Beck modified dental root elevator, 3.5mm - Helmut Zepf (17.201.02) - Delynov
The Élévateur de racines dentaires modifié Beck, 3,5 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.201.02.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Beck modified dental root elevator 3.5 mm?
The Beck modified dental root elevator is a manual oral surgery instrument designed by Helmut Zepf Medizintechnik GmbH. This device consists of an ergonomic handle and a specific 3.5 mm active part. Its structure is optimized to insert into the periodontal space to facilitate root mobilization. As an instrument in the Helmut Zepf range, it benefits from the German manufacturer's expertise in precision tool design. Reference 17.201.02 corresponds to a Beck modified model, offering geometry adapted to the requirements of complex extractions where access is restricted.
What are the clinical indications for this instrument?
This 3.5 mm dental elevator is primarily indicated for the luxation of single or multi-rooted roots during exodontia procedures. It is used in oral surgery to detach the periodontal ligament and create sufficient space for the insertion of forceps beaks. The Beck elevator is particularly useful for the extraction of roots that are fractured or remain below the gingival level. Its use reduces bone resistance through controlled leverage, promoting a less invasive extraction of dental structures. It is also suitable for pre-implant surgeries requiring careful management of the socket.
What are the technical characteristics of the Beck elevator 17.201.02?
The Beck elevator referenced 17.201.02 is distinguished by a tip width of 3.5 mm. This intermediate dimension allows for versatile use on different types of teeth, both in the maxilla and the mandible. The Beck modified design involves a curvature and thinness of the working part designed to penetrate the socket effectively. Manufactured by Helmut Zepf, the instrument is designed to withstand mechanical stresses exerted during rotation and elevation movements. The surface finish and assembly quality ensure precise force transmission between the practitioner's hand and the target root.
What are the contraindications for the use of this elevator?
Contraindications for the use of the Beck modified root elevator are related to the general clinical conditions of oral surgery. It should not be used if the patient presents serious systemic contraindications to dental extraction, such as uncontrolled coagulation disorders or specific bone pathologies. Technically, its use is discouraged if the root morphology or surrounding bone density risks causing instrument fracture in case of excessive force. The practitioner must ensure the instrument is used only for its intended use and on anatomical structures compatible with the 3.5 mm size.
What are the maintenance and durability precautions?
Like any reusable surgical instrument, this Helmut Zepf elevator requires a rigorous decontamination, cleaning, and sterilization protocol after each use. Although resorption specificities do not apply here, the durability of the steel depends on compliance with autoclave sterilization cycles and the use of non-corrosive cleaning solutions. It is recommended to regularly inspect the condition of the 3.5 mm tip to detect any signs of wear, deformation, or corrosion. Proper maintenance ensures the preservation of the mechanical properties necessary for effective root luxation without compromising the integrity of the instrument.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a recognized company in the field of dental and surgical instrumentation. Regarding standards and regulatory classification, specific information is not detailed in the available technical documentation for this reference 17.201.02. However, Helmut Zepf products are generally designed according to high quality standards specific to medical devices produced in Germany. To obtain details on the CE marking, device class, or specific ISO certifications, it is imperative to refer to the instructions for use or labeling provided by the manufacturer at the time of purchase.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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