Root Apex Elevator - Helmut Zepf (17.304.00) - Delynov

What is the Helmut Zepf Apical root elevator?

The Apical root elevator - Helmut Zepf (reference 17.304.00) is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is specifically developed for alveolar surgery procedures requiring fine manipulation of radicular structures. It belongs to the category of extraction instruments and is distinguished by its structural robustness adapted to the mechanical constraints of luxation. This device is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use in a dental practice or operating theater.

What are the clinical indications for this instrument?

This dental apical elevator is indicated for the extraction of roots and apexes, particularly in situations where access is restricted or when the root is fractured below the crestal level. In oral and implant surgery, it is used to break the periodontal ligament fibers to mobilize the tooth before its final removal. The apical extraction instrument is used by healthcare professionals to facilitate avulsion while best preserving the integrity of the alveolar walls, a crucial step for future implant placement or bone regeneration procedures.

What are the technical characteristics of the 17.304.00 elevator?

The Apical root elevator referenced 17.304.00 by Helmut Zepf is manufactured from medical stainless steel selected for its corrosion resistance and its ability to maintain functional active edges. Although specific dimensions are not detailed, its design meets the requirements of Class I medical devices. The geometry of its working part is optimized to fit into the desmodontal space. As a Helmut Zepf Medizintechnik GmbH product, it benefits from rigorous German engineering guaranteeing compatibility with standardized reprocessing protocols in an autoclave, with no defined maximum limit of treatment cycles subject to proper maintenance.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance of the patient to metals, particularly medical stainless steel. A hypersensitivity reaction can be triggered during contact between the instrument and the tissues. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary clinical measures must be taken. Furthermore, the use of the instrument is strictly prohibited if it shows visible damage such as cracks, breaks, or defects on the cutting edges, in order to guarantee patient safety and the efficiency of the surgical gesture.

What are the maintenance and reprocessing precautions?

Like any reusable Class I instrument, the Apical root elevator must undergo a strict reprocessing protocol. Before each use, the practitioner must check for the absence of visible wear or deformations. The process imperatively includes thorough cleaning, disinfection, and sterilization, as Helmut Zepf products are delivered non-sterile. Due to the quality of the materials used, there is no predefined maximum limit of use cycles, but the longevity of the instrument directly depends on compliance with the manufacturer's cleaning and safety instructions. The use of damaged products is dangerous and formally discouraged.

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 (Class Ir according to certain reprocessing nomenclatures). It meets the regulatory requirements for manual dental instruments. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals. Compliance with manufacturing standards guarantees that the medical stainless steel used is suitable for prolonged tissue contact during surgical acts, subject to compliance with current sterilization protocols.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.