Elevating Seldin Number 34 with Handle Number 510 - Hu-Friedy - Delynov
The Elévateur Seldin #34 manche #510 - 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 Seldin #34 elevator handle #510?
The Seldin #34 elevator mounted on the #510 handle is a high-quality surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device, belonging to the oral surgery instrument category, is specifically designed for extraction procedures. Its structure is optimized to provide a grip adapted to the requirements of dental surgeons during luxation maneuvers. As a Class I instrument, it meets the rigorous manufacturing standards of the American manufacturer Hu-Friedy, recognized for its expertise in designing precision tools for the oral sphere.
What are the clinical indications for this seldin dental lever?
This seldin dental lever is primarily indicated for the luxation of teeth and roots prior to the use of forceps. In oral and implant surgery, it allows for the breaking of periodontal ligament fibers and the widening of the socket to facilitate extraction. Its use is particularly relevant during simple or complex avulsions where prior mobilization of the dental element is necessary. The instrument is exclusively reserved for use by qualified healthcare professionals, ensuring application in accordance with clinical protocols in force in dental offices and hospitals.
What are the technical characteristics of the instrument?
The Seldin #34 elevator is distinguished by the specific configuration of its working part associated with the #510 handle from the Hu-Friedy range. This combination is designed to effectively transmit leverage forces during root mobilization. Although the exact material composition is not specified in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC ensures a high industrial quality standard. The instrument is classified as a Class I medical device, which frames its marketing process and its use within the context of standard surgical care.
What are the contraindications for the use of this elevator?
According to the information provided by the manufacturer Hu-Friedy, specific indications and contraindications must be consulted in the instructions for use attached to the product. Generally, the use of this instrument is contraindicated for any person who does not have the qualification of a healthcare professional. It is imperative to read the instructions carefully before any intervention. Contraindications may include clinical situations where the application of leverage force could compromise critical adjacent anatomical structures or in cases of specific allergies to the metallic components of the surgical instrumentation.
What are the maintenance and durability precautions?
As a non-absorbable and reusable surgical steel instrument, the Seldin #34 elevator requires a strict sterilization protocol between each patient. Professionals must comply with the warnings from the manufacturer Hu-Friedy located in Chicago, USA, to ensure the tool's longevity. It is essential to check the integrity of the working part and the #510 handle before each use. Improper maintenance could alter the mechanical properties of the seldin dental lever, thereby compromising safety during extraction maneuvers. Compliance with cleaning and disinfection cycles is paramount to maintaining the conformity of this Class I device.
Who is the manufacturer and what standards are respected?
The device is manufactured by Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, Il 60618, USA. This product is classified as a Class I medical device. The manufacturer Hu-Friedy is a globally recognized entity in the dental sector for compliance with high-precision manufacturing standards. Although specific CE marking is not mentioned in the source data, the Class I classification indicates that the instrument meets the basic regulatory requirements for non-invasive or temporary-use invasive medical devices. Practitioners must systematically refer to the official technical documentation for any normative details.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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