ENGLISH PATTERN DENTAL EXTRACTION FORCEPS FIGURE 36N - Helmut Zepf dental extraction forceps (12.036.07Z) - Delynov

What is the Helmut Zepf figure 36N forceps?

The English pattern forceps figure 36N, referenced under code 12.036.07Z at Delynov, is a manual instrument specifically developed by Helmut Zepf Medizintechnik GmbH. Designed for dental extraction, this instrument is manufactured from high-quality medical stainless steel to meet the requirements of oral surgery. Its robust structure allows for a grip adapted to avulsion movements. This device is delivered non-sterile and requires a complete preparation protocol before any clinical use in a dental office or hospital environment.

What are the clinical indications for these forceps?

This Helmut Zepf forceps is indicated for manual dental extraction. As an oral surgery instrument, it is used in avulsion protocols to facilitate the removal of teeth from their sockets. Its use is strictly reserved for qualified healthcare professionals. It is particularly used in the preliminary stages of bone reconstruction procedures or implant placement, where the extraction must be performed with instruments complying with medical standards to ensure patient safety.

What are the technical characteristics of this instrument?

The figure 36N forceps (reference 12.036.07Z) is characterized by its medical stainless steel construction, a material chosen for its resistance and compatibility with sterilization cycles. This device belongs to Class I according to the regulatory classification of medical devices. Helmut Zepf Medizintechnik GmbH specifies that, due to the design and materials used, there is no defined maximum limit for the feasible processing cycles, although the instrument must be inspected for any visible damage before each use.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or metal intolerance. Contact with medical stainless steel can trigger a reaction in sensitive patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before using this manual instrument.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. The reprocessing process must be complete to ensure asepsis. Before each use, the practitioner must visually inspect the instrument to detect any potential damage or signs of wear such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to maintain operative safety.

Who is the manufacturer and what standards are respected?

The official manufacturer is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This forceps is a Class I medical device, complying with the regulatory requirements applicable to manual dental instruments. The manufacturer emphasizes that its products are intended exclusively for healthcare professionals. Compliance with cleaning and sterilization protocols, as well as verifying compatibility with other products used during the intervention, are essential steps defined by the manufacturer to ensure the proper functioning of the device.

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