Gutta-percha plugger #11 handle #32 posterior 1.05mm
The Fouloir à gutta #11 manche #32 postér 1,05mm 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 #11 gutta-percha plugger with #32 handle?
The #11 gutta-percha plugger with #32 handle, offered by the brand Hu-Friedy, is a manual instrument used in endodontics for the canal obturation phase. This device consists of a #32 type handle and a working part calibrated at 1.05mm, specifically oriented for use in the posterior sectors of the oral cavity. Designed by the manufacturer Hu-friedy, this instrument is intended for the vertical condensation of obturation material. As a Class I device, it meets the regulatory requirements for reusable non-invasive instruments. Its structure allows for precise transmission of force during gutta-percha compaction, thus ensuring a homogeneous application of the material within the canal system.
What are the clinical indications?
The use of this instrument from the brand Hu-Friedy is indicated during endodontic treatments, specifically for the obturation of root canals. It is particularly recommended for the vertical condensation technique, allowing the compaction of gutta-percha to hermetically seal the apex and lateral canals. Its posterior configuration is adapted for molars and premolars where access is restricted. The practitioner uses this plugger to exert apical pressure on the softened material or gutta-percha cones, ensuring perfect adaptation to the dentinal walls. This endo plugger purchase is reserved exclusively for healthcare professionals trained in dental surgery and endodontic protocols.
What are the technical characteristics?
The #11 gutta-percha plugger features precise technical specifications to meet the needs of endodontists. It has an active tip with a diameter of 1.05mm, allowing for effective work in previously enlarged canals. The #32 handle offers a grip adapted to the precision movements required during condensation. The curvature and angle of the working part are optimized for posterior (postér) areas, facilitating the passage of instruments in sectors where mouth opening is limited. Manufactured under the supervision of the manufacturer Hu-friedy in Chicago, this Class I device is a robust instrument designed to undergo the cleaning and sterilization cycles necessary in a dental office.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, contraindications are related to the intended use and safety warnings. The use of this instrument from the brand Hu-Friedy is strictly reserved for qualified healthcare professionals. It must not be used outside the clinical framework defined for endodontics. Although the source text does not list specific physiological contraindications such as allergies to unspecified metals, the practitioner must systematically refer to the instructions for use before any intervention. Failure to follow sterilization protocols or use on a dental structure not compatible with the 1.05mm dimensions of the instrument constitute technical contraindications to its use.
What are the maintenance and handling precautions?
Like any Class I instrument intended for dental surgery, this plugger requires rigorous maintenance. Before the first use and after each procedure, it must be cleaned, disinfected, and sterilized in accordance with the instructions from the manufacturer Hu-friedy. The practitioner must inspect the 1.05mm tip to ensure the absence of deformation or corrosion that could compromise the integrity of the endodontic treatment. During condensation, excessive pressure must be avoided to prevent any risk of root fracture. Handling must be carried out with care to preserve the calibration of the active part. It is imperative to read the instructions carefully to respect the maintenance cycles recommended by the brand Hu-Friedy.
Who is the manufacturer and what standards are respected?
This device is produced by the manufacturer Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. It is classified as a Class I medical device according to current regulations. This classification indicates that the instrument meets the basic safety and performance standards for manual surgical tools. Although specific CE marking is not mentioned in the source data, the product complies with manufacturing requirements for medical devices reserved for healthcare professionals. Traceability and manufacturing quality are ensured by the expertise of Hu-friedy, guaranteeing that this instrument from the brand Hu-Friedy can be safely integrated into the therapeutic arsenal of dental offices.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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