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ARKANSAS. PIERRE A AFFUTER. - Helmut Zepf

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The Pierre à Affûter Arkansas - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.914.25.
  • Reserved for healthcare professionals. Read instructions carefully before use.

62.24 € 62.24 EUR 62.24 € Tax Included

62.24 € Tax Included

(62.24 € / Units)
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Instrument

What is the Arkansas Sharpening Stone - Helmut Zepf?

The Arkansas sharpening stone, referenced under code 24.914.25 by the manufacturer Helmut Zepf, is a maintenance tool designed for manual instrumentation. This product belongs to the category of technical consumables for the dental office. It is presented as a block of high-density natural or synthetic stone, specifically selected for its ability to rectify medical stainless steels. Its main role is to restore the sharpness of surgery and periodontics instruments, thus guaranteeing optimal cutting performance during clinical interventions. It is delivered non-sterile and must be integrated into the practitioner's instrumentation management protocol.

What are the clinical indications for this sharpening accessory?

The use of the Helmut Zepf Arkansas stone is indicated for the regular maintenance of manual instruments used in oral surgery and periodontal care. Its direct application concerns the rectification of cutting edges dulled by use and sterilization cycles. By maintaining a precise edge on curettes, scalers, or surgical scissors, this accessory promotes clean and controlled clinical movements. The manufacturer specifies that this manual instrument is intended for use by qualified healthcare professionals capable of identifying visible damage such as cracks or defects on the sharp edges before any care procedure.

What are the technical characteristics of the stone 24.914.25?

The Helmut Zepf Arkansas sharpening stone (reference 24.914.25) is distinguished by its fine grain, suitable for finishing medical steels. Although delivered non-sterile, it must undergo rigorous cleaning before its first use. Its design allows for precise interaction with stainless steel instruments. It is imperative to check compatibility with other products before use. The manufacturer emphasizes that due to the nature of the product and its intended use, there is no defined maximum limit for processing cycles, although visible wear must lead to the immediate replacement of the accessory to avoid any risk during handling.

What are the contraindications for the use of this device?

The major contraindications mentioned by Helmut Zepf Medizintechnik GmbH mainly concern hypersensitivity reactions. Although the stone is a maintenance tool, contact of the sharpened instrument (made of medical stainless steel) with the patient can cause metal intolerance. If such a hypersensitivity reaction is triggered, the clinical procedure must be immediately interrupted and necessary measures must be taken. Furthermore, it is strictly forbidden to use products showing visible damage, cracks, or breaks. Use is strictly reserved for healthcare professionals trained in the maintenance techniques of surgical instrumentation.

What are the maintenance and sterilization precautions?

All products supplied by Helmut Zepf, including this sharpening stone, are delivered non-sterile. They must imperatively be cleaned, disinfected, and sterilized before the first use, as well as before each subsequent use. The reprocessing process must be complete. It is crucial to visually inspect the stone to detect any trace of wear, cracks, or defects on the working surfaces. The use of a damaged product is prohibited. The manufacturer does not impose a predefined cycle limit, but the practitioner's vigilance regarding the structural state of the accessory is decisive in guaranteeing the safety and effectiveness of the sharpening of surgical instruments.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). It meets the regulatory requirements for manual dental instruments. The manufacturer ensures the traceability and compliance of its products intended for healthcare professionals. As a Class I device, it respects the safety and performance standards necessary for its integration into a surgical and odontological environment, provided that the cleaning and sterilization protocols recommended by Helmut Zepf are rigorously applied by the end user.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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