Shade. Octagonal handle. Figure 9 - Helmut Zepf (24.101.09) - Delynov
The Sonnette. Manche octogonal. Figure 9 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.101.09.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 24.101.09 curette?
The Helmut Zepf curette, referenced under code 24.101.09, is a specific manual instrument intended for oral surgery. This device is distinguished by its high-quality medical stainless steel structure, guaranteeing resistance to repeated sterilization processes. Its design includes an ergonomic octagonal handle, specifically studied to offer maximum stability and prevent the instrument from rolling between the practitioner's fingers. This design allows for optimal transmission of force during surgical movements. As a product of the manufacturer Helmut Zepf Medizintechnik GmbH, this instrument meets the rigorous manufacturing requirements for Class I devices.
What are the clinical indications for this instrument?
This instrument is indicated for use as a manual dental instrument during various oral surgery and implantology procedures. Although the manufacturer Helmut Zepf Medizintechnik GmbH does not list restrictive procedures, this type of curette (Figure 9) is classically used for cleaning sockets, removing granulomatous tissue, or preparing implant sites. Its use is strictly reserved for qualified healthcare professionals. It is used in curettage or tissue manipulation phases where the precision of the working tip is crucial for the success of the clinical procedure.
What are the technical characteristics of the 24.101.09 curette?
The Helmut Zepf 24.101.09 curette features technical characteristics focused on durability and precision. It is manufactured from medical stainless steel, selected for its mechanical properties and corrosion resistance. The octagonal handle is a major feature, providing a geometry that facilitates directional control of the instrument. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient. The absence of a defined maximum limit for treatment cycles underlines the robustness of its design, subject to regular visual inspection to detect any cracks or defects on the edges.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or metal intolerance. Since the instrument is composed of medical stainless steel, contact with the patient can trigger a hypersensitivity reaction in sensitive individuals. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures taken. Additionally, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects in the cutting edges, as this could compromise patient safety and the effectiveness of the surgical act.
What are the maintenance and reprocessing precautions?
The reprocessing of the Helmut Zepf curette must follow a strict protocol. Before the first use and after each subsequent use, the instrument must be cleaned, disinfected, and sterilized. It is imperative to check the condition of the stainless steel before each cycle: any worn or damaged product must never be reused. Due to its robust design and the materials used, the manufacturer has not defined a maximum limit for treatment cycles, but the longevity of the instrument depends directly on compliance with cleaning instructions. Compatibility with other cleaning and disinfection products must also be verified beforehand to avoid any premature degradation of the material.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer guarantees that the products are designed for professional use in a surgical environment. Although specific CE marking is not detailed in the provided technical data, compliance with manufacturing standards for medical stainless steel ensures conformity with safety requirements for manual instruments. Each instrument is identified by a unique technical reference (24.101.09) allowing precise traceability within the dental practice.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |