Gracey curette #13/14 handle #7 distal blue
The Curette Gracey #13/14 manche #7 distal bleu 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 #7 distal blue?
The Gracey Curette #13/14 handle #7 distal blue, offered by the brand Hu-Friedy, is a manual instrument specific to periodontology. It consists of a #7 type handle and a double working end designed to access difficult areas of the posterior sector. This medical device is manufactured under the responsibility of Hu-friedy and belongs to the category of periodontal diagnostic and treatment instruments. As a distal dental curette, it features a precise angular inclination that allows for optimal adaptation to the roots of posterior teeth. This product from the brand Hu-Friedy is intended exclusively for professional use in dental offices or hospital environments for prophylaxis and support tissue care interventions.
What are the clinical indications?
This scaling curette is specifically indicated for root planing and subgingival scaling of the distal surfaces of premolars and molars. In periodontal surgery, it is used for the debridement of deep periodontal pockets where access is limited. The instrument allows for effective removal of calculus and biofilm while preserving the integrity of the surrounding soft tissues. The design of the gracey 13-14 curette ensures a correct working angle relative to the root surface, which is crucial for achieving a smooth surface after treatment. The use of this instrument from the brand Hu-Friedy is reserved for qualified healthcare professionals practicing periodontics or oral surgery.
What are the technical characteristics?
The gracey 13-14 curette is distinguished by its angled morphology, specifically studied for distal areas. It has a number 7 handle, identified by a blue color code, facilitating its organization within the procedural tray. This device is classified as Class I according to medical device regulations. The working part is designed to offer a unique sharp blade on a single edge, a characteristic specific to Gracey-type curettes, allowing for selective work on the root without damaging the opposite gingiva. Manufactured by Hu-friedy in the USA, this instrument meets the rigorous requirements of daily clinical practice in periodontology and implantology.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, the indications and contraindications are related to the intended use of the instrument. Although no specific medical contraindications are listed in the raw documentation, the use of this distal periodontal curette should be avoided on tissues presenting uncontrolled acute inflammation without an adapted protocol, or in patients presenting unevaluated systemic fragilities. It is imperative that the practitioner consults the instructions before use to ensure patient safety. The instrument must not be used for functions other than those for which it was designed, such as the extraction of posts or work on hard restorative materials that could damage the blade.
What are the maintenance and handling precautions?
As a non-resorbable and reusable Class I instrument, this curette requires a strict sterilization protocol between each patient. Although composition details are not specified, handling must be performed with care to maintain the sharpness of the distal dental blade. The practitioner must ensure to inspect the instrument before each use to detect any trace of wear or corrosion. Being a device reserved for healthcare professionals, it must be handled in accordance with current good hygiene and safety practices. Regular sharpening by trained personnel is recommended to guarantee clinical efficacy during scaling and root planing.
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 Class I in accordance with medical device regulations. The manufacturer specifies that the use of this instrument is strictly reserved for healthcare professionals. It is essential to read the provided instructions for use carefully to respect all warnings and safety procedures. Although CE marking is not specified in the source data, compliance with Hu-friedy manufacturing standards ensures the practitioner an instrument meeting professional requirements for periodontal care and dental surgery interventions.
State of the art
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Specifications
| Manufacturer | Hu-Friedy |
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