Prophylactic curette #7/8 handle #2
The Curette prophylactique #7/8 manche #2 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 #7/8 prophylactic curette with #2 handle?
The #7/8 prophylactic curette with #2 handle is a specialized manual instrument used in dentistry and periodontology. Developed by the Hu-Friedy brand, this curette is specifically designed for prophylaxis interventions. It consists of a working part numbered 7/8, adapted to precise anatomical areas, and a #2 type handle offering a grip adapted to the requirements of practitioners. This Class I medical device is a precision tool intended for the maintenance of periodontal tissues and the removal of tartar deposits. Its design meets the needs of healthcare professionals seeking reliable instruments for their hygiene and maintenance protocols within their practice.
What are the clinical indications?
The clinical indications for this Hu-Friedy brand instrument primarily concern prophylaxis and non-surgical periodontics procedures. The prophylactic curette is indicated for the removal of supra-gingival and sub-gingival tartar, as well as for root planing. It is particularly useful during periodontal maintenance sessions to debride pockets and sanitize cementum surfaces. In oral and implant surgery, it can be used to prepare the surgical site or maintain hygiene around peri-implant tissues. The use of this curette is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-friedy, to guarantee a safe and effective therapeutic application during routine or complex dental care.
What are the technical characteristics?
The prophylactic curette is distinguished by its #7/8 technical configuration, a standardized nomenclature that defines the angulation and shape of its active ends to effectively reach target surfaces. The #2 handle is designed to ensure controlled manipulation during curettage movements. This device is classified as a Class I instrument according to the medical device regulations (MDR). Manufactured under the supervision of Hu-friedy, this Hu-Friedy brand instrument respects rigorous manufacturing standards. Although specific material details are not listed, the structure of the instrument is optimized to withstand the sterilization cycles necessary in a clinical environment while maintaining its cutting capabilities for repeated prophylaxis procedures.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, specific contraindications related to the use of the prophylactic curette are not detailed beyond general warnings. However, the use of this instrument is formally reserved for duly trained healthcare professionals. It is imperative to read the instructions carefully before any use to identify possible usage restrictions related to the patient's clinical state or the nature of the treated tissues. As with any prophylaxis instrument, inappropriate use by unqualified personnel constitutes a major contraindication. The practitioner must evaluate the relevance of manual instrumentation in relation to the patient's periodontal status and any gingival or dentinal sensitivities encountered during care.
What are the maintenance and handling precautions?
As a non-resorbable and reusable instrument, the Hu-Friedy brand prophylactic curette requires a strict decontamination and sterilization protocol after each use. Professionals must follow the recommendations of Hu-friedy located in Chicago, USA, to guarantee the longevity of the instrument and patient safety. It is essential to check the integrity of the #7/8 working part before each intervention. Any deformation or excessive wear of the cutting edges can compromise scaling efficiency and requires sharpening or replacement. Handling must be precise to avoid any damage to surrounding soft tissues. Compliance with the recommended cleaning cycles for Class I devices is indispensable to maintain the mechanical properties of the #2 handle and the active ends.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is marketed under the Hu-Friedy brand and belongs to the INSTRU category. As a Class I device, it meets the regulatory requirements in force for manual surgical and dental instruments. Compliance with manufacturing standards is ensured by the manufacturer, guaranteeing that the instrument is suitable for professional use in a dental office or hospital environment. Practitioners are invited to consult the attached instructions for use to become aware of all warnings and maintenance procedures recommended by Hu-friedy in order to guarantee use in accordance with regulatory marking and current safety standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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