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White. Excavator. Figure 18 - Helmut Zepf (24.733.18) - Delynov

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The Blanc. Excavateur. Figure 18 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.733.18.
  • 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 Excavator Figure 18 Helmut Zepf?

The Excavator Figure 18, referenced under code 24.733.18, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device belongs to the category of consumables for dental surgery and conservative care. Manufactured from medical stainless steel, this instrument is specifically developed to withstand the cleaning, disinfection, and sterilization protocols required in a dental office. Its structure is adapted for handling dental tissues during cavity preparation phases, providing practitioners with a reliable tool for treating carious pathologies.

What are the clinical indications for this instrument?

According to data from the manufacturer Helmut Zepf, this instrument is indicated as a manual dental instrument. In clinical practice, the Excavator Figure 18 is primarily used for caries removal, allowing for the eviction of softened dentin and food debris within a cavity. It is also employed for the application or removal of temporary dressing materials. Its use is reserved exclusively for qualified healthcare professionals performing curative dental care where precise manual intervention is necessary to preserve healthy dental structures while eliminating infected tissue.

What are the technical characteristics of excavator 24.733.18?

The Helmut Zepf excavator (reference 24.733.18) is characterized by its high-quality medical stainless steel composition. It is delivered non-sterile and requires a complete reprocessing cycle (cleaning, disinfection, and sterilization) before its first use and after each subsequent use. The manufacturer states that due to its robust design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, although the instrument must be visually inspected before each intervention. Any sign of visible damage, such as cracks, breaks, or defects on the cutting edges, must lead to the immediate removal of the product from clinical use.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns metal intolerance. A hypersensitivity reaction in the patient may occur upon contact with the medical stainless steel composing the instrument. If such an allergic reaction or intolerance is suspected or occurs during the operative procedure, the procedure must be stopped immediately. Necessary medical measures must then be taken accordingly to ensure patient safety. It is therefore recommended to check the patient's allergic history before any intervention with manual metallic instruments.

What are the maintenance and safety precautions?

Like any instrument from the Helmut Zepf brand, this excavator must be cleaned, disinfected, and sterilized before the first use. It is imperative to check the condition of the instrument before each use to detect any potential wear or visible damage, particularly on the active cutting parts. The use of damaged products or those showing cracks is strictly prohibited. Additionally, compatibility with other products used during the procedure must be verified beforehand. Compliance with these safety instructions guarantees not only the longevity of the instrument but also the essential aseptic safety during clinical care.

Who is the manufacturer and what standards are met?

This excavator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. The product is classified as a Class I medical device according to current regulations. It meets strict manufacturing requirements for manual instruments made of medical stainless steel. Reprocessing protocols must follow standard sterilization guidelines to maintain the compliance and safety of the device. As a Class I device, it is intended for strict professional use in the field of oral health, respecting German industrial quality standards.


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Manufacturer Helmut Zepf
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