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Curette Tip, M4x0.5 - Helmut Zepf (24.751.204R) - 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: 24.751.204R.
  • 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 (24.751.204R)?

The Helmut Zepf curette tip, reference 24.751.204R, is an interchangeable manual dental instrument designed for the practice of periodontics and oral surgery. This device is manufactured from medical stainless steel, a standard material ensuring the rigidity necessary for curettage procedures. It is distinguished by its specific M4X0.5 connection system, allowing the tip to be fixed onto a compatible instrument holder handle. As a manual instrument, it is intended for strict professional use in dental offices or hospital environments. This product is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH and requires a complete preparation protocol before any clinical use on a patient.

What are the clinical indications for this instrument?

This periodontics curette tip is indicated for periodontal debridement procedures and minor oral surgery. Its primary use involves the removal of deep calculus and the cleaning of root surfaces (planing) to treat periodontal pockets. In surgery, this dental curette tip may be used for the enucleation of inflammatory or granulation tissues. The practitioner must verify the compatibility of this tip with their existing handles before the intervention. The instrument is designed to provide a precise tactile response during the removal of calcified deposits or pathological tissues, thereby contributing to the patient's periodontal health as part of a global treatment plan.

What are the technical characteristics of this tip?

Technically, this Helmut Zepf instrument is characterized by an M4X0.5 type thread, ensuring stable and secure fixation on the handle. Its medical stainless steel composition provides resistance adapted to the mechanical stresses of manual curettage. The manufacturer specifies that the product is delivered non-sterile and that it is the responsibility of the healthcare professional to proceed with cleaning, disinfection, and sterilization before the first use, as well as after each care cycle. Before each use, a visual inspection is mandatory to detect potential damage such as cracks, breaks, or wear of the cutting edges, as the use of damaged products is strictly prohibited to guarantee the safety of care.

What are the contraindications for the use of this curette tip?

The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. As the instrument is manufactured from medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Apart from this material-related contraindication, the use of the instrument is reserved exclusively for qualified healthcare professionals mastering periodontal curettage techniques, in order to avoid any iatrogenic damage to dental or gingival structures.

What are the maintenance and reprocessing precautions?

The reprocessing of this dental curette tip follows a rigorous protocol. All instruments must be cleaned, disinfected, and sterilized before their first commissioning and after each subsequent use. Due to the product design and the materials used, there is no defined maximum limit for the number of treatment cycles, as long as the instrument does not show visible signs of wear. It is crucial to carefully clean each product to remove any organic residue before sterilization. The practitioner must be particularly attentive to the condition of the cutting edges and the integrity of the M4X0.5 thread. Any instrument showing surface defects or a loss of cutting efficiency must be removed from service.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. The product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). It meets the regulatory requirements for reusable manual dental instruments. Traceability is ensured by the catalogue reference 24.751.204R. The manufacturer emphasizes that its products are intended exclusively for healthcare professionals. Compliance with cleaning and sterilization protocols is the responsibility of the dental office, in accordance with the instructions provided by Helmut Zepf to guarantee patient safety and the longevity of the stainless steel instrumentation.


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Manufacturer Helmut Zepf
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