Root Elevator - Figure - LLM - Helmut Zepf (17.395.02)

What is the Lindo-Levien LLM root elevator?

The Lindo-Levien root elevator, referenced under code 17.395.02 by Helmut Zepf, is a precision manual instrument used in dental surgery. Manufactured from medical stainless steel, this tool is specifically designed for root manipulation. Its robust structure allows for the application of forces necessary for luxation without compromising the integrity of the instrument. As a device from the Helmut Zepf brand, it benefits from the expertise of Helmut Zepf Medizintechnik GmbH in the design of high-performance surgical tooling. This LLM model is delivered non-sterile and requires a rigorous preparation protocol before any clinical intervention.

What are the clinical indications for this instrument?

This elevateur racines llm is indicated for complex dental extraction procedures where the mobilization of a root or root fragment is necessary. Its primary use concerns oral surgery and implantology, particularly during alveoloplasty or the extraction of fractured teeth. The instrument allows the practitioner to access the alveolar space to separate ligament attachments. In accordance with the indications from the manufacturer Helmut Zepf, it is intended exclusively for professional use by qualified healthcare practitioners. Its application must take place in a controlled surgical environment, after verifying compatibility with other devices used during the procedure.

What are the technical characteristics of reference 17.395.02?

The Lindo-Levien elevator (reference 17.395.02) is distinguished by its ergonomic design adapted to the requirements of manual surgery. Although specific dimensions are not detailed, its classification as a Class I instrument highlights its compliance with regulatory standards for non-invasive or short-term invasive devices. The material used is a medical stainless steel selected for its mechanical resistance during lever maneuvers. Helmut Zepf Medizintechnik GmbH delivers this product non-sterile, implying that each instrument must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient to ensure clinical safety.

What are the contraindications for the use of this elevator?

The main medical contraindication identified for the use of this instrument is known hypersensitivity or intolerance of the patient to metals, specifically to medical stainless steel. An allergic reaction can be triggered during contact between the instrument and tissues. The manufacturer specifies that if such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before use. Additionally, the use of an instrument showing visible damage, such as cracks or defects on the cutting edges, is strictly prohibited.

What are the maintenance and reprocessing precautions?

Reprocessing of the Helmut Zepf elevator must follow a strict protocol: cleaning, disinfection, and sterilization. Before each use, the practitioner must inspect the instrument to detect any signs of wear, breakage, or corrosion. Due to the quality of the materials used by Helmut Zepf Medizintechnik GmbH, there is no defined maximum limit of treatment cycles, as long as the physical integrity of the tool is preserved. However, any damaged or worn product must be immediately removed from service. Compatibility with cleaning agents and sterilization methods must be verified beforehand to maintain the mechanical properties of the medical stainless steel.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. The product is classified as a Class I medical device, meeting the regulatory requirements of its category for manual instruments. Although specific CE marking is not mentioned in the source data, compliance with the rigorous manufacturing protocols of Helmut Zepf ensures consistent quality. As a Class I device, it is subject to the safety and performance controls applicable to reusable surgical instruments, thus guaranteeing its reliability for daily oral surgery interventions.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.