ANGLO-SAXON DENTAL EXTRACTION FORCEPS FIGURE 36N - Helmut Zepf Dental Extraction Pliers (12.236.07ZTI) - Delynov

What is the Helmut Zepf extraction forceps English pattern Figure 36N?

The extraction forceps English pattern Figure 36N, referenced under code 12.236.07ZTI by the manufacturer Helmut Zepf Medizintechnik GmbH, is a manual surgical instrument in the ROG category. Manufactured from high-quality medical stainless steel, this device is designed to withstand mechanical stress during exodontia procedures. Its specific structure, known as 'English pattern', is adapted to the dental anatomy to allow a firm and secure grip. This equipment is delivered non-sterile and must undergo a complete cleaning, disinfection, and sterilization protocol before its first use and after each clinical act.

What are the clinical indications for these premolar extraction forceps?

The intended purpose defined by the manufacturer Helmut Zepf for this instrument is the extraction of teeth. Specifically, the configuration of this 36n forceps is primarily intended for the avulsion of premolars at the level of the mandibular arch. In oral and implant surgery, it is used during alveoloplasty phases or site preparation before implant placement, when extraction of the dental element is required. Its use is strictly reserved for qualified healthcare professionals mastering dental surgical techniques. The instrument must be inspected before each use to detect any visible damage such as cracks or defects on the active parts.

What are the technical characteristics of the 12.236.07ZTI forceps?

This medical device, identified by reference 12.236.07ZTI, belongs to Class I according to current regulations. It is entirely designed in medical stainless steel, a material chosen for its biocompatibility and resistance to corrosion provided proper maintenance is performed. Its ergonomic design allows for efficient force transmission while minimizing the risk of slipping. Due to the nature of the materials and the robust design of the product, Helmut Zepf indicates that there is no maximum limit defined for the number of processing cycles (cleaning and sterilization), the lifespan depending on actual wear and the absence of visible damage.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer concerns the patient's known hypersensitivity to metallic components. Contact with medical stainless steel can trigger an intolerance or hypersensitivity reaction in certain subjects. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and the necessary medical measures must be taken. Furthermore, it is strictly forbidden to use the instrument if it shows signs of wear, breakage, or cracks on the cutting edges, as this could compromise patient safety and the effectiveness of the surgical act.

What are the maintenance and sterilization precautions?

As it is a non-resorbable and reusable instrument, the Helmut Zepf forceps require rigorous reprocessing. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to check the cleanliness of each product and ensure the absence of organic residues before autoclaving. The manufacturer emphasizes the importance of checking compatibility with other cleaning and disinfection products used. Inadequate maintenance can alter the properties of the stainless steel and reduce the longevity of the instrument or compromise the asepsis of the surgical field.

Who is the manufacturer and what standards are respected?

The forceps are manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I. The manufacturer ensures the compliance of its products with the regulatory requirements relating to medical devices (MDR). Healthcare professionals must refer to the instructions provided by Helmut Zepf to guarantee use in accordance with the intended indications. The traceability and manufacturing quality of this instrument meet the high standards required for dental surgical instrumentation in Europe, thus guaranteeing optimal safety during extraction procedures.

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