Elevator number 81 with narrow upper handle - Hu-Friedy - Delynov
The Elévateur #81 manche #510 sup. étroit - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the #81 narrow #510 handle Hu-Friedy elevator?
The #81 elevator with #510 handle is a manual surgical instrument developed by the manufacturer Hu-Friedy Mfg. Co., LLC. This device is distinguished by a narrow upper working part, mounted on an ergonomic #510 type handle. It is designed to be inserted into the periodontal space to facilitate the separation of the root from its ligamentous attachments. As a precision instrument, it meets the requirements of practitioners performing complex extractions where access is limited by the thinness of the root structures. Its robust structure guarantees efficient transmission of force during luxation, while respecting the integrity of the surrounding alveolar bone.
What are the clinical indications for this instrument?
The use of this upper root elevator is primarily indicated during simple or complex dental extractions involving the maxillary arch. In oral and implant surgery, it is used to mobilize upper roots before their final removal. Its narrow configuration is particularly suitable for treating fractured roots or teeth with reduced interproximal space. The instrument allows for the application of controlled leverage to break the periodontal ligament fibers. This clinical maneuver is essential for reducing tissue trauma and preserving the alveolar walls, a critical step for the success of future implant placement or bone regeneration procedures.
What are the technical characteristics of the handle and the active part?
The Hu-Friedy narrow dental elevator combines a #510 handle and an active tip referenced as #81. The #510 handle is designed to provide a stable grip, allowing the surgeon to exert precise axial and rotational pressure without slipping. The narrow working part is specifically oriented to reach difficult access areas in the upper region. Hu-Friedy's manufacturing quality ensures high resistance to torsion, preventing tip deformation during the luxation of strongly anchored roots. This device is classified as a Class I instrument according to medical device regulations, guaranteeing its compliance with safety standards for non-invasive or reusable surgical instruments.
What are the contraindications for the use of this elevator?
In accordance with information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than inappropriate use by untrained personnel or in clinical situations where leverage extraction could damage adjacent critical anatomical structures, such as the maxillary sinus in cases of immediate root proximity. The practitioner must assess bone density and root condition via imaging before any intervention. It is imperative to follow sterilization and maintenance protocols to avoid any risk of cross-contamination or mechanical failure of the instrument.
What are the maintenance and durability precautions?
Although this instrument is not a resorbable device, its durability depends on strict adherence to the cleaning and sterilization cycles recommended by Hu-Friedy. As a Class I device, it must be inspected before each use for any signs of wear, corrosion, or cracks, particularly at the junction between the shaft and the #510 handle. The accumulation of organic residues can compromise sterilization efficiency and the longevity of the steel. It is recommended to use neutral pH cleaning solutions and avoid abrasive agents that could alter the surface finish of the upper elevator, thus ensuring consistent performance during repeated surgical procedures.
Who is the manufacturer and what standards are met?
The elevator is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized for the quality of its surgical instrumentation. The product is listed under regulatory Class I, which implies compliance with safety and performance requirements for medical devices in this category. Hu-Friedy applies rigorous manufacturing standards to ensure the reliability of its instruments. Healthcare professionals must imperatively read the instructions for use and warnings provided by the manufacturer carefully before any clinical implementation to ensure patient safety and treatment efficacy.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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