Delynov Endodontic Explorer DG16 Handle #7 Black - Hu-Friedy
The Sonde Endo #DG16 manche #7 noir - 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 Endo Probe #DG16 black #7 handle?
The Endo Probe #DG16 black #7 handle is a manual examination instrument designed by the manufacturer Hu-Friedy. This device belongs to the category of specialized instrumentation for endodontics. Its structure consists of a double active part, specifically sharpened for the detection of anatomical structures, and a black number 7 type handle. This handle is designed to offer an optimal tactile response during intra-canal diagnostic procedures. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the quality requirements of a recognized manufacturer in the field of dental surgery and endodontics.
What are the clinical indications for this instrument?
This endodontic exploration probe is primarily indicated for locating root canal entries after opening the pulp chamber. It allows the practitioner to probe the pulp floor to identify orifices, even when they are calcified or difficult to access. In clinical practice, it is used to evaluate the internal anatomy of the tooth, verify the presence of secondary canals, and guide the insertion of endodontic files. Its use is common during initial endodontic treatments or during complex retreatments requiring meticulous exploration of internal dental structures.
What are the technical characteristics of the Hu-Friedy DG16 probe?
The DG16 probe is distinguished by its tapered and rigid tips, essential for precise exploration without deformation under pressure. The model presented features a black number 7 handle, an ergonomic characteristic specific to the Hu-Friedy range that allows for rapid differentiation within the technical tray. As a Class I device, this instrument is designed to be reusable after an appropriate cleaning and sterilization cycle, in accordance with the protocols in force in dental practices. Its monobloc or assembled design according to the manufacturer's standards guarantees a direct transmission of tactile sensations from the operative field to the practitioner's hand.
What are the contraindications for the use of this probe?
According to data provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for the use of this exploration instrument, other than those related to the patient's general health status not permitting a dental care procedure. However, the use of this instrument is strictly reserved for qualified healthcare professionals. It is imperative not to use the instrument if it shows signs of corrosion, deformation, or wear of the active tips, as this could compromise the accuracy of the endodontic diagnosis or lead to a risk of instrumental fracture.
What are the maintenance precautions for this non-resorbable probe?
As a non-resorbable metallic instrument, the DG16 probe requires a rigorous decontamination and sterilization protocol between each patient. Before the first use and after each intervention, the instrument must be cleaned, disinfected, and sterilized in an autoclave according to the instructions from the manufacturer Hu-Friedy. It is recommended to read the instructions carefully before use to respect the temperature and duration parameters. Particular attention must be paid to drying to avoid any oxidation. Storage must be in a dry and sterile environment to maintain the integrity of the device until its next clinical use.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This product is classified as a Class I medical device. Although the specific CE marking is not detailed in the provided sources, the manufacturer respects the regulatory standards for the marketing of precision surgical instruments. Compliance with Class I requirements implies strict manufacturing control to guarantee the safety and efficacy of the instrument during its intended use in endodontics. Professionals must refer to the labeling and accompanying instructions for any additional information relating to traceability and safety standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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