MODIFIED ROOT ELEVATOR ACCORDING TO DENTIST BECK, 3.5mm - Helmut Zepf (17.201.01) - Delynov

What is the root elevator modified according to dentist Beck, 3,5mm?

The root elevator modified according to dentist Beck is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This device, referenced under code 17.201.01, consists of an ergonomic handle and a 3,5mm active part. Its structure is specifically designed to meet the requirements of dental surgeons during root luxation phases. The design of this dental beck elevator is based on a modification of classic models to optimize access and leverage during exodontia procedures. As an instrument in the Helmut Zepf range, it benefits from the expertise of a recognized manufacturer in the field of high-quality surgical instrumentation.

What are the clinical indications for this instrument?

This instrument is primarily indicated in oral surgery and implantology for the extraction of roots or teeth with decayed crowns. The beck root elevator allows for tooth mobilization by exerting controlled leverage and rotation forces. It is particularly useful for separating the root from its bony socket by severing the periodontal ligament fibers. Practitioners use this modified root elevator to prepare the site before immediate implant placement or to extract fractured root fragments. Its use is common in alveoloplasty procedures and during pre-implant surgeries requiring rigorous management of the surrounding hard tissues.

What are the technical characteristics of the 17.201.01 elevator?

The Helmut Zepf elevator (reference 17.201.01) features a 3,5mm active part, a standard dimension to adapt to the majority of root anatomies encountered in daily practice. The modification made according to the predictions of dentist Beck concerns the angulation and curvature of the tip, allowing for optimal transmission of manual force without excessive strain on the practitioner's wrist. The handle is designed to provide a stable grip, even in wet environments, ensuring precise tactile control when searching for the fulcrum. The robustness of the assembly between the shaft and the handle ensures increased longevity of the instrument during repeated sterilization cycles in the dental office.

What are the contraindications for the use of this elevator?

Contraindications for the use of the dental beck elevator are mainly related to the patient's clinical conditions and the surgical technique employed. It should not be used if the surrounding alveolar bone is too fragile or presents active tumor pathologies likely to spread. Furthermore, the use of excessive leverage forces is contraindicated on adjacent teeth carrying fragile fixed prostheses or unstable restorations, at the risk of causing collateral damage. As with any metal instrument, a contraindication may exist in case of known patient hypersensitivity to the alloy components, although this is rare with the standard surgical steels used by Helmut Zepf.

What are the maintenance and durability precautions?

As a non-resorbable and reusable instrument, this beck root elevator requires a strict protocol of cleaning, disinfection, and sterilization after each use. It is recommended to scrupulously follow the instructions from the manufacturer Helmut Zepf Medizintechnik GmbH regarding compatible decontamination products to avoid any corrosion or surface degradation. Before each intervention, the practitioner must inspect the condition of the 3,5mm active part to ensure the absence of micro-cracks or deformations. Regular lubrication of joints, if applicable, and storage in a dry environment help maintain the mechanical properties of the surgical steel over the long term.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a German company specializing in high-tech dental and surgical instrumentation. Although specific details of the CE marking or regulatory class are not explicitly stated in the short documentation, Helmut Zepf products are generally manufactured according to the rigorous quality standards of the European medical industry. Practitioners can refer to the instructions for use attached to the product or contact Delynov to obtain certificates of conformity and details regarding current ISO standards. Compliance with these standards ensures that the 17.201.01 elevator meets the safety and performance requirements for use in a clinical setting.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.