Curette Tip M4X0.5 - Helmut Zepf (24.751.113C)
The Pointe de Curette M4X0.5 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.113C.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf M4X0.5 curette tip?
The M4X0.5 curette tip, referenced under code 24.751.113C by the manufacturer Helmut Zepf Medizintechnik GmbH, is an interchangeable manual dental instrument. Made of medical stainless steel, this tip is intended to be mounted on a compatible instrumentation handle via a specific thread. Its structure is optimized for curettage and root surface cleaning procedures in periodontal surgery. As a component of a modular system, it allows the practitioner to replace only the working part of the instrument, thus ensuring constant cutting efficiency while optimizing instrument inventory management within the dental practice.
What are the clinical indications for this instrument?
This manual instrument is indicated for periodontology and prophylaxis procedures. Its primary use concerns the removal of subgingival calculus, root planing, and the elimination of infected soft tissue during gingival curettage. The design by Helmut Zepf allows for targeted intervention in periodontal pockets to promote epithelial reattachment. It can also be used during pre-implant surgery or peri-implantitis treatments to sanitize the concerned sites. Its use is strictly reserved for qualified healthcare professionals mastering manual curettage techniques and associated asepsis protocols.
What are the technical characteristics of the 24.751.113C tip?
The Helmut Zepf 24.751.113C curette tip is characterized by its manufacture in medical-grade stainless steel, guaranteeing corrosion resistance during sterilization cycles. It features an M4X0.5 thread for secure attachment to instrument handles of the same range. The manufacturer emphasizes the importance of checking the condition of the cutting edges before each intervention. Any visible damage, such as cracks, breaks, or defects on the sharp edges, must lead to the immediate withdrawal of the product. Like all products from the Helmut Zepf Medizintechnik GmbH brand, this tip is delivered non-sterile and requires a complete processing protocol before its first use.
What are the contraindications for using this curette?
The main medical contraindication documented by the manufacturer Helmut Zepf concerns hypersensitivity or metal intolerance. Since the instrument is made of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the clinical act, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows obvious signs of wear, deformations, or dull cutting edges, as this could compromise patient safety and treatment efficacy.
What are the maintenance and sterilization precautions?
Helmut Zepf products are delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. It is crucial to thoroughly clean each tip to remove any organic residue before autoclaving. Due to its technical design and the materials used, the manufacturer specifies that there is no defined maximum limit for processing cycles, provided that the functional integrity of the instrument is preserved. The practitioner must systematically check compatibility with other products and verify the absence of cracks or breaks before any insertion into the mouth.
Who is the manufacturer and what standards are met?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This product belongs to Class I (Class Ir according to certain reprocessing nomenclatures) of medical devices. Manufacturing complies with the rigorous quality standards imposed for manual stainless steel dental instrumentation. As a Class I device, it meets the current regulatory safety and performance requirements for non-invasive or invasive surgical instruments for temporary use. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to guarantee the device's conformity throughout its operational life.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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