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Luks #3 gutta-percha plugger #32 handle 0.75mm

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The Fouloir à gutta Luks #3 manche #32 0,75mm 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 € Tax Included

51.00 € Tax Included

(0.00 € / Units)
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Instrument

What is the Luks #3 gutta-percha plugger handle #32 0.75mm?

The Luks #3 gutta-percha plugger handle #32 0.75mm from the brand Hu-Friedy is a specific manual instrument used in endodontics. This device consists of a working part calibrated at 0.75mm and an ergonomic handle referenced #32. It is designed for the condensation of gutta-percha inside the canal system after shaping. As an instrument from the brand Hu-Friedy, it meets the requirements of practitioners for the critical steps of obturation. Its structure allows for precise transmission of the compaction force necessary to ensure apical and lateral sealing during complex endodontic treatments.

What are the clinical indications?

The clinical indications for this plugger primarily concern endodontic obturation using the warm or cold vertical condensation technique. This instrument is indicated for compacting gutta-percha cones in the middle and apical third of the root canal. Purchasing an endodontic instrument of this type is essential for dental surgeons performing root treatments where maximum density of the filling material is required. It allows the softened material to be forced into canal irregularities, thus guaranteeing a hermetic seal. Its use is strictly reserved for healthcare professionals trained in conventional and surgical endodontics protocols.

What are the technical characteristics?

The Luks #3 gutta-percha plugger features precise technical characteristics adapted to the canal anatomy. The working part has a diameter of 0.75mm, which allows for intervention in intermediate to wide preparation canals. The #32 handle offers a stable grip for optimal control of the pressure exerted. Manufactured under the supervision of the manufacturer Hu-friedy located in Chicago, this instrument is classified as a Class I medical device. Its design is optimized to withstand the sterilization cycles required in dental offices while maintaining the integrity of its active tip for constant precision during each clinical act.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not detailed beyond the general regulatory framework. However, the use of this instrument is contraindicated for any person who is not a qualified healthcare professional. It must not be used in clinical situations where the root anatomy is incompatible with a diameter of 0.75mm, at the risk of creating ledges or root fractures. It is imperative to read the manufacturer's instructions carefully before use to identify any restrictions related to the canal morphology or the patient's periodontal status that could compromise the success of the endodontic treatment.

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

As it is a manual metallic instrument and not an absorbable device, the precautions for use focus on maintenance and clinical handling. Before each use, the practitioner must check the integrity of the 0.75mm tip of this plugger from the brand Hu-Friedy to ensure the absence of twisting or corrosion. Rigorous cleaning followed by sterilization in accordance with current protocols is mandatory between each patient. During the compaction phase, excessive pressure must be avoided to prevent the risk of root fracture. The instrument must be stored in a dry environment to preserve the mechanical properties of the steel used by the manufacturer.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This Luks #3 gutta-percha plugger is a Class I medical device, respecting the safety and performance standards applicable to this category of dental instruments. The manufacturer emphasizes that this product is exclusively reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, belonging to Class I indicates compliance with basic regulatory requirements for non-invasive or invasive instruments for temporary use. Compliance with the instructions of the manufacturer Hu-friedy is essential to guarantee patient safety.


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Specifications

Manufacturer Hu-Friedy
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