Luks #4 gutta-percha plugger #32 handle 1.0mm
The Fouloir à gutta Luks #4 manche #32 1,0mm 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.
What is the Luks #4 gutta plugger handle #32 1,0mm?
The Luks #4 gutta plugger from the brand Hu-Friedy is a manual instrument specifically designed for endodontics. This device consists of a working part calibrated at 1,0mm and a #32 type handle offering a grip adapted to precision procedures. Its structure is optimized to transmit the necessary force during the condensation of canal filling materials. Manufactured under the control of the manufacturer Hu-Friedy, this instrument meets the quality requirements for office interventions. The brand Hu-Friedy offers here a reliable tool for practitioners performing complex root treatments requiring rigorous compaction of gutta-percha.
What are the clinical indications?
This manual endo plugger is indicated for the obturation phase of the canal system after shaping and cleaning. It is particularly used in vertical condensation techniques, allowing for the compaction of softened or cold gutta-percha towards the apex and canal walls. The clinical objective is to eliminate voids and ensure a hermetic seal to prevent reinfection. This endo plugger from the brand Hu-Friedy is suitable for large diameter canals or the coronal and middle parts of roots, thanks to its 1,0mm tip. Its use is strictly reserved for healthcare professionals qualified in dental surgery and endodontics.
What are the technical characteristics?
The Luks #4 gutta plugger presents precise technical specifications to meet endodontic standards. It has an active tip of 1,0mm, corresponding to size #4 in the Luks classification. The associated handle is a #32 model, designed to ensure adequate balance during manipulation. As a Class I medical device, it complies with basic regulatory standards for non-invasive or short-term invasive instrumentation. The design by the manufacturer located in Chicago guarantees compliance with rigorous manufacturing protocols. This instrument is delivered non-sterile and must undergo an appropriate cleaning and sterilization cycle before each clinical use.
What are the contraindications for use?
According to information provided by the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for healthcare professionals. Although specific data from the raw MDR text does not list medical contraindications related to systemic pathologies or contact allergies, general principles of endodontics should be respected. Use is contraindicated in canals with a diameter of less than 1,0mm to avoid any risk of root fracture or instrument blockage. It is imperative to read the instructions carefully before use to become aware of all warnings and usage limits defined by the manufacturer.
What are the maintenance and handling precautions?
As this device is non-resorbable, its durability depends on post-operative maintenance. After each intervention, the luks plugger must be cleaned to remove residues of sealing cement or gutta-percha. Precautions include the use of non-corrosive cleaning solutions to preserve the integrity of the 1,0mm tip. Sterilization must be carried out according to the parameters validated by the manufacturer Hu-Friedy for Class I instruments. A visual inspection before each use is recommended to detect any deformation or wear of the active part that could compromise the effectiveness of the condensation or patient safety during endodontic treatment.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-Friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 in the USA. The product is listed under Class I according to medical device regulations. This classification implies that the instrument meets the essential safety and performance requirements for manual surgical tools. As a product distributed under the brand Hu-Friedy, it benefits from the expertise of a globally recognized manufacturer in the dental sector. Practitioners must refer to the instructions provided by the manufacturer to ensure use in accordance with the health and safety standards in force in their jurisdiction.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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