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English pattern dental extraction forceps, figure 51-A - Helmut Zepf (12.051.01Z) - Delynov

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The Davier à forme anglaise, figure 51-A - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.051.01Z.
  • Reserved for healthcare professionals. Read instructions carefully before use.

100.23 € 100.23 EUR 100.23 € Tax Included 133.48 €

100.23 € Tax Included 133.48 €

(100.23 € / Units)
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Instrument

What is the Helmut Zepf 12.051.01Z English pattern forceps?

The English pattern forceps, figure 51-A, referenced under code 12.051.01Z, is a manual instrument developed by Helmut Zepf Medizintechnik GmbH. It belongs to the category of surgical consumables and is manufactured from high-quality medical stainless steel. This device is specifically designed for oral surgery interventions requiring robust and reliable instrumentation. As a Class I device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use. Its structure is adapted to the mechanical stresses encountered during dental avulsions, offering a grip consistent with traditional English pattern standards for healthcare professionals.

What are the clinical indications for these root forceps?

These root forceps are indicated for dental extraction procedures, specifically for the removal of roots. Its use is reserved for qualified healthcare professionals in dental and oral surgery. The instrument allows for firmly grasping radicular structures to facilitate their luxation and removal from the socket. The manufacturer Helmut Zepf specifies that this manual instrument is intended for precise clinical use where direct manipulation of hard tissues is necessary. It is integrated into the standard protocol for simple or complex extraction, ensuring adequate force transmission for the avulsion of remaining fragments.

What are the technical characteristics of this device?

The Helmut Zepf 12.051.01Z forceps are characterized by their medical stainless steel construction, a material chosen for its corrosion resistance and its ability to undergo repeated sterilization cycles. Being a Class I instrument, it is delivered non-sterile and must undergo complete processing before its first use. Its morphology corresponds to figure 51-A of the English pattern nomenclature, optimized for access to radicular areas. It does not have a defined maximum limit of processing cycles, as this depends on the eventual appearance of visible damage or wear on the instrument during clinical 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. If a patient has a known sensitivity or allergy to medical stainless steel components, the use of this instrument may trigger a hypersensitivity reaction. In the event that 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 check the patient's allergic history before any contact with surgical instrumentation to prevent any undesirable side effects related to the materials.

What are the maintenance and safety precautions?

All instruments must be rigorously cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to perform a complete cleaning to remove all residue before the sterilization cycle. Before each intervention, the practitioner must visually inspect the forceps to detect any damage or wear, such as cracks, breaks, or defects on the active parts. The use of damaged or worn products is strictly prohibited. Compatibility with other products used during the surgical act must also be verified beforehand to ensure patient safety and the effectiveness of the operative procedure.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. These forceps are classified as a Class I medical device according to current regulations. The manufacturer emphasizes that these products are exclusively reserved for healthcare professionals. The reprocessing process is possible thanks to the design and materials used, although no cycle limit is predefined. Compliance with cleaning and sterilization protocols is the responsibility of the practitioner, in accordance with the instructions provided by Helmut Zepf to maintain the integrity of the surgical instrumentation.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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