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Dental root elevator no. 22, sample model - Helmut Zepf (17.622.00) - Delynov

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The Élévateur de racines dentaires numéro 22, modèle selon échantillon - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 17.622.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

64.19 € 64.19 EUR 64.19 € Tax Included

64.19 € Tax Included

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Instrument

What is the Helmut Zepf dental root elevator number 22?

The dental root elevator number 22, referenced under code 17.622.00, is a precision manual instrument designed by Helmut Zepf Medizintechnik GmbH. This model, developed according to a specific sample, is intended for the practice of exodontia in oral surgery. Its structure is optimized for the grip and force transmission necessary for root luxation. As a device in the Helmut Zepf range, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation, offering practitioners a reliable tool for daily interventions in the dental office.

What are the clinical indications for this instrument?

This root elevator n22 is primarily indicated for dental avulsion procedures, whether for single extractions or more invasive surgeries. Its clinical role consists of separating the root from its socket by acting on the periodontal ligament. It is particularly useful for the extraction of residual roots or fractured teeth where gripping with forceps is impossible. The use of this root elevator n22 allows for the preparation of the site before the use of forceps, thereby reducing the risk of alveolar bone fracture during the final phase of avulsion.

What are the technical characteristics of elevator 17.622.00?

The dental elevator n22 is distinguished by its specific technical configuration identified by reference 17.622.00 at Helmut Zepf. Although exact dimensions are not specified, this model follows a standardized ergonomic design to allow for stable support and precise control of the lever movement. The working part is dimensioned to adapt to the root anatomy, ensuring effective insertion into the sulcus. Manufacturing by Helmut Zepf Medizintechnik GmbH guarantees rigorous assembly meeting the requirements of dental surgeons and implantologists regarding mechanical resistance during luxation maneuvers.

What are the contraindications for the use of this elevator?

The use of root elevator 22 is contraindicated in situations where the integrity of adjacent anatomical structures, such as the maxillary sinus or the mandibular canal, could be compromised by excessive pressure. Like any metallic instrument, its use must be avoided in patients with a known hypersensitivity to the alloy components, although the exact material specifications are not detailed here. It is the practitioner's responsibility to evaluate bone density and root fragility before any application of force, in order to prevent iatrogenic fractures or root projections into soft spaces.

What are the maintenance and storage precautions?

As a reusable surgical instrument from the Helmut Zepf brand, this elevator must imperatively undergo a complete cycle of decontamination, cleaning, and sterilization between each patient. It is recommended to follow standard autoclave protocols in force in dental care facilities. Precautions include the use of non-corrosive cleaning solutions to preserve the surface condition of the steel. A visual inspection of the working tip is necessary before each intervention to ensure the absence of deformations or micro-cracks that could alter the safety of the surgical procedure.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, an internationally renowned German company in the production of high-quality surgical tools. Although the precise regulatory class and CE marking are not mentioned in the source data, Helmut Zepf products are generally designed according to strict industrial standards to meet the requirements of healthcare professionals. For any specific information regarding certificates of conformity or ISO standards applied to reference 17.622.00, it is advised to refer to the technical documentation provided by the manufacturer or to consult the instructions for use accompanying the device.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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