Frontal Teeth Curette - Helmut Zepf (24.751.130) - Delynov
The Curette pour dents frontales - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.130.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf curette for frontal teeth?
The Helmut Zepf curette for frontal teeth, referenced under code 24.751.130, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, it is specifically structured to access the surfaces of the anterior teeth. This device belongs to Class I of medical devices. Its design allows for rigorous handling during periodontal care. As a non-sterile instrument upon delivery, it requires a complete cycle of cleaning, disinfection, and sterilization before its first use in the office or operating theater, thus ensuring the safety of the patient and the practitioner.
What are the clinical indications for this instrument?
This manual instrument is indicated for periodontology and dental hygiene procedures, specifically for the frontal sector. Its primary use lies in deep scaling and root planing. It effectively removes calcified deposits and granulomatous tissue in the periodontal pockets of incisors and canines. The use of this Helmut Zepf curette is strictly reserved for qualified healthcare professionals. It is used in maintaining gingival health and preparing tissues before more complex oral or implant surgery interventions, ensuring optimal decontamination of root surfaces.
What are the technical characteristics of the 24.751.130 curette?
The Helmut Zepf 24.751.130 curette is characterized by its manufacture in high-quality medical stainless steel, offering the necessary resistance to repeated reprocessing cycles. Its morphology is adapted to the anatomy of the frontal teeth, facilitating correct angulation against the root. Before each use, the practitioner must imperatively inspect the instrument to detect any visible damage such as cracks, breaks, or defects on the cutting edges. The use of a worn or damaged instrument is prohibited to maintain the effectiveness of the clinical gesture. Its design allows for thorough cleaning, although there is no defined maximum limit of processing cycles, as this depends on the actual wear observed during inspection.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this Helmut Zepf curette is the patient's known hypersensitivity or intolerance to metals, particularly medical stainless steel. An allergic reaction may occur during contact between the instrument and the patient's tissues. If such a hypersensitivity reaction is triggered during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to question the patient about their allergic history before any manipulation. Additionally, the instrument must never be used if it shows signs of wear or visible structural defects that could compromise the safety of care.
What are the cleaning and sterilization precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. A strict reprocessing protocol is mandatory before the first use and after each subsequent use. This includes complete cleaning, disinfection, and sterilization. It is crucial to check the compatibility of this instrument with other cleaning products and devices used. Due to its stainless steel design, the instrument must be inspected after each cycle to verify the integrity of the sharp edges. Any defect on the cutting edges makes the instrument unfit for use. The lifespan of the instrument depends on the intended use and the rigor of the maintenance process performed by the healthcare professional.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with strict regulatory requirements for the production of manual dental instruments in medical stainless steel. Each product, such as the 24.751.130 curette, is subject to rigorous quality controls before being placed on the market. As a recognized manufacturer, Helmut Zepf guarantees that its instruments are suitable for professional use in a clinical setting, provided that the maintenance and safety instructions specified in the technical documentation are respected.
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Specifications
| Manufacturer | Helmut Zepf |
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