Diamond Tec mesial/distal scaler, #7 blue handle
The Détartreur Diamond Tec mesial/distal, manche #7 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 Diamond Tec mesial/distal scaler?
The Diamond Tec mesial/distal scaler is a precision manual instrument developed by the brand Hu-Friedy for periodontal instrumentation. This device features a #7 blue-colored handle, offering specific ergonomics for prolonged interventions. Its structure is designed to allow optimal access to complex interproximal areas. As a product of the brand Hu-Friedy, it meets the requirements of healthcare professionals seeking reliable tools for the maintenance of tooth supporting tissues. This model combines working ends adapted to mesial and distal surfaces, thus simplifying the technical tray during scaling and root planing sessions.
What are the clinical indications?
The clinical indications for this instrument from the brand Hu-Friedy primarily concern periodontology and prophylaxis. It is indicated for the removal of supra-gingival and sub-gingival calculus, as well as for root debridement. Its specific design allows for effective treatment of mesial scaler areas and difficult-to-access posterior sectors. The use of this distal scaler is particularly recommended during the initial treatment phases of periodontal diseases or during maintenance sessions. This medical device is exclusively reserved for healthcare professionals trained in manual instrumentation techniques, ensuring safe application on cementum and dentin structures.
What are the technical characteristics?
The Diamond Tec mesial/distal scaler presents rigorous technical characteristics. It is equipped with a #7 type handle, recognizable by its blue color, facilitating organization and rapid instrument selection in the practice. The working part benefits from Diamond Tec technology, ensuring a morphology adapted to the anatomical curvatures of the roots. This device is classified as Class I according to medical device regulations. The design allows for precise tactile transmission, essential for detecting residual deposits during root planing. Manufactured under the supervision of Hu-friedy in the USA, this instrument respects strict manufacturing protocols to ensure constant performance in demanding clinical environments.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, specific contraindications are not detailed beyond the intended use. However, the use of this instrument is strictly reserved for qualified healthcare professionals. Improper use or application on non-indicated structures could lead to iatrogenic damage to soft tissues or the tooth surface. It is imperative to read the instructions carefully before use to ensure the compatibility of the care with the patient's clinical state. As with any sharp manual instrument, caution is advised for patients with coagulation disorders or extreme uncontrolled gingival sensitivities.
What are the maintenance and durability precautions?
As a non-resorbable and reusable instrument, the Diamond Tec scaler requires a strict sterilization protocol between each patient. Although composition details are not specified, this type of Class I instrument must be cleaned, disinfected, and sterilized according to current standards in dental surgery. The practitioner must check the integrity of the working ends before each intervention to guarantee the effectiveness of the mesial distal scaler. Normal wear of the cutting edges may occur over time, requiring appropriate sharpening or replacement to maintain clinical precision. Compliance with the sterilization cycles recommended by the manufacturer Hu-friedy ensures the longevity of the device.
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 belongs to the INSTRU category and complies with Class I of the medical device regulations. The Class I designation confirms that the instrument meets the safety and performance requirements for non-invasive or transient use tools. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Every user must consult the accompanying instructions to comply with the usage and safety guidelines established by Hu-friedy, thus ensuring practice in accordance with international standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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