Surgical root elevator with finger rest, width 5mm - Helmut Zepf (17.001.13) - Delynov

What is the Helmut Zepf surgical root elevator (17.001.13)?

The Helmut Zepf root elevator, reference 17.001.13, is a specialized manual instrument intended for oral and implant surgery. This device is distinguished by a working part with a width of 5 mm and a structure integrating a specific finger rest. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is designed to offer maximum stability during luxation maneuvers. Its configuration allows for the efficient transmission of the force necessary to separate the root from its alveolar environment. It is a robust tool, developed to meet the requirements of repeated sterilization and durability inherent to professional surgical environments.

What are the clinical indications for this instrument?

This elevator is primarily indicated for the extraction of dental roots or root debris during exodontia surgeries. Its 5 mm width makes it particularly useful for areas requiring a wider contact surface, thus facilitating the luxation of voluminous roots. In implant surgery, it can be used to prepare the alveolar site by clearing residual dental structures. The finger rest allows the practitioner to exert controlled pressure, limiting the risk of slipping when applying leverage between the alveolar bone and the root. Its use is recommended to facilitate the expansion of the socket before final extraction.

What are the technical characteristics of the 17.001.13 elevator?

The Helmut Zepf 5mm root elevator features precise technical characteristics focused on clinical performance. Reference 17.001.13 specifies an instrument equipped with a 5 mm wide blade, optimized to fit into the periodontal space. The major technical element lies in its ergonomic handle equipped with a finger rest, designed to improve grip and the transfer of axial and rotational force. The manufacturing quality of Helmut Zepf Medizintechnik GmbH guarantees a rigorous fit between the shaft and the working part. This instrument is designed to withstand the high mechanical stresses associated with luxation without deformation, while allowing for cleaning and decontamination in accordance with hospital protocols.

What are the contraindications for the use of this instrument?

Although specific manufacturer data does not list restrictive medical contraindications, the use of this elevator should be avoided in situations where the integrity of the adjacent alveolar bone must be absolutely preserved without any expansion, or in the presence of critical anatomical structures (nerves, sinuses) too close to the support area. As with any metallic surgical instrument, a contraindication may exist in case of known patient hypersensitivity to the alloy components, although this is rare with standard surgical steels. It is the surgeon's responsibility to evaluate bone density and root fragility to avoid any unwanted root fracture during the application of force.

What are the maintenance precautions for this non-resorbable instrument?

As a reusable steel surgical instrument, the Helmut Zepf elevator requires a strict sterilization protocol after each intervention. It is imperative to follow the manufacturer's recommendations regarding thermal cleaning and autoclave sterilization. Precautions include the use of non-corrosive cleaning solutions and complete drying of the instrument to prevent any pitting corrosion. The finger rest and junction areas must receive special attention during brushing to remove any organic residue. Regular visual inspection of the condition of the 5 mm blade is necessary to ensure the absence of dulling or micro-cracks, thus guaranteeing patient safety and the effectiveness of the surgical procedure.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of dental and surgical instrumentation based in Germany. The Helmut Zepf brand is synonymous with precision and quality in the medical sector. Although the specific regulatory class and CE marking are not detailed in the current technical sheet, this manufacturer's products are generally designed according to rigorous international quality standards. To obtain precise information on certificates of conformity, ISO standards respected, or the specific CE marking for reference 17.001.13, it is recommended to refer to the instructions for use provided by the manufacturer or to contact Delynov's technical service directly.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.