Root Elevator 2 mm - Helmut Zepf (17.001.10) - Delynov

What is the Helmut Zepf 2 mm root elevator?

The 2 mm root elevator, referenced under code 17.001.10 by the manufacturer Helmut Zepf Medizintechnik GmbH, is a manual instrument designed for dental and oral surgery. Manufactured from medical stainless steel, this tool consists of a 2 mm wide working part adapted to narrow alveolar spaces. Its rigid structure allows for the application of forces necessary for the mobilization of root fragments. This device belongs to Class I of medical devices, guaranteeing its compliance with basic regulatory requirements for non-invasive or short-term invasive instrumentation.

What are the clinical indications?

This instrument is specifically indicated for tooth extraction procedures, particularly during the management of fractured or residual roots. In oral and implant surgery, it is used to luxate the root by inserting between the alveolar bone and the root wall. Its use facilitates avulsion by minimizing stress on the surrounding tissues. It is used by healthcare professionals during alveoloplasties or site preparations before implant placement, where the complete and clean extraction of all dental debris is imperative for subsequent bone healing.

What are the technical characteristics of this instrument?

The Helmut Zepf elevator (reference 17.001.10) features a 2 mm active tip, sized for precise insertion into the periodontal ligament. Designed in medical stainless steel, it offers the mechanical resistance essential to support leverage during luxation. The product is delivered non-sterile, which requires a strict processing protocol before its first use. Its design allows it to withstand repeated cycles of cleaning, disinfection, and sterilization, although no maximum cycle limit is defined by the manufacturer due to the durable nature of the materials used.

What are the contraindications for use?

The main medical contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is manufactured from medical stainless steel, any contact with a patient presenting such an allergy may trigger a hypersensitivity reaction. If an adverse reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any manipulation with this metallic instrument.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must be imperatively cleaned, disinfected, and sterilized before their first use as well as after each subsequent use. Before each intervention, the practitioner must perform a meticulous visual inspection to detect any possible damage or signs of wear, such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn instrument is strictly prohibited. Furthermore, compatibility with other products used during the procedure must be verified beforehand to ensure the safety of the surgical treatment.

Who is the manufacturer and what standards are respected?

The official manufacturer of this elevator is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer specifies that the use of this instrument is strictly reserved for qualified healthcare professionals. As a medical stainless steel device, it meets the safety and performance requirements for manual instrumentation. Compliance with reprocessing protocols (cleaning and sterilization) is essential to maintain product conformity throughout its useful life.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.