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Tunneling kit - Helmut Zepf (46.040.00) - Delynov

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The Kit pour tunnelisation - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 46.040.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

314.03 € 314.03 EUR 314.03 € Tax Included 615.49 €

314.03 € Tax Included 615.49 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf Tunneling Kit?

The Helmut Zepf Tunneling Kit (reference 46.040.00) is a set of manual instruments specifically selected for periodontal micro-surgery procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, this kit consists of instruments made of high-quality medical stainless steel. It is designed to allow practitioners to perform tunneling techniques, a minimally invasive approach aimed at treating gingival recessions. As a Class I device, it meets the safety requirements for reusable dental instruments, requiring a complete cycle of cleaning, disinfection, and sterilization before each clinical use.

What are the clinical indications for this kit?

This periodontal tunneling kit is indicated for performing coronally or laterally positioned flaps without relieving incisions. It is primarily used in periodontal plastic surgery for the treatment of marginal tissue recessions. The instruments allow for the preparation of the recipient bed by delicately detaching the gingiva from the periosteum or by dissecting within the connective tissue. This approach preserves collateral vascularization and the integrity of the interdental papillae, thus optimizing aesthetic and functional results during the placement of connective tissue grafts or tissue substitutes.

What are the technical characteristics of the instruments?

The instruments included in this kit (code 46.040.00) are manufactured from medical stainless steel, a material chosen for its mechanical strength and its ability to undergo repeated sterilization cycles. The design of each instrument is optimized for navigation in the restricted spaces characteristic of the tunnel technique. The manufacturer, Helmut Zepf, specifies that the condition of the instruments must be checked before each use to detect any visible damage such as cracks, breaks, or defects on the cutting edges. The absence of a defined maximum limit for processing cycles depends on rigorous maintenance and the wear observed by the healthcare professional.

What are the contraindications for the use of these instruments?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns patients with a known intolerance or hypersensitivity to metals. Contact with medical stainless steel can trigger a hypersensitivity reaction in these individuals. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of instruments showing signs of wear, corrosion, or structural damage is strictly prohibited to ensure patient safety and the effectiveness of the surgical procedure.

What are the maintenance and sterilization precautions?

Helmut Zepf tunneling instruments are delivered non-sterile and must undergo a complete reprocessing protocol before the first use and after each subsequent use. This process includes thorough cleaning, disinfection, and sterilization. It is crucial to clean each product individually to remove all biological residue. The practitioner must carefully inspect the devices to identify any premature wear or cracks. Due to their design and the materials used, there is no predefined maximum number of sterilization cycles, the end of the product's life being determined by the appearance of physical defects or a loss of functionality.

Who is the manufacturer and what standards are respected?

The kit is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer insists that the use of these instruments is strictly reserved for qualified healthcare professionals. Compliance with safety and performance requirements is ensured by adherence to the rigorous manufacturing protocols of Helmut Zepf. Users must ensure compatibility with other products used simultaneously and scrupulously follow the instructions for use and safety provided to maintain the integrity of the device.


State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.

Specifications

Manufacturer Helmut Zepf
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