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Surgical dental root elevator, modified according to Dr. Beck, width 2.8mm - Helmut Zepf (17.200.01) - Delynov

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The Élévateur chirurgical de racines dentaires, modifié d'après le Dr. Beck, largeur 2,8 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 17.200.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

71.99 € 71.99 EUR 71.99 € Tax Included

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Instrument

What is the Helmut Zepf surgical elevator modified according to Dr. Beck?

The Helmut Zepf surgical elevator (reference 17.200.01) is a specialized instrument designed for root extraction. This specific model, modified according to Dr. Beck's principles, features an optimized structure for dental luxation. Its working part has a width of 2.8 mm, making it an instrument of choice for procedures requiring a fine approach. Manufactured by Helmut Zepf Medizintechnik GmbH, this tool is intended for practitioners demanding precision instruments for oral and implant surgery. Its design allows for rigorous handling during avulsion phases.

What are the clinical indications for this instrument?

This fine root elevator is primarily indicated for the luxation of dental roots prior to extraction. In oral surgery, its use allows for the separation of the root from its alveolar attachment by inserting it into the periodontal space. The 2.8 mm width is particularly suitable for treating a thin root or for intervening in areas where interdental space is limited. It is used during simple or complex extractions, as well as in site preparation before implant placement, where preservation of the alveolar bone walls is crucial for future clinical success.

What are the technical characteristics of the 17.200.01 elevator?

The elevator referenced 17.200.01 by Helmut Zepf is distinguished by its active tip of 2.8 mm in width. This specific dimension allows for atraumatic insertion into the periodontal ligament. The modification inspired by Dr. Beck concerns the angulation and ergonomics of the active part, providing the surgeon with an effective lever to mobilize the root. The monoblock design ensures direct and controlled force transmission. This instrument is designed to withstand repeated mechanical stress during luxation maneuvers while maintaining the integrity of its working end.

What are the contraindications for the use of this elevator?

Contraindications for the use of this Helmut Zepf instrument are related to the general limits of oral surgery. It should not be used if the practitioner judges that bone density or root fragility risks leading to an uncontrolled fracture under the pressure of the elevator. Furthermore, the use of this instrument is prohibited in cases of known allergy to the metallic components of surgical instrumentation. It is the surgeon's responsibility to evaluate the clinical situation and ensure that the instrument is adapted to the morphology of the root to be extracted to avoid any damage to adjacent structures.

What are the maintenance and durability precautions?

As a reusable surgical instrument, the Helmut Zepf elevator must follow a strict sterilization protocol between each patient. It is recommended to clean the instrument immediately after use to prevent the drying of biological debris. Compliance with cleaning, disinfection, and autoclave sterilization cycles is imperative to maintain the mechanical properties of the steel and guarantee asepsis. A visual inspection of the 2.8 mm tip is advised before each procedure to check for the absence of deformations or dullness that could compromise the effectiveness of the root luxation.

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 surgical and dental instrumentation. Helmut Zepf applies rigorous manufacturing standards to guarantee the reliability of its products. Although detailed regulatory specifications such as the exact class or CE marking are not specified in this document, Helmut Zepf products generally comply with European requirements relating to medical devices. For any precise information on certifications or ISO standards applied to reference 17.200.01, it is advisable to refer to the technical instructions provided by the manufacturer.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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