Elevator X - LUXA - TOOL - 1 - Helmut Zepf (17.007.01) - Delynov

What is the X - LUXA - TOOL - 1 - Helmut Zepf (17.007.01) elevator?

The X - LUXA - TOOL - 1 elevator, referenced under code 17.007.01 at Delynov, is a high-precision manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. This medical device is manufactured from medical-grade stainless steel, ensuring the robustness required for oral surgery interventions. Its structure is specifically designed to facilitate handling during extraction procedures. As a reusable instrument, its design allows it to undergo repeated processing cycles without a maximum limit defined by the manufacturer, subject to rigorous inspection before each use. This instrument belongs to the category of durable consumables for dental practices and clinics specializing in oral surgery.

What are the clinical indications for this Helmut Zepf instrument?

The intended use of this Helmut Zepf instrument is strictly defined for the dental field. It is primarily indicated as a manual instrument for lifting teeth or extracting residual dental roots during surgical extraction procedures. Its ergonomic design allows the practitioner to exert controlled force to luxate the tooth or root fragment from the socket. This device is exclusively reserved for qualified healthcare professionals, such as dental surgeons, stomatologists, and implantologists, who have mastered minimally invasive extraction techniques. The use of this elevator facilitates the preservation of surrounding bone structures by allowing effective separation of periodontal tissues before the final removal of the dental element.

What are the technical characteristics of the 17.007.01 elevator?

The X - LUXA - TOOL - 1 elevator is distinguished by its medical stainless steel construction, a material chosen for its mechanical resistance and its ability to withstand sterilization processes. This model, bearing technical reference 17.007.01, is delivered non-sterile by Helmut Zepf Medizintechnik GmbH. Before any initial use, the instrument must undergo a complete cleaning, disinfection, and sterilization protocol. The manufacturer emphasizes that the instrument's lifespan depends on its design and the materials used; there is no predefined limit on processing cycles, but the user must imperatively check for the absence of visible damage such as cracks, breaks, or defects on the cutting edges before each procedure.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns the patient's known hypersensitivity to metals. Contact with medical stainless steel can trigger an allergic reaction or intolerance in certain individuals. If a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken accordingly. Furthermore, the use of the instrument is strictly contraindicated if it shows signs of wear or visible damage, such as cracks or blunt cutting edges, as this could compromise patient safety and the effectiveness of the surgical act. It is also imperative to verify compatibility with other products used simultaneously.

What are the maintenance and safety precautions?

To ensure clinical safety and instrument longevity, all Helmut Zepf devices must be cleaned, disinfected, and sterilized before the first use, as well as before each subsequent use. Prior cleaning is a critical step that must be performed carefully to remove all biological residues. It is essential to visually inspect the instrument for any signs of wear, corrosion, or deformation. The use of damaged products is strictly prohibited. Although reprocessing is not limited to a fixed number of cycles, the vigilance of the healthcare professional is required to determine if the instrument retains its functional properties. Strict compliance with the manufacturer's instructions for use and safety is essential to prevent any risk of cross-contamination or intraoperative incidents.

Who is the manufacturer and what standards are respected?

The elevator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is regulatory classified as Class I according to medical device directives. As a Class I instrument, it meets the safety and performance requirements imposed for this category of manual surgical tools. The products are delivered non-sterile and must be processed in accordance with standard hospital sterilization protocols. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Traceability and technical compliance are ensured by reference 17.007.01, guaranteeing the origin and German manufacturing quality of the Helmut Zepf brand within the Delynov catalog.

State of the art

Surgical medical consumables play a decisive role in operative safety and tissue regeneration quality.