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Gutta-percha plugger #8 handle #32 posterior 0.40mm

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The Fouloir à gutta #8 manche #32 postérieur 0,40mm is a medical device manufactured by le fabricant.

  • Compliance: Medical device Class I.
  • Manufacturer: le fabricant.
  • Reserved for healthcare professionals. Read instructions carefully before use.

51.00 € 51.0 EUR 51.00 €excl. VAT

51.00 €excl. VAT

(0.00 € / Units)
  • Manufacturer

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Instrument
Manufacturer: Hu-Friedy

What is the gutta plugger #8 handle #32 posterior 0,40mm?

The gutta plugger #8 from the brand Hu-Friedy is a manual endodontic instrument specifically designed for root canal obturation procedures. This device consists of a working part with a 0,40mm diameter and an ergonomic handle type #32. Its structure is optimized to transmit controlled pressure on the gutta-percha, thus allowing effective condensation of the material inside the root canal. As a product in the INSTRU category, this instrument meets the requirements of practitioners seeking a reliable tool for the final phases of endodontic treatment. It is a robust device intended for repeated use after appropriate sterilization, guaranteeing precise handling during critical sealing phases.

What are the clinical indications?

This device from the brand Hu-Friedy is indicated for the vertical compaction of gutta-percha after the shaping and cleaning of the root canal system. It is particularly used in posterior sectors where access can be restricted, requiring a specific angulation of the instrument. Its use is essential to eliminate voids within the obturation, thus ensuring a hermetic seal against micro-organisms. Dental surgeons use this 0,40mm plugger to condense filling material in thin or medium-wide canals, whether by lateral or vertical condensation techniques. The clinical objective is to obtain optimal density of the filling material to prevent any peri-apical reinfection.

What are the technical characteristics?

The gutta plugger #8 presents precise technical specifications to meet modern endodontic standards. It features an active tip calibrated at 0,40mm, allowing precise insertion into the majority of canal preparations. The handle #32 offers a stable grip, reducing manual fatigue during the application of condensation force. The design is specifically oriented for posterior use, with a curvature or angulation facilitating the passage of instruments in molar areas. This product is manufactured under the supervision of the manufacturer Hu-friedy, located in Chicago, USA. Its design guarantees axial transmission of force without excessive deformation of the tip, ensuring homogeneous compression of the gutta-percha cones.

What are the contraindications for use?

According to the information provided by the manufacturer, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications include use on non-radicular anatomical structures or for functions other than the compaction of endodontic filling materials. It must not be used if the root canal presents extreme curvatures inaccessible to a 0,40mm instrument without the risk of fracture or the creation of a false canal. It is imperative to consult the instructions before use to become aware of all warnings from the manufacturer Hu-Friedy. Failure to follow sterilization protocols or use by untrained personnel also constitute major contraindications to patient safety.

What are the maintenance and durability precautions?

As this plugger is a non-resorbable Class I instrument, it requires a rigorous cleaning and sterilization protocol between each patient. Before the first use and after each procedure, the practitioner must follow the manufacturer's recommendations to maintain the integrity of the 0,40mm tip. A visual inspection is recommended to detect any trace of corrosion, deformation, or wear of the active tip that could compromise the quality of the compaction. Although robust, excessive pressure or misuse can alter the mechanical properties of the Hu-Friedy brand instrument. Storage must be in a dry and clean environment to preserve the longevity of the handle #32 and its working part.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, whose head office is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product belongs to Class I according to medical device regulations. Compliance with manufacturing standards ensures that the instrument meets safety and performance requirements for endodontic surgery procedures. It is essential that the user carefully reads the instructions provided by Hu-Friedy before any manipulation. As a Class I device, it is designed to offer constant reliability in a demanding clinical environment, provided it is used in accordance with the manufacturer's indications for healthcare professionals.


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