Root Apex Elevator - Helmut Zepf (17.301.00) - Delynov

What is the Helmut Zepf apical root elevator?

The Helmut Zepf apical root elevator, bearing reference 17.301.00, is a manual instrument specifically designed for tooth extraction procedures. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device is intended for the manipulation of root structures. Its structure is designed to meet the requirements of oral surgery, offering resistance adapted to mechanical constraints during luxation. As a Class I instrument, it meets German manufacturing quality standards, ensuring reliability for daily procedures in dental practices or hospital environments.

What are the clinical indications for this instrument?

This instrument is indicated for the extraction of roots or root fragments, particularly in situations where access is limited. In oral and implant surgery, it can be used as an apical syndesmotome to separate the epithelial attachment and sever the ligament fibers surrounding the root. Its use is recommended during the avulsion of fractured teeth or deeply anchored residual roots. It allows for effective mobilization of the dental element before using extraction forceps, thus facilitating the surgical protocol while preserving the integrity of the surrounding alveolar walls.

What are the technical characteristics of reference 17.301.00?

The Helmut Zepf 17.301.00 elevator is characterized by its high-quality medical stainless steel manufacture, selected for its biocompatibility and corrosion resistance. It is a non-sterile manual instrument that requires a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. The technical design of the working part is optimized for insertion into the periodontal space. Due to its metallic nature, a prior check for the absence of hypersensitivity to steel components in the patient is necessary before any clinical intervention.

What are the contraindications for the use of this elevator?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known intolerance or hypersensitivity of the patient to metals, particularly medical stainless steel. If an allergic reaction or hypersensitivity reaction occurs during the procedure, the process must be immediately interrupted and appropriate medical measures taken. Furthermore, the use of the instrument is strictly prohibited if visible damage is detected, such as cracks, breaks, or defects on the cutting edges, to ensure the safety of the patient and the practitioner.

What are the maintenance and reprocessing precautions?

Helmut Zepf products are delivered non-sterile and must undergo complete reprocessing before use. This includes cleaning, disinfection, and sterilization in accordance with current protocols. Before each use, the practitioner must meticulously inspect the instrument to identify any signs of wear or damage. Due to the design and materials used, there is no defined maximum limit for treatment cycles, but the use of damaged products is formally prohibited. Compatibility with other products used during the sterilization chain must also be verified beforehand.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. This medical device is classified as Class I according to current regulations. The manufacturer imposes strict safety instructions, specifying that the use of this instrument is exclusively reserved for qualified healthcare professionals. Compliance with cleaning and sterilization protocols is essential to maintain the instrument's conformity with safety requirements. Helmut Zepf's commitment to manufacturing quality ensures dental surgeons a tool that meets the necessities of modern clinical practice.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.