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Curette Tip. M4X0.5. - Helmut Zepf (24.751.105L)

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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: 24.751.105L.
  • 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 24.751.105L curette tip?

The Helmut Zepf curette tip, referenced under code 24.751.105L, is an interchangeable manual dental instrument designed for periodontal and surgical care. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this tip features a specific M4X0.5 thread allowing it to be mounted on a compatible handle. Its structure is designed to provide a precise tactile response during curettage procedures. This device is delivered non-sterile and must undergo a full cleaning, disinfection, and sterilization cycle before its first use in the practice, in accordance with current hospital hygiene protocols.

What are the clinical indications?

This instrument is indicated as a manual dental instrument for oral surgery and periodontology procedures. It is primarily used for the removal of subgingival calculus, root planing, or debridement of granulation tissue in sockets or implant sites. Its use is strictly reserved for qualified healthcare professionals. The practitioner must check the integrity of the instrument before each procedure, ensuring the absence of cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is prohibited to guarantee patient safety and the effectiveness of the surgical procedure.

What are the technical characteristics?

The Helmut Zepf 24.751.105L curette tip is distinguished by its M4X0.5 threaded connection system, ensuring stable fixation on handles from the same range. It is designed in medical stainless steel, a standard material for surgical instrumentation due to its resistance to repeated sterilization cycles. As a Class I device, it meets the basic regulatory requirements for non-invasive or invasive manual instruments for temporary use. The manufacturer does not define a maximum limit of processing cycles, as this depends directly on visible wear, product design, and compliance with maintenance instructions specific to rotary or manual instruments.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. Contact with this medical stainless steel instrument may trigger an allergic reaction in certain sensitive patients. If such a hypersensitivity reaction occurs during the operative act, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to question the patient about their allergic history before any intervention. Additionally, use is contraindicated if the instrument shows visible damage such as cracks or blunt edges that could compromise clinical safety.

What are the maintenance and reprocessing precautions?

Helmut Zepf products are delivered non-sterile. Before the first use and after each procedure, the curette tip must be cleaned, disinfected, and sterilized. The cleaning process must be meticulous to remove all organic residues before autoclaving. Due to its design and the materials used, there is no predefined maximum number of sterilization cycles; the end of the instrument's life is determined by the appearance of signs of wear or corrosion. It is imperative to check compatibility with other products (handles) before use. Any instrument showing defects on the active parts or at the thread level must be discarded immediately.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing nomenclatures). As a recognized manufacturer in the dental instrumentation sector, Helmut Zepf ensures the traceability and compliance of its products with European regulatory requirements relating to medical devices. The 24.751.105L curette tip complies with manufacturing standards for stainless steel manual instruments. Compliance with the safety and use instructions provided by the manufacturer is mandatory to maintain conformity and guarantee patient safety during care.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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