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English pattern dental extraction forceps, figure 79 - Helmut Zepf (12.079.95Z) - Delynov

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The Davier à forme anglaise, figure 79 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.079.95Z.
  • Reserved for healthcare professionals. Read instructions carefully before use.

146.59 € 146.59 EUR 146.59 € Tax Included

146.59 € Tax Included

(146.59 € / Units)
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Instrument

What is the Helmut Zepf figure 79 extracting forceps?

The Helmut Zepf figure 79 extracting forceps is a high-quality manual dental instrument, designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this tool is specifically developed to meet the requirements of dental surgeons during tooth extractions. Its English pattern structure is adapted to the oral anatomy to ensure efficient handling. This device belongs to the category of reusable consumables and benefits from a robust design inherent to the manufacturer's expertise. Its technical reference is code 12.079.95Z, guaranteeing precise identification within the Helmut Zepf range.

What are the clinical indications for these forceps?

This device is indicated as a manual dental instrument for exodontia procedures. More specifically, the figure 79 English pattern forceps are commonly used for the extraction of lower wisdom teeth. Its role is to allow a secure grip of the tooth to facilitate its luxation and removal from the socket. It is intended exclusively for professional use by health practitioners qualified in oral surgery or dentistry. The use of this instrument is part of curative dental care requiring the avulsion of specific dental organs in the mandible.

What are the technical characteristics of the 12.079.95Z forceps?

The Helmut Zepf 12.079.95Z forceps are characterized by their manufacture in medical stainless steel, a material chosen for its resistance and its ability to undergo repeated sterilization cycles. As a manual instrument, it does not contain electronic components or automated mechanisms. Its morphology, known as figure 79, is optimized for access to the posterior areas of the lower jaw. The manufacturer states that due to the product design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, although the instrument must be inspected for any visible damage before each use.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns metal intolerance. Contact with the medical stainless steel instrument may cause a hypersensitivity reaction in certain sensitive patients. If such a reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before any use. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise the safety of the care.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The reprocessing process must be complete to ensure aseptic safety. It is essential to check for the absence of wear or visible damage, such as cracks or defects on the active parts, before each intervention. Never use damaged or worn products. Compatibility with other products used during surgery must also be verified beforehand. Strict compliance with these safety and maintenance instructions is essential to maintain the integrity of the stainless steel instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of these forceps is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. As a manual dental instrument, it meets the quality and safety requirements imposed on medical devices intended for healthcare professionals. The manufacturer emphasizes the importance of systematic cleaning and sterilization to ensure the compliance of the instrument during its clinical use. Traceability is ensured by the reference 12.079.95Z, allowing for precise identification of the model within the catalog of this recognized manufacturer in the dental instrumentation sector.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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