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Dental Surgery Figurine 125/126 - Helmut Zepf (24.708.25) - Delynov

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The Excavateur Figurine 125/126 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.708.25.
  • Reserved for healthcare professionals. Read instructions carefully before use.

38.89 € 38.89 EUR 38.89 € Tax Included

38.89 € Tax Included

(38.89 € / Units)
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Instrument

What is the Figurine 125/126 excavator - Helmut Zepf?

The Figurine 125/126 excavator, referenced under code 24.708.25, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is specifically developed for operative dentistry interventions. It consists of a central shaft and two working ends configured according to 125/126 standards. This device belongs to the category of reusable consumables after a strict cleaning and sterilization protocol. As a Class I instrument, it meets the safety requirements for non-invasive or short-term invasive medical devices used in dental practices.

What are the clinical indications for this excavator?

The intended use of this Helmut Zepf instrument is that of a classic manual dental instrument. In clinical practice, it is primarily indicated for the removal of softened dentin during the treatment of carious lesions. It allows the practitioner to eliminate infected tissues in a controlled manner, thus preserving the surrounding healthy dental structure. It is also used for cleaning cavities, removing temporary filling materials, or shaping cavity walls before placing a permanent restorative material. Its application is strictly reserved for health professionals qualified in dental surgery and oral care.

What are the technical characteristics of reference 24.708.25?

The Helmut Zepf excavator (ref. 24.708.25) is distinguished by its manufacture in high-quality medical stainless steel, guaranteeing resistance to repeated sterilization cycles. The double-ended design (Figurine 125/126) offers versatility when accessing different tooth surfaces. Although delivered non-sterile, the instrument is designed to withstand complete reprocessing protocols including cleaning, disinfection, and steam sterilization. The manufacturer emphasizes the importance of checking the integrity of the instrument before each use, particularly the absence of cracks, breaks, or visible defects on the cutting edges, to guarantee optimal clinical performance.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. Since the instrument is manufactured from medical stainless steel, contact with the patient's tissues may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore recommended to question the patient about their allergic history before any manipulation. Apart from this material-related specificity, use is contraindicated if the instrument shows damage or visible wear.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The reprocessing process must be complete to guarantee asepsis. Before proceeding with sterilization, the practitioner must visually inspect the excavator for any cracks or deformations. Due to the robust design and materials used, there is no defined maximum limit of treatment cycles, as long as the instrument maintains its physical integrity and cutting capabilities. The use of a damaged or worn product is strictly prohibited to avoid any risk of breakage or tissue trauma.

Who is the manufacturer and what standards are respected?

This excavator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. The device is classified as Class I (Class Ir according to certain conformity mentions related to reprocessing) in accordance with medical device regulations. Manufacturing follows rigorous standards to ensure compatibility with other products in the Helmut Zepf catalog. Compliance with cleaning and sterilization protocols is essential to maintain the conformity of the instrument during its use in a clinical setting. This product is exclusively intended for professional use by health practitioners trained in dental techniques.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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