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Hachette Number 15/16 DE (15-8-14) with Number 9 handle - Hu-Friedy - Delynov

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The Sonde Endo #DG16, Black Line - 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.

fabricant : Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA . Réservé aux professionnels de santé. Lire attentivement la notice avant utilisation.

54.75 € 54.75 EUR 54.75 € Tax Included

54.75 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Endo #DG16 Black Line probe?

The Endo #DG16 probe from the Black Line range, designed by Hu-Friedy, is a precision manual instrument intended for endodontic procedures. This high-quality medical device is distinguished by its Black Line finish, offering optimal visual contrast during clinical procedures. As a diagnostic and localization instrument, this probe facilitates the practitioner's work in identifying canal orifices. Hu-Friedy, a world-renowned manufacturer, ensures an ergonomic design to meet the requirements of dental health professionals. This product belongs to the category of consumables and diagnostic instruments for dental surgery and endodontics.

What are the clinical indications for this instrument?

The intended use of the Hu-Friedy Endo #DG16 Black Line probe is strictly reserved for qualified healthcare professionals, notably dental surgeons and endodontists. It is primarily indicated for the localization and exploration of root canal entries during initial endodontic treatments or retreatments. Thanks to its fineness and rigidity, it allows for precise tactile detection of canal orifices, even in conditions of reduced visibility. Its use is part of a rigorous clinical framework where instrumental precision is essential for the success of canal therapy.

What are the technical characteristics of the Endo #DG16 probe?

The Endo #DG16 Black Line probe benefits from the expertise of Hu-Friedy Mfg. Co., LLC in metallurgy and ergonomic design. Although specific details of the composition are not detailed in the raw technical documentation, the Black Line range is recognized for its dark finish which reduces reflections under operating lights, thereby improving the visual comfort of the surgeon. This instrument is designed to offer excellent tactile sensitivity, allowing for the distinction of dentinal structures. It is a robust device, adapted to standard sterilization protocols used in dental practices, guaranteeing longevity in accordance with the brand's standards.

What are the contraindications for the use of this device?

According to the warnings from the manufacturer Hu-Friedy, the use of this instrument is exclusively reserved for healthcare professionals. Contraindications include any use diverted from its intended use, namely endodontic exploration. It must not be used by untrained personnel or for non-dental surgical applications. The practitioner must ensure the integrity of the instrument before each use. Any deformation or excessive wear of the probe tip can compromise diagnostic precision or risk instrumental fracture, thus constituting a contraindication to its immediate use.

What are the precautions for use and maintenance?

To guarantee patient safety and the durability of the Endo #DG16 Black Line probe, professionals must imperatively read the instructions carefully before use. Like any Class I instrument, it requires a rigorous cleaning, disinfection, and sterilization protocol between each patient to prevent risks of cross-contamination. It is advised to regularly inspect the probe tip to check for the absence of corrosion or metal fatigue. Compliance with the maintenance instructions from Hu-Friedy Mfg. Co., LLC allows for the preservation of the mechanical properties and the visual appearance of the Black Line finish over the long term.

Who is the manufacturer and what standards are met?

The Endo #DG16 Black Line probe is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a Hu-Friedy product, it meets the high manufacturing standards imposed by the brand for surgical and endodontic instruments. Practitioners can refer to the indications and warnings provided by the manufacturer to ensure use in compliance with safety and performance requirements. Although specific CE marking is not mentioned in the source data, the product complies with the conformity protocols applicable to medical devices of its class.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Hu-Friedy
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