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DG16 Endodontic Explorer with #6 Handle - Hu-Friedy

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The Sonde exploratrice endodontique DG16 avec manche #6 - 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.

47.10 € 47.1 EUR 47.10 € Tax Included

47.10 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy DG16 endodontic explorer probe?

The DG16 endo explorer probe is a manual diagnostic instrument specifically designed for endodontics. Manufactured by Hu-Friedy Mfg. Co., LLC, this probe is distinguished by its double-ended configuration, optimized for searching for canal orifices. The model presented here is equipped with the #6 handle, a handle with a wider diameter than classic standards, aimed at modifying the instrument's grip during delicate phases of pulp chamber exploration. As a Class I medical device, this instrument meets the basic regulatory requirements for non-invasive or short-term invasive dental instrumentation.

What are the clinical indications for this instrument?

The use of the Hu-Friedy DG16 probe is indicated during initial endodontic treatments or retreatments. Its primary role is the localization of root canal entries after opening the pulp chamber. It allows the practitioner to detect canal orifices, evaluate their orientation, and check for the absence of calcified obstructions at the canal entrance. This instrument is essential for mapping complex endodontic anatomy, helping to secure the subsequent steps of canal scouting and shaping. It is used exclusively by health professionals qualified in dental surgery and endodontics.

What are the technical characteristics of the #6 handle?

The Hu-Friedy DG16 probe is mounted on a #6 type handle. This handle is characterized by an increased diameter compared to traditional handles like the #4. This technical specificity influences the handling dynamics of the instrument in the hand, offering a larger contact surface for the practitioner's fingers. The instrument design by Hu-Friedy Mfg. Co., LLC ensures a smooth transition between the handle and the working ends of the endo explorer probe. The metallic structure of the instrument is designed to withstand the sterilization cycles required in dental offices, in accordance with standard hygiene protocols for Class I devices.

What are the contraindications for using the DG16 probe?

According to information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond the intended use by healthcare professionals. Generally, the use of this instrument is contraindicated for any application other than the endodontic exploration for which it was designed. It must not be used as a lever or for forceful tasks that could lead to the fracture of the fine tips. Practitioners must refer to the instructions for use before any handling. As with any metallic instrument, vigilance is necessary in patients with known sensitivities to the alloy components, although not specified here.

What are the precautions for use and maintenance for this device?

Since the DG16 probe is a non-resorbable and reusable instrument, it requires a strict protocol of cleaning, disinfection, and sterilization between each patient. Before the first use and after each intervention, the practitioner must carefully read the instructions. It is appropriate to visually inspect the integrity of the explorer tips to ensure they are neither dull nor bent, which would impair the precision of canal localization. Although the exact material is not listed, maintenance must follow standard Hu-Friedy recommendations for Class I instrumentation to prevent corrosion and maintain the diagnostic performance of the endo explorer probe.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618 USA. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its instrumentation. This product is classified as a Class I medical device. Compliance with this regulatory class implies that the instrument meets the safety and performance standards defined for this category of devices. It is reminded that this equipment is strictly reserved for healthcare professionals. As the CE marking is not specified in the source data, the product labeling should be checked to confirm applicable regional certifications at the time of purchase.


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Manufacturer Hu-Friedy
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