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Interchangeable Probe Tip Fig.25 - Helmut Zepf (24.099.25) - Delynov

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The Pointe interchangeable de sonde Fig.25 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.099.25.
  • Reserved for healthcare professionals. Read instructions carefully before use.

26.00 € 26.0 EUR 26.00 € Tax Included

26.00 € Tax Included

(26.00 € / Units)
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Instrument

What is the Helmut Zepf Fig.25 interchangeable probe tip?

The Fig.25 interchangeable tip, referenced under code 24.099.25, is a manual instrumentation component designed by Helmut Zepf Medizintechnik GmbH. This dental probe tip is manufactured from high-quality medical stainless steel, ensuring the necessary resistance to decontamination cycles. As a removable element, it attaches to a compatible probe handle to form a complete instrument. Its structure is specifically designed for the exploration of soft tissues and periodontal structures, offering the practitioner a modular solution for daily clinical examinations in the dental office or oral surgery.

What are the clinical indications for this periodontal probe tip?

This periodontal probe tip is indicated for the clinical evaluation of the condition of the tooth's supporting tissues. It is primarily used to measure the depth of the sulcus or periodontal pockets, detect the presence of subgingival calculus, and evaluate bleeding levels upon probing. In implantology, it allows for monitoring the health of peri-implant tissues. The use of this manual instrument is essential for establishing a precise periodontal diagnosis, monitoring the progression of inflammatory pathologies, and verifying the effectiveness of scaling and root planing treatments during follow-up visits.

What are the technical characteristics of reference 24.099.25?

The Fig.25 interchangeable tip (reference 24.099.25) is distinguished by its compatibility with the Helmut Zepf brand's interchangeable handle system. Manufactured in medical stainless steel, it features a geometry adapted for access to interproximal areas and deep pockets. Its design allows for rapid replacement of the working end without changing the entire instrument, thus optimizing instrument fleet management. Although delivered non-sterile, it is designed to withstand rigorous cleaning, disinfection, and autoclave sterilization protocols, in accordance with the maintenance requirements for reusable medical devices.

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

The main contraindication mentioned by the manufacturer Helmut Zepf concerns patients with a known hypersensitivity or intolerance to metals, particularly medical stainless steel. An allergic or hypersensitivity reaction may be triggered upon contact of the instrument with the mucous membranes. If such a reaction occurs during the examination, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, use is strictly reserved for qualified healthcare professionals mastering periodontal probing techniques to avoid any iatrogenic trauma to soft tissues or the epithelial attachment.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must undergo a complete reprocessing cycle before the first use and after each subsequent use. The protocol includes thorough cleaning, disinfection, and sterilization. It is crucial to visually inspect the graduated probe tip before each intervention to detect any potential damage such as cracks, breaks, or surface defects. Any instrument showing visible signs of wear or structural damage must never be used. Due to the quality of the materials used, there is no defined maximum limit of treatment cycles, as long as the functional integrity of the tip is preserved.

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 according to current regulations. Compliance with manufacturing standards ensures that the instrument meets safety and performance requirements for use in a clinical setting. Traceability is ensured by the technical reference 24.099.25. As a Class I device, it follows the conformity assessment procedures applicable to reusable manual dental instruments, thus providing dental surgeons with a reliable tool that complies with European medical quality standards.


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Manufacturer Helmut Zepf
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