Skip to Content

Curette Tip. M4X0.5. - Helmut Zepf (24.751.109G)

https://www.delynov.fr/web/image/product.template/9626/image_1920?unique=e546a94

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: 24.751.109G.
  • 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)
  • Manufacturer

This combination does not exist.

Instrument

What is the Helmut Zepf 24.751.109G CURETTE TIP?

The curette tip referenced 24.751.109G is a manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this active part is intended to be mounted on a compatible handle via its M4X0.5 thread. Its structure is specifically designed for periodontology and prophylactic hygiene interventions. As a Class I device, it meets quality requirements for repeated use in the practice after a strict sterilization protocol. This component is delivered non-sterile and must undergo complete processing before its first use.

What are the clinical indications for this instrument?

This Helmut Zepf manual instrument is primarily indicated for cleaning and smoothing root surfaces. In oral and periodontal surgery, it enables effective removal of subgingival calculus and debridement of infected soft tissues within periodontal pockets. Its use also extends to peri-implant maintenance to ensure the sanitation of surgical sites. The instrument helps restore gingival health by facilitating access to complex anatomical areas thanks to its curette morphology. It is exclusively reserved for use by qualified healthcare professionals in dentistry and oral surgery.

What are the technical characteristics of the 24.751.109G tip?

The Helmut Zepf curette tip is distinguished by its standardized M4X0.5 thread, ensuring a stable and secure connection with handles from the corresponding range. It is crafted from a medical stainless steel selected for its mechanical resistance during curettage forces. The manufacturer specifies that the instrument must be visually inspected before each use to detect potential damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to guarantee the effectiveness of the clinical gesture and patient safety.

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. Contact of the medical stainless steel instrument with patient tissues may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the operative procedure, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any intervention with this manual instrument.

What are the maintenance and sterilization precautions?

As Helmut Zepf products are delivered non-sterile, a rigorous reprocessing protocol is mandatory. Before the first use and after each clinical act, the curette tip must be cleaned, disinfected, and sterilized. The manufacturer emphasizes the importance of fully cleaning each product to remove all biological residues. Due to the design of the instrument and the materials used, there is no defined maximum limit for treatment cycles, as long as the physical integrity of the cutting edge and the thread is preserved. Any visible sign of wear must lead to the immediate replacement of the tip.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer in the dental instrumentation sector ensures the compliance of this product with the regulation for Class I medical devices. Although the specific CE marking is not detailed in the provided sources, the instrument is classified as Class Ir (MDC0483) according to safety directives. Compatibility with other products of the Helmut Zepf system must be verified by the practitioner before use to ensure assembly compliant with surgical safety standards.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
Tags
Tags
Instrument