Gracey curette #12/13 #6 AF handle mesial/distal
The Curette Gracey #12/13 manche #6 AF mésial/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 #12/13 handle #6 AF curette?
The Gracey #12/13 handle #6 AF curette from the brand Hu-Friedy is a precision manual instrument belonging to the INSTRU category. This Class I medical device is specifically configured for access to root surfaces. Its structure includes a number 6 AF (After Five) handle associated with a double mesial and distal working end. This instrument from the brand Hu-Friedy is designed to meet the requirements of clinical periodontology interventions. Manufactured under the supervision of the manufacturer Hu-friedy, this tool allows for a rigorous approach to dental hard tissues during periodontal debridement phases in specialized practices or hospital environments.
What are the clinical indications?
The clinical indications for this instrument from the brand Hu-Friedy primarily concern the treatment of periodontal diseases. The Gracey #12/13 curette is indicated for scaling and root planing of the mesial and distal surfaces of posterior teeth. It allows for the effective removal of subgingival calculus and infected cementum, thus promoting tissue reattachment. Its use is strictly reserved for healthcare professionals qualified in oral surgery and periodontology. According to information from the manufacturer Hu-friedy, the instrument must be used in accordance with established clinical protocols for the treatment of deep periodontal pockets, respecting the indications and contraindications mentioned in the technical documentation.
What are the technical characteristics?
The Gracey #12/13 curette is distinguished by its AF (After Five) configuration, optimized for access to periodontal pockets deeper than 5 mm. The #6 handle offers a grip adapted to long-duration procedures. As a Class I device, this instrument meets the rigorous manufacturing standards imposed by the manufacturer Hu-friedy, based in Chicago, USA. The specific mesial/distal design allows for the treatment of several surfaces with a single instrument, thereby reducing the number of manipulations during planing. The quality of the materials used by the brand Hu-Friedy guarantees the resistance necessary for repeated sterilization cycles, essential for maintaining asepsis in dental surgery.
What are the contraindications for use?
In accordance with the data provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively beyond the intended use. However, the use of this instrument from the brand Hu-Friedy is strictly reserved for trained healthcare professionals. Incorrect blade angulation or excessive pressure can lead to irreversible damage to the root surface or surrounding soft tissues. It is imperative not to use the instrument on tissues presenting pathologies incompatible with mechanical periodontal treatment. Practitioners must carefully consult the manufacturer's instructions and warnings before any intervention to ensure patient safety.
What are the maintenance and durability precautions?
As a non-resorbable instrument in the INSTRU category, the durability of the Gracey #12/13 curette depends directly on the maintenance protocols applied. Like any Class I device from the brand Hu-Friedy, it must undergo a complete cycle of cleaning, disinfection, and sterilization between each patient. It is crucial to check the integrity of the working end before each use. Sharpening must be performed by competent personnel to maintain the specific cutting angle of Gracey curettes without altering the steel geometry. Compliance with the manufacturer Hu-friedy's recommendations regarding decontamination products is essential to prevent corrosion and ensure the longevity of the instrument.
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, complying with the current regulatory requirements for reusable manual surgical instruments. The brand Hu-Friedy ensures the distribution of this instrument intended exclusively for healthcare professionals. Although specific CE marking is not mentioned in the source data, compliance with American and international manufacturing standards is ensured by the manufacturer. Users are reminded to carefully read the instructions for use and respect the warnings provided by Hu-friedy to ensure safe use in compliance with the MDR.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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