditions contraindicating mechanical debridement.
What are the precautions for use and maintenance?
As a Class I non-resorbable instrument, the Gracey Turgeon #11/12 curette requires a rigorous decontamination and sterilization protocol after each use. Professionals must inspect the instrument before use to ensure the sharpness of the blade and the absence of corrosion. As it is a manual device, excessive pressure must be avoided to prevent any risk of fracture of the working tip or damage to periodontal tissues. Compliance with the manufacturer Hu-friedy's instructions regarding cleaning and maintenance is essential to preserve the instrument's performance. Handling must be carried out with care by trained personnel to ensure patient safety and the longevity of the Hu-Friedy product.
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 is classified as a Class I medical device, meeting basic regulatory requirements for non-invasive or short-term invasive surgical instruments. Although specific CE marking is not mentioned in the source data, the manufacturer follows American and international manufacturing guidelines for healthcare devices. The curette is distributed under the brand Hu-Friedy, ensuring traceability and compliance with the provided indications. It is reminded that this equipment is exclusively reserved for healthcare professionals and that a careful reading of the instructions for use is mandatory before any clinical intervention.
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Specifications
| Manufacturer | Hu-Friedy |
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