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Stone Burnisher 24.916.10

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The Pierre à Repasser 24.916.10 is a medical device manufactured by le fabricant.

  • Compliance: Medical device Class I.
  • Manufacturer: le fabricant.
  • Reserved for healthcare professionals. Read instructions carefully before use.

45.65 € 45.65 EUR 45.65 € Tax Included

45.65 € Tax Included

(45.65 € / Units)
  • Manufacturer

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Instrument

What is the 24.916.10 Helmut Zepf sharpening stone?

The 24.916.10 sharpening stone, marketed under the brand Helmut Zepf, is a device in the CONSO category designed for the maintenance of dental surgery instruments. Although exact material specifications are not detailed, this type of surgery sharpening stone is used to maintain the integrity of the sharp edges of manual instruments. This product is classified as a Class I device, meeting the basic regulatory requirements for non-invasive or reusable instruments after processing. Its role is fundamental for extending the lifespan of cutting tools in the dental office, thus ensuring consistent performance during clinical interventions.

What are the clinical indications for this sharpening stone?

The use of this dental sharpening stone is part of the maintenance of manual instruments used in odontology, particularly in periodontology and implant surgery. It is indicated for sharpening cutting edges that show damage or visible wear, such as cracks or breaks. According to the guidelines from the manufacturer Helmut Zepf Medizintechnik Gmbh, it is crucial to check the condition of instruments before each use. Regular application of an arkansas surgery stone or a similar model allows for the preservation of the precision necessary for curettage or resection procedures, thus avoiding the use of damaged or dull products that could compromise patient safety.

What are the technical characteristics of the 24.916.10 stone?

The 24.916.10 stone from Helmut Zepf is characterized by its function as a manual sharpening stone intended for healthcare professionals. As a Class I device, it is delivered non-sterile by the manufacturer. Its design is optimized for reprocessing, although no maximum limit of processing cycles can be defined due to the nature of the materials and the intended use. It must be cleaned, disinfected, and sterilized before the first use and after each subsequent cycle. It is imperative to visually inspect the condition of the stone to detect any defects on the active surfaces in order to guarantee a homogeneous and safe sharpening of surgical instruments.

What are the contraindications for the use of this device?

The major contraindications related to the use of instruments maintained with this device primarily concern known hypersensitivity to metals. The manufacturer specifies that metal intolerance, particularly medical stainless steel, can trigger hypersensitivity reactions in certain patients upon contact with the instrument. If such a reaction occurs during the procedure, it must be immediately stopped and the necessary medical measures must be taken. Furthermore, the use of the stone is strictly reserved for qualified healthcare professionals, and it is formally prohibited to use products showing visible damage such as cracks or breaks.

What are the maintenance and sterilization precautions?

The reprocessing protocol for Helmut Zepf products requires complete cleaning, disinfection, and sterilization before any use. The 24.916.10 sharpening stone must be integrated into the office's instrument management cycle. Before each use, a meticulous inspection is required to identify any wear or defects on the cutting edges. Compatibility with other cleaning and sterilization products must be verified beforehand by the practitioner. As it is a reusable instrument with no defined cycle limit, the professional's vigilance regarding the physical state of the device is the primary criterion for remaining in service or disposal.

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. The product complies with the regulations for Class I medical devices (Class Ir according to certain technical specifications from the manufacturer). The products are delivered non-sterile and must undergo a full preparation cycle before clinical use. The manufacturer insists that these instruments are exclusively reserved for professional use by healthcare practitioners. Compliance with instructions for use and safety, including systematic cleaning before the first commissioning, is mandatory to guarantee compliance with current health safety standards.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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