Special Zepf-Bionik Curette, dental surgeon, bone graft and maxillo-facial surgery (24.204.15G) - Delynov
The Curette spéciale Zepf-Bionik , chirurgien-dentiste is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reference: 24.204.15G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Zepf-Bionik special curette (24.204.15G)?
The Zepf-Bionik special curette, referenced under code 24.204.15G by Helmut Zepf, is a manual instrument specifically developed for the needs of oral and implant surgery. Manufactured from medical stainless steel, this surgical dental curette features a structure adapted for precise handling in narrow areas of the oral cavity. As a device from Helmut Zepf, it meets the durability and performance requirements expected by practitioners for the treatment of soft tissues and sockets. This instrument belongs to the INSTRU category and benefits from a careful design by the manufacturer Helmut Zepf Medizintechnik Gmbh.
What are the clinical indications for this curette?
This surgical dental curette is indicated for use as a manual instrument during various odontological procedures. Its primary use concerns alveolar curettage after extraction, the elimination of inflammatory tissues or granulomas, and the cleaning of bone surfaces. It is particularly useful in periodontal surgery for pocket debridement or in the pre-implant phase to prepare the recipient site. The intended use, as defined by the manufacturer, is that of a manual dental instrument intended for qualified healthcare professionals working in clinical or hospital environments.
What are the technical characteristics of this instrument?
The Zepf-Bionik curette (reference 24.204.15G) is a reusable instrument designed in high-quality medical stainless steel. This material ensures the necessary resistance to repeated cleaning and sterilization cycles. The device is delivered non-sterile by the manufacturer and must undergo a complete disinfection and sterilization protocol before its first use, as well as between each patient. Its ergonomic design, specific to the Bionik range from Helmut Zepf, aims to optimize handling during delicate surgical movements, thus guaranteeing efficient transmission of force during curettage.
What are the contraindications for the use of this device?
The main medical contraindication mentioned by the manufacturer concerns known hypersensitivity or intolerance to metals, specifically to the medical stainless steel used for the manufacture of the instrument. If a hypersensitivity reaction is triggered in the patient upon contact, the surgical procedure must be immediately interrupted and necessary medical measures must be taken. It is the responsibility of the practitioner to check the patient's allergic history before the intervention. Furthermore, the use of an instrument showing visible damage, such as cracks or defects on the cutting edges, is strictly prohibited.
What are the maintenance and reprocessing precautions?
Like any reusable Class I instrument, this curette requires rigorous reprocessing. Before each use, the practitioner must visually inspect the product to detect any signs of wear, breakage, or corrosion. Damaged products must never be used. The treatment cycle includes cleaning, disinfection, and sterilization in accordance with current protocols. Due to the design and materials used, the manufacturer Helmut Zepf has not defined a maximum limit for treatment cycles, but the functional state of the instrument must be validated by the professional before each surgical act to ensure patient safety.
Who is the manufacturer and what standards are respected?
The Zepf-Bionik special curette is manufactured by Helmut Zepf Medizintechnik Gmbh, a recognized company located in Germany. This medical device is classified as Class I according to current regulations. The manufacturer guarantees the compliance of its production processes to meet safety and performance requirements. As a Class I device, it is intended exclusively for professional use by trained healthcare practitioners. Compliance with the maintenance and sterilization instructions issued by Helmut Zepf is essential to maintain the compliance of the device throughout its operational life within the dental practice.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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