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Root Canal File 0.6 mm - Helmut Zepf (19.512.06) - Delynov

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The Fouloir de canal radiculaire 0.6 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.512.06.
  • Reserved for healthcare professionals. Read instructions carefully before use.

47.68 € 47.68 EUR 47.68 € Tax Included

47.68 € Tax Included

(47.68 € / Units)
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Instrument

What is the Helmut Zepf 0.6 mm root canal plugger?

The 0.6 mm root canal plugger, referenced under code 19.512.06 by Helmut Zepf, is a manual instrument designed for endodontics. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device is intended for the condensation of filling materials inside root canals. Its rigid structure and calibrated tip allow the practitioner to exert controlled pressure to compact materials such as gutta-percha. This device belongs to Class I of medical devices, guaranteeing its compliance with safety requirements for non-invasive or short-term invasive manual instruments in dental surgery.

What are the clinical indications?

This instrument is indicated for endodontic filling procedures, specifically for hot or cold vertical condensation. In dental surgery and endodontics, it is used to push back and compact filling materials to eliminate voids and ensure a perfect seal of the root canal after its preparation. Its 0.6 mm diameter makes it particularly useful for working in medium-sized canals or during intermediate condensation phases. The use of this Helmut Zepf instrument is strictly reserved for qualified healthcare professionals in the context of conservative care or root canal treatments prior to prosthetic restoration.

What are the technical characteristics?

The Helmut Zepf plugger (reference 19.512.06) features a tip diameter of 0.6 mm. It is designed in medical stainless steel, a material chosen for its resistance to corrosion and its ability to withstand repeated reprocessing cycles. As a Class I instrument, it meets the manufacturing standards of Helmut Zepf Medizintechnik GmbH. The product is delivered non-sterile, which requires a strict protocol of cleaning, disinfection, and sterilization before the first use and between each patient. Its ergonomic design allows for direct transmission of the axial force necessary for compacting endodontic materials without unwanted bending of the shaft.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient can trigger allergic or hypersensitivity reactions in sensitive subjects. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and appropriate medical measures must be initiated. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage, such as cracks, breaks, or structural defects, as this could compromise patient safety and treatment efficacy.

What are the maintenance and reprocessing precautions?

Like all Helmut Zepf brand instruments, this plugger must imperatively be cleaned, disinfected, and sterilized before its first use and after each subsequent use. The manufacturer specifies that it is crucial to visually inspect the product before each use to detect any signs of wear, cracks, or deformation. Due to its design and the materials used, there is no defined maximum limit of processing cycles, but the use of damaged or worn products is prohibited. Compatibility with other cleaning and sterilization products must be verified beforehand to maintain the integrity of the medical stainless steel.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects rigorous quality standards for the production of manual dental instruments. The product is classified as a Class I medical device (Class Ir according to certain reprocessing mentions). It is essential to follow the instructions for use and safety provided by Helmut Zepf to ensure clinical compliance. The manufacturing process in medical stainless steel ensures durability adapted to the requirements of dental practices, provided that the sterilization and maintenance protocols recommended by the manufacturer are strictly applied.


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Specifications

Manufacturer Helmut Zepf
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