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Dental Surgical Extracting Pliers Helmut Zepf (14.217.00)

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The DAVIER FORME AMOVIBLE FIGURE 217 - Pince à extraction dentaire Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 14.217.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

100.31 € 100.31 EUR 100.31 € Tax Included

100.31 € Tax Included

(100.31 € / Units)
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Instrument

What is the Helmut Zepf figure 217 forceps?

The figure 217 forceps, referenced under code 14.217.00, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. It is a dental extraction forceps designed specifically for procedures on the lower jaw. Its structure is made of medical stainless steel, a material chosen for its resistance and compatibility with hospital decontamination processes. This model is distinguished by its removable shape adapted to the mandibular anatomy, allowing the dental surgeon to perform avulsions with an optimized grip.

What are the clinical indications for this dental extraction forceps?

This device is indicated for the extraction of teeth and roots located in the mandible. In oral surgery and implantology, the figure 217 forceps is used for simple or complex exodontia prior to the eventual placement of bone substitutes within the framework of GBR (Guided Bone Regeneration). Its use is strictly reserved for qualified healthcare professionals. It allows the mobilization and removal of the dental element from its socket by applying the necessary forces while respecting the integrity of the surrounding tissues, in accordance with current clinical protocols.

What are the technical characteristics of the 14.217.00 forceps?

The Helmut Zepf 14.217.00 forceps is a Class I instrument manufactured from high-quality medical stainless steel. Its technical design is based on ergonomics specific to figure 217, optimized for access to mandibular areas. It is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use, as well as between each patient. The manufacturer does not define a maximum limit of processing cycles, as the lifespan of the instrument depends on maintenance and the absence of visible damage such as cracks or defects on the edges.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Contact with medical stainless steel can trigger a reaction in allergic patients. If such a hypersensitivity reaction occurs during the procedure, the procedure must be immediately stopped and necessary medical measures must be taken. Additionally, the use of the instrument is contraindicated if it shows visible damage, breaks, cracks, or marked wear on the active parts, as this could compromise the safety of the surgical procedure.

What are the maintenance and sterilization precautions?

Like any reusable surgical instrument, this dental extraction forceps requires rigorous maintenance. Before each use, it is imperative to check for the absence of damage and wear. The reprocessing process must include complete cleaning, disinfection, and sterilization. The manufacturer emphasizes that it is crucial to clean each product before use. Due to the quality of the materials used, there is no predefined limit for sterilization cycles, but compatibility with other cleaning and disinfection products must be verified beforehand by the practitioner to guarantee the longevity of the steel.

Who is the manufacturer and what standards are respected?

This forceps 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 complies with strict production standards to guarantee the safety and efficacy of its manual instruments. Healthcare professionals can refer to the manufacturer's instructions for reprocessing and compliant use. As a Class I product, it meets the essential safety requirements, ensuring that the stainless steel used is suitable for prolonged medical use after sterilization.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Helmut Zepf
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