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Pointed Curette. M4X0.5. - Helmut Zepf (24.751.102L) - Delynov

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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: 24.751.102L.
  • Reserved for healthcare professionals. Read instructions carefully before use.

31.60 € 31.6 EUR 31.60 € Tax Included

31.60 € Tax Included

(31.60 € / Units)
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Instrument

What is the Helmut Zepf curette tip?

The Helmut Zepf curette tip (reference 24.751.102L) is an interchangeable manual instrumentation component intended for periodontal care. Manufactured from medical stainless steel, it features a robust structure adapted to the mechanical stresses of oral surgery. Its particularity lies in its M4X0.5 thread connection system, allowing it to be fixed onto compatible handles from the same brand. This device is part of a modular approach to instrumentation, facilitating the replacement of the working part without changing the entire instrument. As a Helmut Zepf Medizintechnik GmbH product, it benefits from the expertise of a manufacturer recognized in the high-tech dental instrumentation sector.

What are the clinical indications?

This manual instrument is primarily indicated for periodontal and prophylaxis procedures. It is used by dental surgeons and periodontists for deep scaling and root planing. Its design allows access to subgingival areas to remove calcified deposits and necrotic tissue from dental root surfaces. The use of this curette tip is essential for treating periodontal pockets and promoting epithelial reattachment. It is also employed during maintenance phases to ensure the longevity of supporting tissues. The instrument is exclusively reserved for healthcare professionals trained in curettage and root debridement techniques.

What are the technical characteristics?

The Helmut Zepf curette tip is distinguished by its M4X0.5 precision thread, ensuring a stable and secure connection with the handle. Manufactured from a medical stainless steel selected for its cutting properties and corrosion resistance, it meets the requirements of surgical environments. The reference code 24.751.102L allows for precise identification of the model within the Helmut Zepf Medizintechnik GmbH manufacturer's range. The instrument is delivered non-sterile and requires a complete preparation protocol before any use. The design of the working part is optimized to provide effective access to complex anatomical sites while maintaining structural integrity during the application of curettage forces.

What are the contraindications for use?

The main medical contraindication mentioned by the manufacturer concerns known hypersensitivity or metal intolerance. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the procedure, the procedure must be stopped immediately and necessary clinical measures must be taken. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage or wear, such as cracks, breaks, or defects on the cutting edges. Using damaged products compromises patient safety and clinical treatment efficacy.

What are the maintenance and sterilization precautions?

Like all instruments from the Helmut Zepf brand, this curette tip must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The reprocessing process must be complete to guarantee asepsis. Before each use, the practitioner must carefully inspect the product for any signs of wear or degradation. Due to the design and materials used, there is no defined maximum limit for treatment cycles, but the functional state of the cutting edge should dictate its replacement. Preliminary cleaning is a critical step to remove all biological residues before the sterilization phase, in accordance with current hygiene protocols in the dental office.

Who is the manufacturer and what standards are met?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device (Class Ir according to MDR mentions), meeting safety and quality standards for manual instruments. The manufacturer specifies that compatibility with other products must be verified beforehand by the user. As a Class I instrument, it complies with European regulatory requirements relating to medical devices. Traceability is ensured by the technical reference 24.751.102L. Helmut Zepf is a manufacturer recognized for the precision of its instrumentation, guaranteeing healthcare professionals tools that comply with the most demanding clinical standards.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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