Root Elevator - Helmut Zepf (17.396.03) - Delynov
The Lindo-Levien Élévateur à Racines - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.396.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Lindo-Levien root elevator?
The Lindo-Levien root elevator, referenced under code 17.396.03, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this instrument is specifically structured to meet the requirements of oral surgery and tooth extraction. Its morphology is studied to allow optimal handling during root luxation. As a Class I device, it meets the quality standards required for temporary-use invasive instruments. This product is delivered non-sterile by the manufacturer and requires a complete cleaning and sterilization protocol before its first use in the office or operating room.
What are the clinical indications for this instrument?
This lindo levien root elevator is primarily indicated for simple or complex extraction procedures. Its clinical role consists of facilitating the separation of the root from its ligamentous attachment (periodontal ligament) and extracting it from the socket. It is particularly useful for mobilizing fractured roots or deep radicular fragments that cannot be grasped by standard surgical forceps. The use of this Helmut Zepf instrument is reserved exclusively for qualified healthcare professionals, such as dental surgeons and stomatologists, trained in exodontia and alveolar surgery techniques.
What are the technical characteristics of the 17.396.03 elevator?
The Helmut Zepf Lindo-Levien elevator is distinguished by its robust medical stainless steel design, guaranteeing the mechanical resistance necessary during the applied leverage forces. Technical reference 17.396.03 corresponds to a specific configuration of the working part, optimized for access to surgical sites. Although the design is ergonomic, the manufacturer specifies that each instrument must be visually inspected before use to detect potential damage such as cracks, breaks, or defects on the cutting edges. The durability of the instrument depends on strict compliance with reprocessing cycles, although no maximum limit of cycles is defined by the manufacturer due to the quality of the materials used.
What are the contraindications for the use of this elevator?
The main medical contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns the patient's known hypersensitivity or intolerance to metals, specifically medical stainless steel. An allergic reaction may occur during contact between the instrument and the patient's tissues. If such a hypersensitivity reaction is triggered during the intervention, the procedure must be immediately stopped and the necessary clinical measures must be taken. It is therefore crucial to check the patient's allergic history before any surgical manipulation with this Class I metallic instrument.
What are the maintenance and reprocessing precautions?
The Lindo-Levien root elevator is a non-sterile device that must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. The manufacturer emphasizes the importance of carefully cleaning the product to remove all biological residue before sterilization. It is also imperative to check compatibility with other cleaning or disinfection products used. Any instrument showing visible signs of wear, corrosion, or deformation must be immediately removed from service to ensure patient safety and the effectiveness of the surgical procedure. Reprocessing must follow standard protocols in force for manual dental instrumentation.
Who is the manufacturer and what standards are respected?
The Lindo-Levien elevator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures the compliance of its products with safety and performance requirements for manual surgical instruments. As a Class Ir instrument, it is designed to be reused after an appropriate sterilization process. Compliance with the instructions provided by Helmut Zepf guarantees use in accordance with professional dental surgery standards, thus ensuring the technical reliability essential during root extraction procedures.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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