Schluger #9S/10S Bone File #2 Handle - Hu-Friedy - Delynov
The Lime Schluger #9S/10S manche #2 - 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 Schluger #9S/10S file handle #2 - Hu-Friedy?
The Schluger #9S/10S file is a high-precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device consists of a double working end, mounted on a #2 type handle, offering a grip adapted to periodontology procedures. As a manual instrument, it is specifically designed for the treatment of hard tissues. Its structure allows for rigorous manipulation during bone rectification phases. This product is part of the instrumentation range from Hu-Friedy, a manufacturer recognized for its expertise in the dental and surgical field, guaranteeing a tool that meets the requirements of specialized practices.
What are the clinical indications?
The clinical indications for the schluger file primarily concern periodontal and implant surgery. It is used by healthcare professionals for the remodeling of alveolar bone, particularly in cases of osteoplasty aimed at correcting bone defects or harmonizing gingival contours. This instrument is also requested for fine ostectomy, allowing for the removal of small amounts of bone around teeth or implant sites. Its use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-Friedy located in Chicago. It often intervenes as a complement to other resection instruments to finalize the bone surface condition.
What are the technical characteristics?
The Schluger #9S/10S file is distinguished by its double-ended configuration, optimizing efficiency during the intervention without changing instruments. The #2 handle is designed to provide the balance necessary for bone scraping and smoothing gestures. Manufactured by Hu-Friedy, this file meets the quality standards of surgical instrumentation. It is classified as a Class I device, which corresponds to non-invasive or short-term invasive reusable surgical instruments according to current regulations. The manufacturing details from Hu-Friedy Mfg. Co., LLC ensure resistance adapted to the mechanical stresses encountered during the remodeling of calcified structures in the mouth.
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 surgical protocols. However, its use is strictly reserved for healthcare professionals trained in oral surgery techniques. Failure to comply with sterilization protocols or use on inappropriate tissues could constitute an indirect contraindication. It is imperative to read the instructions carefully before use to ensure the compatibility of the device with the patient's clinical condition and the planned procedure.
What are the precautions for use and maintenance?
As a Class I instrument, the Schluger file requires rigorous maintenance to guarantee its longevity and the safety of care. Although composition details are not specified, this type of Hu-Friedy instrument must be cleaned, disinfected, and sterilized before each use in accordance with the instructions in the manual. Practitioners must inspect the condition of the working parts of the schluger file to detect any wear or dullness that could compromise the effectiveness of the bone remodeling. The warnings from the manufacturer Hu-Friedy specify that this device is intended for professional use only, requiring expert handling to avoid any damage to adjacent structures.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, thus meeting the regulatory requirements for instruments in its category. CE marking is not specified in the source documentation, but the product is subject to the strict manufacturing standards of Hu-Friedy, a historical player in dental instrumentation. Compliance with the manufacturer's indications and warnings is essential to ensure safe use in a clinical setting. Professionals must systematically refer to the instructions for use provided by Hu-Friedy.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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