Root Elevator Miller - Helmut Zepf (17.100.10) - Delynov
The Élévateur à racines Miller - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.100.10.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Miller root elevator?
The Miller root elevator, bearing reference 17.100.10, is a specialized manual instrument designed by Helmut Zepf Medizintechnik GmbH. This dental miller elevator is manufactured from high-quality medical stainless steel to meet the requirements of oral surgery. Its structure is specifically designed to offer optimal grip during extraction procedures. As a Class I device, it complies with the rigorous manufacturing standards imposed on non-invasive or temporary-use invasive surgical instruments. This tool is delivered non-sterile and requires a complete cleaning and sterilization protocol before its first use in a dental office or hospital environment.
What are the clinical indications for this instrument?
This instrument is primarily indicated as a manual dental instrument for exodontia procedures. It is used by dental surgeons and implantologists for the luxation of dental roots, thereby facilitating their extraction from the alveolar socket. The dental miller elevator allows for intervention on difficult-to-access roots or root fragments remaining after a crown fracture. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery techniques. It plays a crucial role in preparing the alveolar site, particularly in implant placement protocols where the integrity of the bone walls must be preserved during extraction.
What are the technical characteristics of elevator 17.100.10?
The Miller root elevator from Helmut Zepf is distinguished by its robust medical stainless steel design. This material ensures the necessary resistance to the torsional forces applied during luxation. Technical reference 17.100.10 corresponds to a specific design in the Helmut Zepf Medizintechnik GmbH range, guaranteeing compatibility with standard thermal and chemical reprocessing protocols. The instrument is designed to be durable, although the manufacturer specifies that no maximum limit for processing cycles can be defined a priori. It is the practitioner's responsibility to visually check the condition of the instrument, specifically the absence of cracks, breaks, or defects on the active parts before each intervention.
What are the contraindications for the use of this elevator?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the surgical act, the procedure must be immediately interrupted and necessary medical measures must be taken. Apart from this material-related contraindication, the use of the instrument is contraindicated in case of visible damage to the tool, such as cracks or blunt cutting edges, as this could compromise patient safety and the effectiveness of the surgical maneuver.
What are the maintenance and sterilization precautions?
Like all Helmut Zepf Medizintechnik GmbH products, this dental miller elevator is delivered non-sterile. It is imperative to perform complete cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. The reprocessing process must follow the manufacturer's safety instructions to ensure the elimination of any contaminants. Before each use, the practitioner must carefully inspect the instrument for any signs of wear or degradation. The use of damaged or worn products is strictly prohibited. The longevity of the instrument depends directly on compliance with these maintenance protocols and proper handling during cleaning phases.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). The manufacturer ensures the conformity of its instruments with the regulatory requirements applicable to manual medical devices. The traceability and quality of the medical stainless steel used emphasize the Helmut Zepf brand's commitment to clinical safety. As a Class I instrument, it meets the essential safety and performance standards for its intended use in dental surgery, thus guaranteeing a reliable tool for oral healthcare professionals.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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