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EXTRACTING FORCEPS. ENGLISH PATTERN. FIG.17 - Helmut Zepf (12.217.00ZTI)

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The DAVIER. FORME ANGLAISE. FIG.17 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.217.00ZTI.
  • Reserved for healthcare professionals. Read instructions carefully before use.

224.94 € 224.94 EUR 224.94 € Tax Included 376.31 €

224.94 € Tax Included 376.31 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf Fig.17 forceps?

The Helmut Zepf forceps (reference 12.217.00ZTI) is an English pattern surgical instrument specifically designed for dental extraction. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is crafted from high-quality medical stainless steel to ensure optimal resistance during luxation and avulsion maneuvers. As an instrument in the CONSO category, it is classified as a Class I medical device. Its plier-like structure allows for controlled force transmission, meeting the requirements of oral surgery practitioners for handling dental structures during extraction phases.

What are the clinical indications for this forceps?

This forceps is indicated for dental extraction procedures in dental practices or hospital environments. According to the specifications of the manufacturer Helmut Zepf Medizintechnik GmbH, its intended purpose is to serve as an instrument for extracting teeth. Although the Fig.17 nomenclature is traditionally associated with use on molars, the primary indication remains dental avulsion. It is used by healthcare professionals to grasp the dental crown and perform the rotation or tipping movements necessary to break the periodontal ligament before the final removal of the tooth from its socket.

What are the technical characteristics of the 12.217.00ZTI forceps?

The Helmut Zepf Fig.17 forceps is characterized by its manufacture in medical stainless steel, a material chosen for its mechanical properties and compatibility with reprocessing cycles. This Class I medical device is delivered non-sterile and requires rigorous preparation before any use. The English pattern design offers specific ergonomics for access to posterior areas. The manufacturer specifies that due to the quality of the materials used, there is no defined maximum limit for treatment cycles, although the instrument must be inspected for any visible damage or wear before each use.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity to metals. Contact with the medical stainless steel instrument can trigger an intolerance reaction in some patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken accordingly. It is therefore imperative to check the patient's allergic history before use. Furthermore, the use of the instrument is strictly reserved for qualified healthcare professionals mastering extraction techniques.

What are the maintenance and sterilization precautions?

The forceps must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The manufacturer emphasizes the importance of cleaning each product to remove any residue before the sterilization cycle. Before each intervention, the practitioner must inspect the instrument to detect visible damage or wear, such as cracks, breaks, or defects on the cutting edges. It is formally forbidden to use damaged or worn products. As the devices are delivered non-sterile, compliance with reprocessing protocols is crucial to guarantee patient safety and the longevity of the stainless steel.

Who is the manufacturer and what standards are respected?

The official manufacturer of this forceps is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its products with medical requirements for reusable surgical instruments. The manufacturing process is based on the use of medical stainless steel selected for its durability and its ability to undergo repeated cleaning and sterilization cycles. Each instrument is identified by a precise technical reference (12.217.00ZTI) allowing for the traceability of the device within the dental practice.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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