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Langer Curette number 1/2 with handle number 6 AF - Hu-Friedy - Delynov

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The Fouloir chirurgie endo #1 manche #41 droit - 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.

84.30 € 84.3 EUR 84.30 € Tax Included

84.30 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy endo surgery plugger #1 straight #41 handle?

The endo surgery plugger #1 with straight #41 handle is a manual instrument developed by Hu-Friedy Mfg. Co., LLC for specialized endodontic procedures. This device consists of a straight working part and an ergonomic #41 type handle, facilitating grip during critical surgery phases. As a precision instrument, it is used by specialists to manipulate and condense filling materials. This product belongs to the category of endodontic surgery instruments and benefits from the expertise of a recognized manufacturer in the field of medical instrumentation. Its design meets the requirements of daily clinical practice in dental offices or hospital settings.

What are the clinical indications for this instrument?

This instrument is primarily indicated for endodontic surgery procedures, particularly when a retrograde obturation instrument is required. It is used to compact obturation materials (such as MTA or bioceramic cements) after an apical resection. The straight endo plugger is particularly useful for ensuring apical seal by exerting controlled pressure on the retro-obturation material. Its use is strictly reserved for qualified healthcare professionals, such as endodontists and oral surgeons, involved in complex root treatments or conventional endodontic treatment failures requiring a surgical approach.

What are the technical characteristics of this device?

The Hu-Friedy endo surgery plugger #1 is distinguished by its #41 handle and its straight tip. The Hu-Friedy brand uses rigorous manufacturing standards to guarantee instrument reliability during sterilization cycles and clinical use. The working part is calibrated to allow optimal access to a-retro preparation areas. This device is classified as a Class I instrument according to current regulations. The structure of the #41 handle offers a specific balance allowing high tactile control, essential for assessing the density of the obturation material condensation without exerting excessive stress on the surrounding root structures.

What are the contraindications for the use of this plugger?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, contraindications are related to the intended use and general safety warnings. The use of this instrument is prohibited outside of the healthcare professional framework. It must not be used if the practitioner has not mastered retrograde endodontic surgery techniques. Although the specific material is not detailed here, standard precautions regarding metallic instruments in case of known patient hypersensitivity must be respected. It is imperative to refer to the instructions for use and verify the integrity of the instrument before any intervention to avoid any risk of clinical complication.

What are the maintenance precautions for this non-absorbable instrument?

As a reusable and non-absorbable surgical instrument, the Hu-Friedy plugger must undergo a strict cleaning, disinfection, and sterilization protocol after each use. Healthcare professionals must carefully read the instructions before use to comply with the cycles recommended by the manufacturer. Maintaining the surface condition of the #41 handle and the straight tip is essential to guarantee the tool's longevity and prevent corrosion. Regular visual inspection is recommended to detect any wear or deformation of the working part that could compromise the effectiveness of the retro-obturation instrument during condensation phases.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is a Class I medical device. The Hu-Friedy brand is globally recognized for the quality of its surgical instruments. Compliance with Class I indicates that the device meets the basic regulatory requirements for non-invasive or invasive instruments for temporary use. Practitioners must ensure they consult the instructions and warnings provided by the manufacturer to guarantee use in accordance with the safety and efficacy standards in force in the medical and dental sector.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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