Glick #1 gutta-percha plugger #6 handle 1.10mm
The Fouloir à gutta Glick #1 manche #6 1,10mm 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 Glick #1 gutta-percha plugger handle #6 1.10mm?
The Glick #1 gutta-percha plugger from the brand Hu-Friedy is a specialized manual instrument used in endodontics. This device consists of a #6 size handle offering a grip adapted to the requirements of dental surgery. Its double-ended design allows for alternating between condensation and cutting phases without changing instruments. The 1.10mm active part is calibrated to intervene effectively within canal structures. Manufactured under the supervision of the manufacturer Hu-friedy, this instrument meets the quality standards required for Class I medical devices, thus guaranteeing reliability during daily clinical procedures.
What are the clinical indications?
This device from the brand Hu-Friedy is indicated for root canal obturation procedures in endodontics. It is specifically used by healthcare professionals for vertical compaction of gutta-percha, thereby ensuring optimal apical sealing. In addition to its plugger function, the Glick #1 allows for clean sectioning of excess gutta-percha cones after thermal softening. Its use is strictly reserved for dental surgeons and specialists performing complex or routine endodontic care, requiring precise control of the pressure exerted on the filling materials inside the canal system.
What are the technical characteristics?
The Glick #1 plugger is distinguished by its 1.10mm diameter at the active tip, a standardized dimension for endodontic treatments. The instrument features a #6 handle, designed to offer optimal balance during intra-oral manipulations. The functional double end allows for immediate versatility in the operating field. As a product of the brand Hu-Friedy, it benefits from the manufacturing expertise of Hu-friedy, located in the USA. This device is classified as Class I according to current regulations, which confirms its status as a non-invasive instrument reusable after sterilization, in accordance with hospital and dental office hygiene protocols.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, there are no specific medical contraindications listed for this instrument, other than those related to standard endodontic protocols. However, the use of this product from the brand Hu-Friedy is strictly reserved for qualified healthcare professionals. Use by untrained personnel could lead to clinical complications. It is imperative to read the instructions carefully before use to ensure compliance with safety guidelines. The practitioner must also check the integrity of the instrument before each intervention to prevent any risk of instrumental fracture or mucosal injury.
What are the maintenance precautions for this non-resorbable device?
As this is a manual metal instrument and not a suture, the concept of resorption does not apply. However, to maintain the performance of the Glick #1 plugger from the brand Hu-Friedy, strict cleaning and sterilization precautions must be followed. After each surgical use, the instrument must be decontaminated, cleaned, and sterilized according to the instructions of the manufacturer Hu-friedy. It is advisable to use cleaning solutions that do not alter the physical properties of the instrument. Regular inspection of the 1.10mm tip is necessary to detect any signs of wear or deformation that could compromise the precision of the gutta-percha compaction.
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 USA. This product is marketed under the brand Hu-Friedy and complies with the regulatory requirements for Class I medical devices. 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, compliance with the manufacturer Hu-friedy's directives ensures that the instrument is suitable for professional use in a clinical environment. Compliance with the manufacturer's warnings is essential to ensure patient and practitioner safety.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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