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Root Canal Spreader Foular Luks - Helmut Zepf (19.512.13) - Delynov

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The Fouloir de Canal Radiculaire Luks - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.512.13.
  • Reserved for healthcare professionals. Read instructions carefully before use.

41.37 € 41.37 EUR 41.37 € Tax Included

41.37 € Tax Included

(41.37 € / Units)
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Instrument

What is the Helmut Zepf Luks root canal plugger?

The Luks root canal plugger, referenced under code 19.512.13, is a specialized manual instrument developed by Helmut Zepf Medizintechnik GmbH. Designed for endodontic instrumentation, this tool is manufactured from high-quality medical stainless steel to ensure optimal resistance during clinical procedures. Its structure is specifically adapted for handling canal filling materials. This device belongs to the category of reusable consumables, requiring a strict reprocessing protocol between each patient. As a precision instrument, it allows the practitioner to exert controlled pressure during the final phase of endodontic treatment.

What are the clinical indications for this instrument?

The Luks plugger is indicated for root canal treatment procedures, specifically for the condensation of gutta-percha or other root filling materials. Its role is to ensure apical and lateral sealing by compacting the filling material homogeneously against the canal walls. This instrument is used by dental surgeons and endodontic specialists during the obturation phase, after the shaping and disinfection of the canal system. Its use is strictly reserved for qualified healthcare professionals operating within the framework of conservative dental care or endodontic surgeries.

What are the technical characteristics of the 19.512.13 plugger?

The Helmut Zepf plugger (ref. 19.512.13) is characterized by its medical stainless steel construction, a material chosen for its biocompatibility and mechanical resistance. It is a manual instrument delivered non-sterile, which implies a mandatory cleaning, disinfection, and sterilization step before the first use and after each subsequent use. Its design allows for efficient transmission of the axial force required for thermal or cold condensation. Due to its metallic nature, constant visual verification is required to detect potential damage such as cracks or defects on the active parts before any intervention.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Contact with the medical stainless steel instrument can trigger an allergic reaction in certain sensitive patients. If such a hypersensitivity reaction occurs during the procedure, the intervention must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of this instrument is prohibited if it shows visible signs of wear, cracks, or breaks, as this could compromise patient safety or the effectiveness of the endodontic treatment.

What are the maintenance and sterilization precautions?

As Helmut Zepf Medizintechnik GmbH products are delivered non-sterile, they must imperatively undergo a complete cleaning, disinfection, and sterilization cycle before use. It is crucial to clean each instrument individually to remove any residue before autoclaving. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit for processing cycles, as long as the instrument does not show visible damage or defects on the edges. Compatibility with other cleaning products must also be verified beforehand by the dental practice.

Who is the manufacturer and what standards are respected?

This plugger is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. The device is classified as a Class I instrument according to current regulations (Classe Ir - MDC0483). The manufacturer insists on strict compliance with safety and usage instructions to maintain clinical safety and conformity. As a Class I medical device, it meets the quality requirements for manual instruments intended for dental surgery. Each product must be inspected by the healthcare professional to ensure the absence of cracks or ruptures before its integration into the care workflow.


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Manufacturer Helmut Zepf
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