Root Elevator - Helmut Zepf (17.396.01) by Lindo-Levien - Delynov

What is the Helmut Zepf Lindo-Levien root elevator?

The Lindo-Levien (reference 17.396.01) is a manual instrument designed by Helmut Zepf Medizintechnik GmbH for dental surgery. Manufactured from medical stainless steel, this robust tool is specifically structured to meet the requirements of root extractions. As a Class I device, it is intended for strict professional use in dental practices or hospital environments. Its morphology is adapted to insert into the periodontal space to break the supporting fibers of the tooth, thus allowing effective mobilization of the roots before removal.

What are the clinical indications for this instrument?

The use of this surgical root elevator is indicated during simple or complex tooth extraction procedures. It is primarily used for the luxation of roots remaining in place after a crown fracture or during the extraction of multi-rooted teeth that have been previously separated. In oral and implant surgery, it allows for the preparation of the alveolar site by clearing root fragments without excessively damaging the surrounding bone walls. Its use is reserved for qualified healthcare professionals mastering exodontia techniques.

What are the technical characteristics of the Lindo-Levien 17.396.01?

This Helmut Zepf instrument is characterized by its manufacture from high-quality medical stainless steel, guaranteeing the necessary resistance to the leverage forces applied during surgery. Referenced under code 17.396.01, it features an ergonomic working part designed for precise insertion. In accordance with the manufacturer's directives, the device is delivered non-sterile and must imperatively undergo a full cycle of cleaning, disinfection, and sterilization before its first use and between each patient to ensure aseptic safety.

What are the contraindications for the use of this elevator?

The main medical contraindication documented by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance of the patient to metals, specifically medical stainless steel. If a hypersensitivity reaction is triggered upon contact with the instrument during the intervention, the procedure must be immediately stopped and necessary clinical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any surgical handling with this Class I device.

What are the maintenance and reprocessing precautions?

Like any reusable Helmut Zepf instrument, this elevator requires a rigorous reprocessing protocol. Before each use, the practitioner must visually inspect the instrument to detect potential damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited. Although there is no defined maximum limit of sterilization cycles due to its robust design, compatibility with other cleaning products and verification of functional wear are essential to maintain the tool's integrity.

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 according to current regulations. The manufacturer requires that all instruments be cleaned, disinfected, and sterilized before any use, as they are delivered non-sterile. Compliance with the safety and use instructions provided by Helmut Zepf is imperative to guarantee the performance of the instrument and patient safety during dental surgery procedures.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.