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GILLET. EXCAVATEUR. DOUBLE. FIG. 244 - Helmut Zepf

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The Excavateur double Gillet, figure 244 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.711.44.
  • Reserved for healthcare professionals. Read instructions carefully before use.

44.43 € 44.43 EUR 44.43 €excl. VAT

44.43 €excl. VAT

(44.43 € / Units)
  • Manufacturer

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Instrument
Manufacturer: Helmut Zepf

What is the Helmut Zepf Gillet double excavator?

The Gillet double excavator, figure 244, bearing reference 24.711.44, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This instrument is designed in medical stainless steel, a material chosen for its resistance to repeated sterilization cycles in clinical environments. As a dental double excavator, it features two symmetrical active ends that allow the practitioner to intervene on different faces of the tooth without changing instruments. This device belongs to the category of reusable consumables and is classified as a Class I medical device, meeting the safety requirements for non-invasive manual instrumentation in dental surgery.

What are the clinical indications for this instrument?

This instrument is indicated for restorative dentistry and conservative surgery procedures. Its primary role is the removal of carious dentin and the cleaning of dental cavities. The practitioner uses the sharp edges of the excavator to remove dentinal tissue softened by the carious process while preserving the healthy structure. It is also useful for removing temporary filling materials or for shaping cavity floors. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons, within the framework of routine dental care or pre-prosthetic preparations.

What are the technical characteristics of reference 24.711.44?

The Gillet double excavator (24.711.44) is distinguished by its double-ended configuration, optimized for manual handling. Manufactured by Helmut Zepf, it benefits from a high-quality medical stainless steel design, ensuring the longevity of its cutting edges. The design of figure 244 is specifically studied to offer ergonomic access to hard-to-reach areas. Before each use, the practitioner must imperatively inspect the instrument to detect any visible damage, such as cracks, breaks, or defects on the sharp parts. The use of damaged or worn products is prohibited to guarantee the effectiveness of the clinical gesture.

What are the contraindications for using this excavator?

The main medical contraindication identified by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, particularly to the components of medical stainless steel. If a hypersensitivity reaction occurs in the patient upon contact with the instrument, the procedure must be immediately interrupted and necessary medical measures must be taken. There are no other specific contraindications mentioned, as long as the instrument is used in accordance with its intended use as a manual device for dental surgery and by qualified personnel respecting the usage protocols.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. Reprocessing must follow rigorous protocols to guarantee asepsis. Due to its design and the materials used, there is no defined maximum limit of treatment cycles, but natural wear must be monitored. It is crucial to clean each product before proceeding with sterilization to avoid the fixation of organic residues. Compatibility with other cleaning and disinfection products must also be verified beforehand by the dental office.

Who is the manufacturer and what standards are respected?

The Gillet double excavator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device complies with current regulations and is classified as Class I (Class Ir according to the MDC0483 repository for reusable instruments). The manufacturer imposes high quality standards for the production of its manual stainless steel instruments. As a Class I device, it meets the essential safety and performance requirements. Compliance with the maintenance and sterilization instructions issued by Helmut Zepf is essential to maintain product compliance throughout its operational life.


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