ZEPF-BIONIK. CURETTE SPECIALE - Helmut Zepf
The Curette spéciale Zepf-Bionik - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.207.17G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Zepf-Bionik special curette - Helmut Zepf (24.207.17G)?
The Zepf-Bionik special curette, referenced under code 24.207.17G by the manufacturer Helmut Zepf, is a precision manual instrument intended for odontological use. Designed in high-quality medical stainless steel, this specific periodontal curette is structured to meet the requirements of clinical periodontology interventions. Its design allows access to complex anatomical areas for thorough cleaning. As a device from the Helmut Zepf brand, it benefits from the expertise of Helmut Zepf Medizintechnik GmbH in the manufacture of surgical instruments. This device is delivered non-sterile and requires rigorous preparation before any use in the office or operating theater.
What are the clinical indications for this instrument?
This instrument is primarily indicated as a root planing instrument within the framework of periodontal therapies. It is used by dental surgeons and periodontists for the removal of calculus and dental plaque located in hard-to-reach subgingival areas. The specific gracey curette allows for effective debridement of tooth roots, thus promoting epithelial reattachment and the reduction of periodontal pockets. Its use is strictly reserved for qualified healthcare professionals involved in the treatment of periodontitis or during complex periodontal maintenance phases requiring fine instrumentation adapted to the root morphology.
What are the technical characteristics of the 24.207.17G curette?
The Zepf-Bionik special curette is distinguished by its medical stainless steel construction, guaranteeing the resistance necessary for the mechanical stresses of scaling. The reference code 24.207.17G identifies a specific geometry of the working part, optimized for precise dental segments. This instrument belongs to the INSTRU category and meets Class I standards according to medical device regulations. Its design allows for optimal tactile transmission for the practitioner during the removal of calcified deposits. Like all Helmut Zepf products, this instrument is reusable after a full reprocessing cycle, including cleaning, disinfection, and steam sterilization, in accordance with current protocols.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If a hypersensitivity reaction occurs during the procedure, the intervention must be immediately interrupted and necessary medical measures must be initiated. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the treatment.
What are the maintenance and sterilization precautions?
Helmut Zepf instruments are delivered non-sterile and must undergo a full cycle of cleaning, disinfection, and sterilization before the first use, and then between each patient. Before each use, the practitioner must carefully inspect the curette to detect any signs of wear or corrosion. Due to the design of the instrument and the materials used, there is no defined maximum limit for treatment cycles; however, the use of damaged or worn products is prohibited. Compatibility with other cleaning products and sterilization devices must be verified beforehand to maintain the integrity of the stainless steel.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device belongs to Class I (Class Ir according to the manufacturer's specific mentions) in accordance with European regulations on medical devices. Compliance with rigorous manufacturing protocols by Helmut Zepf ensures the conformity of the instrument for professional use in surgical and dental environments. As a manual instrument, it meets the safety and performance requirements for non-invasive or temporary-use invasive medical devices, thus guaranteeing constant reliability during periodontology and planing procedures.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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