Gracey curette #12/13 smooth handle CC, MF, red
The Curette Gracey #12/13 manche lisse CC, MF, rouge 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 #12/13 curette smooth handle CC, MF, red?
The Gracey #12/13 curette offered by the Hu-Friedy is a precision manual instrument belonging to the INSTRU category. It is distinguished by its smooth handle and its red color code, facilitating its identification in the surgical tray. This Class I medical device is specifically designed for periodontology and oral surgery procedures. The Hu-Friedy relies on the expertise of its official manufacturer located in the USA to offer a tool adapted to clinical requirements. Its structure is designed to allow effective access to difficult anatomical areas, while respecting the surrounding tissues during manual instrumentation.
What are the clinical indications?
The clinical indications for this instrument from the Hu-Friedy mainly concern the treatment of periodontal diseases. The Gracey #12/13 curette is used for the removal of subgingival calculus deposits and root planing, specifically on the distal surfaces of posterior teeth. In implant or periodontal surgery, it allows for the mechanical debridement of surfaces to promote epithelial reattachment or site decontamination. Its use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-friedy, thus guaranteeing an application compliant with current clinical protocols in dental offices or hospital settings.
What are the technical characteristics?
Technically, this curette from the Hu-Friedy is characterized by a specific angulation of its working part, optimized for posterior sectors. The smooth handle offers a direct grip for the practitioner. As a Class I device, it meets essential manufacturing standards for non-invasive or minimally invasive surgical instrumentation. The manufacturer Hu-friedy, based in Chicago, ensures production compliance. The red color code and the MF and CC markings specify its configuration within the INSTRU range, allowing for smooth integration into sterilization protocols and ergonomic organization of complex periodontal care.
What are the contraindications for use?
According to the data provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively beyond general usage warnings. However, the use of this instrument from the Hu-Friedy is exclusively reserved for trained healthcare professionals. Incorrect angulation or excessive pressure could damage the root cementum or soft tissues. It is imperative to read the instructions carefully before use to identify any restrictions related to the patient's clinical condition or the integrity of the instrument. Use must be proscribed if the device shows signs of wear or deformation that could compromise the safety of the treatment.
What are the maintenance and durability precautions?
As a non-resorbable instrument in the INSTRU category, the durability of the Gracey #12/13 curette strictly depends on compliance with cleaning, disinfection, and sterilization protocols. Although material details are not specified, this type of Class I device requires rigorous maintenance to maintain its cutting capabilities. Professionals must follow the instructions of the manufacturer Hu-friedy regarding the product's life cycle. Particular precautions must be taken during sharpening to preserve the original angulation of the blade. A systematic visual inspection before each intervention is recommended to guarantee the effectiveness of the surgical procedure.
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. The Hu-Friedy ensures the distribution of this high-quality instrument intended for oral surgery. Compliance with regulatory requirements is evidenced by the Class I status of the device, guaranteeing rigorous control of manufacturing processes. Practitioners are invited to consult the labeling and instructions for any additional information on safety standards. Compliance with the manufacturer's warnings is essential to ensure patient safety and the clinical performance of the instrument.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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