Gutta-percha plugger #5/7 handle #32 0.50-0.75mm
The Fouloir à gutta #5/7 manche #32 0,50-0,75mm 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.
| Manufacturer: Hu-Friedy |
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What is the gutta plugger #5/7 handle #32 0.50-0.75mm?
The gutta plugger #5/7 from the brand Hu-Friedy is a manual instrument designed specifically for endodontic procedures. This device consists of a #32 type handle and two active ends with distinct diameters of 0.50mm and 0.75mm. Its structure is designed to allow the application of axial pressure on obturation materials. As a double endo plugger, it offers immediate versatility to the practitioner during the different stages of condensation. This instrument belongs to the INSTRU category and benefits from the expertise of its recognized manufacturer, Hu-Friedy, based in the United States. It is intended exclusively for professional use in dental offices or hospital environments for endodontic surgery interventions.
What are the clinical indications for this instrument?
The clinical indications for this gutta plugger from the brand Hu-Friedy primarily concern the obturation of root canals. It is used during the vertical condensation phase, whether performed cold or after thermal softening of the gutta-percha. Its design allows for the compaction of the obturation material and root canal cements to eliminate voids and ensure the apical and lateral seal of the canal system. The use of this double endodontic plugger is particularly relevant after canal shaping to ensure that the filling material perfectly matches the anatomical irregularities of the root, thus limiting the risk of post-operative bacterial reinfection.
What are the technical characteristics of this device?
This Class I medical device features precise technical specifications to meet the requirements of modern endodontics. The double endodontic plugger has two working tips: the first end measures 0.50mm in diameter, while the second measures 0.75mm. These dimensions allow for the treatment of canals of various calibres, from the apical third to the coronal third. The #32 handle, developed by the manufacturer Hu-Friedy, ensures a stable grip to transmit the force necessary for condensation without compromising the practitioner's tactile sensitivity. The brand Hu-Friedy guarantees that this instrument complies with rigorous manufacturing standards for non-invasive manual devices used in dentistry.
What are the contraindications for the use of the gutta plugger?
According to information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed outside of those related to standard endodontic protocols. However, the practitioner must ensure that the instrument is used in accordance with its intended use, namely the condensation of obturation materials. Inappropriate use on structures other than gutta-percha or sealing cements could damage the instrument or the tooth walls. It is imperative to read the instructions for use carefully and to respect sterilization protocols before any clinical intervention to ensure patient safety.
What are the precautions for use and maintenance?
As a non-resorbable Class I instrument, the gutta plugger requires rigorous maintenance between each patient. Although composition details are not specified, this type of manual instrumentation must be cleaned, disinfected, and sterilized according to the cycles validated by the manufacturer to prevent cross-contamination. The practitioner must regularly inspect the integrity of the 0.50mm and 0.75mm tips to detect any deformation or signs of wear that could alter compaction precision. Careful handling is recommended to avoid bending the fine tips when inserting them into curved or narrow canals. Compliance with the manufacturer Hu-Friedy's warnings is essential to maintain the tool's longevity.
Who is the manufacturer and what standards are met?
The official manufacturer of this device is Hu-Friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device according to current regulations. It is important to note that CE marking is not specified in the current source data for this specific reference. The brand Hu-Friedy ensures that the distribution of this instrument complies with the requirements of the intended use and the manufacturer's warnings. As a Class I device, it meets the safety and performance standards applicable to manual dental instruments. Professionals should systematically refer to the labeling and the enclosed instructions to confirm specific certifications at the time of purchase.
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