Endodontic Microprobe Sonde Abou-Rass Number 5 Handle 40 - Hu-Friedy - Delynov
The Sonde micro-endo Abou-Rass #5 manche 40 - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Hu-Friedy Abou-Rass #5 micro-endo probe?
The Abou-Rass #5 micro-endo probe, associated with the 40 handle, is a specialized exploration instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed to meet the requirements of micro-endodontics. Its fine structure and particular configuration allow for a precise approach to hard-to-reach areas within the canal system. As a diagnostic and exploration instrument, this dental micro-probe is integrated into endodontic surgery protocols where visibility and delicacy of intervention are crucial. It benefits from the manufacturing expertise of Hu-Friedy, guaranteeing a tool adapted to the constraints of daily clinical practice in dental offices or hospital settings.
What are the clinical indications for this dental micro-probe?
The Abou-Rass probe is primarily indicated during the exploration phases of surgical and conventional endodontics. It is used for detecting calcified canals, locating canal entries, and examining isthmuses between two canals. In apical surgery, this micro-endo probe allows for checking the cleanliness of the a retro preparation and ensuring the absence of debris or residual filling materials. Its use is essential for mapping the internal root anatomy under optical aid, such as an operating microscope or high-magnification loupes. It thus helps the practitioner to secure the cleaning and shaping stages of the canal system during complex treatments.
What are the technical characteristics of the Abou-Rass #5 canalization probe?
The Abou-Rass #5 canalization probe is distinguished by its design optimized for micro-surgery. It is mounted on a 40 handle specific to the Hu-Friedy range, offering a grip adapted to precision movements. Although exact dimensions are not specified, the Abou-Rass range is recognized for the fineness of its working ends, allowing for intervention without obstructing the visual field under a microscope. This instrument belongs to the INSTRU category and is classified as a Class I device according to current regulations. The manufacturing quality of Hu-Friedy Mfg. Co., LLC ensures the mechanical resistance necessary for the stresses encountered during the exploration of hard canal walls, while maintaining the tactile sensitivity indispensable to the practitioner.
What are the contraindications for the use of this endodontic instrument?
According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond general warnings related to professional use. Generally speaking, the use of this endodontic probe is contraindicated in patients with known allergies to the metallic components of the instrument, although the exact composition is not specified here. It is imperative not to use the instrument for tasks for which it is not intended, such as elevating bone structures or applying excessive leverage forces that could lead to a fracture of the fine tip. The practitioner must systematically refer to the instructions for use provided by the manufacturer to identify any usage restrictions related to the patient's clinical background.
What are the maintenance and handling precautions?
The Abou-Rass #5 micro-endo probe is a non-absorbable and reusable instrument that requires a strict sterilization protocol before each use. Being a Class I device, it must be handled with care to preserve the integrity of its fine tip. Cleaning must be performed with appropriate detergent and disinfectant solutions, avoiding corrosive agents that could alter the surface condition. After cleaning, thorough rinsing and meticulous drying are necessary before autoclaving. It is recommended to visually inspect the probe under magnification to detect any trace of corrosion, bending, or dulling of the tip, which could compromise the accuracy of the clinical diagnosis or patient safety during the surgical act.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is listed under Class I, which corresponds to medical devices presenting a low degree of risk according to regulatory classification. Although specific CE marking is not mentioned in the source data, Hu-Friedy is a globally recognized manufacturer for compliance with quality standards in the production of surgical instruments. The use of this instrument is strictly reserved for qualified healthcare professionals. Users are reminded to carefully read the instructions for use and warnings provided by Hu-Friedy before any clinical implementation in order to ensure optimal safety.
State of the art
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Specifications
| Manufacturer | Hu-Friedy |
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