Round 3mm Elevator - Helmut Zepf (17.020.02) - Delynov
The Élévateur rond de 3 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.020.02.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 3 mm round elevator?
The 3 mm round elevator, reference 17.020.02, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is specifically developed for oral surgery interventions requiring effective mobilization of roots or teeth. Its round working part with a 3 mm diameter allows for precise insertion into the alveolar space. As a Class I device, it meets the quality requirements for professional use in dental practices or hospital environments. This instrument is delivered non-sterile and requires a complete cleaning and sterilization protocol before its first use and between each patient.
What are the clinical indications for this 3mm elevator?
The use of this 3mm dental elevator is primarily indicated during the initial phases of dental extraction. It is used to luxate the tooth by exerting controlled pressure to break the periodontal ligament fibers. Its 3 mm round geometry is particularly suited for insertion between the root and the alveolar bone, thus facilitating the elevation of the dental structure. It is used by dental surgeons and implantologists in single extraction procedures, residual roots, or during the preparation of an alveolar site before immediate implant placement. Its role is crucial for minimizing trauma to the surrounding bone walls during luxation.
What are the technical characteristics of the 17.020.02 instrument?
The Helmut Zepf round dental elevator is distinguished by its robust design in high-quality medical stainless steel. Technical reference 17.020.02 corresponds to a model equipped with an active tip of 3 mm in diameter, optimized for force transmission during leverage. The structure of the instrument is designed to withstand repeated mechanical stress during luxation cycles. The manufacturer Helmut Zepf Medizintechnik GmbH ensures a finish that allows for thorough cleaning and disinfection. As specified in the technical documentation, the design and materials used do not allow for the definition of a maximum limit of processing cycles, although the condition of the instrument (cracks, breaks, defects) must be checked before each use.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns patients with a known intolerance or hypersensitivity to metals, particularly the medical stainless steel used for the manufacture of the instrument. In the event of a hypersensitivity reaction triggered during contact with the elevator, the surgical procedure must be immediately interrupted and the necessary medical measures must be taken. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage such as cracks, breaks, or defects on the edges, as this could compromise patient safety and the effectiveness of the surgical gesture.
What are the maintenance and sterilization precautions?
Helmut Zepf products are delivered non-sterile. It is imperative to perform complete cleaning, disinfection, and sterilization before the first use, as well as after each intervention. The reprocessing process must be rigorous: each product must be inspected for any visible wear or damage before use. The use of damaged or worn products is prohibited. Due to the nature of the materials and the intended use, there is no predetermined maximum number of sterilization cycles, but the practitioner's vigilance is required to assess the integrity of the instrument. Compatibility with other products used during reprocessing must also be verified beforehand.
Who is the manufacturer and what standards are respected?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Germany in Seitingen-Oberflacht. This medical device belongs to Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with the safety and traceability protocols in force for manual dental instruments. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to guarantee the longevity of the tool and the safety of care. The use of this elevator is strictly reserved for qualified healthcare professionals trained in oral surgery techniques and sterilization protocols for reusable medical devices.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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