Elevator Bone Number 559/1 with Handle Number 510 Wide - Hu-Friedy - Delynov
The Elévateur Bein #559/1 manche #510 large - 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 Hu-Friedy Bein #559/1 elevator?
The Bein #559/1 elevator from the brand Hu-Friedy is an oral surgery instrument designed for the luxation of teeth. This model is distinguished by its handle #510 and its wide working part, specifically developed for interventions requiring effective mobilization of dental structures. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is part of the manual exodontia device category. Its robust structure allows the practitioner to exert the necessary pressure during the initial phases of extraction, thus ensuring optimal preparation of the alveolar site before the use of forceps.
What are the clinical indications for this wide bein elevator?
This wide bein elevator is mainly indicated in oral surgery and implantology for the luxation of roots and teeth before their complete extraction. Its use allows for the sectioning of periodontal ligament attachments through a rotation and elevation movement. It is particularly useful for simple or complex extractions where prior root mobilization is required. As a wide syndesmotome, it helps create the necessary space between the alveolar bone and the root, facilitating tooth removal while preserving the integrity of surrounding tissues for potential grafting procedures or immediate implant placement.
What are the technical characteristics of this instrument?
The Hu-Friedy Bein #559/1 elevator presents precise technical characteristics adapted to clinical requirements. It is equipped with the handle type #510, offering specific ergonomics for force transmission. Its wide tip is designed to insert effectively into the desmodontal space. This device belongs to Class I of medical devices, guaranteeing its compliance with basic regulatory requirements for non-invasive or reusable surgical instrumentation after sterilization. The manufacturing quality of Hu-Friedy Mfg. Co., LLC ensures mechanical resistance adapted to the torsion and leverage stresses encountered during dental luxations.
What are the contraindications for the use of this instrument?
According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications include use on anatomical structures not intended by the device's destination. Although the raw MDR text does not list specific medical contraindications related to systemic pathologies, the practitioner must evaluate the state of the alveolar bone and root fragility before application. Inappropriate use or excessive force could lead to unwanted bone or root fractures. The instructions for use should be systematically referred to before any surgical intervention.
What are the maintenance and handling precautions?
As a Class I instrument, this elevator must undergo a rigorous cleaning, disinfection, and sterilization protocol between each patient, in accordance with Hu-Friedy guidelines. Being a non-resorbable device intended for repeated use, it is imperative to check the integrity of the wide working part before each use. Any trace of corrosion or deformation must lead to the withdrawal of the instrument to guarantee patient safety. Healthcare professionals must handle this tool with precision to avoid any damage to adjacent soft tissues during luxation, respecting the asepsis principles in force in the dental office.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is classified as Class I according to current medical device regulations. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instrumentation. The product meets the safety and performance requirements defined for manual oral surgery instruments. Compliance with the maintenance and sterilization protocols described by the manufacturer is essential to maintain the device's conformity and ensure its longevity within the surgical technical tray.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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