Gracey curette #13/14 handle #2 AF distal
The Curette Gracey #13/14 manche #2 AF distal 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 curette #13/14 handle #2 AF distal?
The Gracey curette #13/14 handle #2 AF distal from the brand Hu-Friedy is a precision instrument belonging to the INSTRU category. It consists of a specific working end and a #2 AF handle, optimized for interventions in the posterior zone. This medical device is manufactured under the supervision of the manufacturer Hu-friedy, a recognized entity in the instrumentation sector. Its structure is designed to meet the requirements of dental surgeons during periodontal care. As a product of the brand Hu-Friedy, this instrument complies with the rigorous manufacturing standards imposed for Class I devices. Its design focuses on access to difficult areas, ensuring handling adapted to the clinical needs of practitioners.
What are the clinical indications?
This distal periodontal curette is primarily indicated for the mechanical treatment of periodontal diseases. It is used by healthcare professionals for scaling and root planing of the distal surfaces of posterior teeth. Its specific geometry allows for the effective removal of subgingival calculus and necrotic tissue on the root cementum. The use of this instrument from the brand Hu-Friedy is essential during the initial treatment or periodontal maintenance phases. It allows for the cleaning of deep periodontal pockets where access is limited. The main indication remains the preparation of root surfaces to promote epithelial reattachment and the health of supporting tissues.
What are the technical characteristics?
The Gracey curette #13/14 is distinguished by a precise angulation of its shank, designed to reach the distal surfaces of molars. The #2 AF (After Five) handle is characterized by an elongated terminal shank, which facilitates insertion into periodontal pockets exceeding 5mm. This technical specificity allows the practitioner to operate with better visibility and optimal angulation without traumatizing the surrounding soft tissues. This Class I device is a non-motorized manual instrument. The design of the brand Hu-Friedy ensures fine tactile transmission, allowing the surgeon to detect irregularities on the root surface. The #13/14 configuration is a recognized standard in periodontology for the treatment of posterior sectors.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the technical documentation, other than those related to standard oral surgery procedures. Use must comply with the intended use described by the manufacturer. It is imperative to read the instructions carefully before any use to ensure patient safety. As with any periodontal instrument, inappropriate use or use by untrained personnel could result in damage to periodontal tissues or tooth structure. Compliance with sterilization and maintenance protocols is also a sine qua non condition for its clinical use.
What are the precautions for use and maintenance?
As a non-resorbable and reusable instrument, the Gracey curette #13/14 requires a rigorous maintenance protocol. After each distal periodontics intervention, the instrument must be cleaned, disinfected, and sterilized in accordance with the instructions from the manufacturer Hu-friedy. Practitioners must ensure the blade remains sharp to guarantee the effectiveness of the clinical gesture and avoid excessive pressure on the root. Regular sharpening with appropriate stones is recommended to preserve the cutting performance of this instrument from the brand Hu-Friedy. It is advised to visually inspect the instrument before each use to detect any trace of corrosion or deformation that could compromise the safety of the treatment.
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 the regulatory requirements in force for this category of surgical instruments. Although CE marking is not specified in the source data, the product is intended exclusively for professional use within the framework of dental surgery and periodontology. Manufacturing by Hu-friedy guarantees traceability and compliance with industrial standards for manual instruments. Users are invited to systematically refer to the instructions for use provided by the manufacturer to ensure practice in accordance with safety and clinical efficacy standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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