Elevator X-Luxatool 2 - Helmut Zepf (17.007.02TI) - Delynov

What is the Helmut Zepf X-Luxatool 2 elevator?

The X-Luxatool 2 elevator, bearing reference 17.007.02TI, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from medical stainless steel, a standard material for surgical instrumentation ensuring the robustness necessary for extraction procedures. As a Class I device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use. Its structure is specifically designed to offer a grip adapted to the needs of dental surgeons during alveolar luxation maneuvers.

What are the clinical indications for this instrument?

The intended use of this Helmut Zepf instrument is strictly defined for dental surgery. It is indicated for lifting teeth or residual dental roots during an extraction procedure. Its primary clinical role is to facilitate the separation of the tooth from its ligamentous attachment and the bony socket. It is particularly used in cases of fractured roots or difficult-to-access root remains, where a controlled leverage force is necessary to mobilize the dental element before its final removal.

What are the technical characteristics of the 17.007.02TI elevator?

The X-Luxatool 2 elevator is distinguished by its high-quality medical stainless steel design, selected by Helmut Zepf for its mechanical resistance. This device is delivered non-sterile and requires a complete reprocessing protocol before each use. Although the manufacturer does not define a maximum limit for treatment cycles due to the nature of the materials used, the instrument must undergo a rigorous visual inspection. The practitioner must check for the absence of cracks, breaks, or defects on the cutting edges before any intervention.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer concerns the patient's known hypersensitivity to metals. Contact with the medical stainless steel of the instrument may trigger an intolerance reaction in certain individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. It is therefore crucial to assess the patient's allergic history before using this manual instrument during an extraction.

What are the maintenance and sterilization precautions?

As a non-sterile reusable instrument, all Helmut Zepf devices must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The cleaning process must be complete to ensure the elimination of all biological residues. It is imperative to never use products that are damaged or show visible wear, as this could compromise patient safety or the effectiveness of the surgical procedure. Compatibility with other products used during the sterilization chain must also be verified beforehand.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects the manufacturing standards for Class I medical devices. The product is exclusively reserved for use by qualified healthcare professionals. The traceability and quality of the stainless steel used meet the requirements of the dental sector for manual instruments. Each step, from design to distribution by Delynov, follows strict protocols to ensure compliance with medical device regulations.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.