EXTRACTING FORCEPS. ENGLISH PATTERN FIG 36M - Helmut Zepf (12.236.08ZTI) - Delynov

What is the Helmut Zepf FIG 36M extraction forceps?

The Helmut Zepf extraction forceps (reference 12.236.08ZTI) is a Class I manual instrument intended for dental extraction. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device adopts a specific English pattern (figure 36M). Its structure is designed to withstand the mechanical stresses associated with avulsion while ensuring optimal durability. As an oral surgery instrument, it comes in a form similar to dental pliers, allowing the practitioner to apply the necessary forces to remove the tooth from its socket. This product is delivered non-sterile and requires a complete preparation protocol before any intervention.

What are the clinical indications for these molar dental forceps?

This dental surgery forceps is exclusively indicated for the extraction of teeth. Its use is reserved for qualified healthcare professionals working in dental surgery, stomatology, or implantology. The instrument is used to securely grasp the tooth in order to proceed with its luxation and final extraction. Although the figure 36M is often associated with specific segments of the arch, its intended purpose remains general dental avulsion according to the clinical needs identified by the practitioner. The use of this instrument must be preceded by a thorough examination of the condition of the tooth and surrounding tissues to ensure an appropriate procedure.

What are the technical characteristics of this instrument?

The Helmut Zepf 12.236.08ZTI forceps is characterized by its medical stainless steel construction, a material chosen for its corrosion resistance and its ability to undergo repeated sterilization cycles. This English pattern model meets the design standards of the Helmut Zepf brand, ensuring efficient transmission of manual force. The manufacturer states that, due to the product design and materials used, there is no defined maximum limit for the number of processing cycles achievable, although the instrument must be visually inspected before each use to detect potential damage such as cracks, breaks, or defects on the active parts.

What are the contraindications for the use of this device?

The main medical contraindication lies in the patient's known hypersensitivity or intolerance to metals, particularly components of medical stainless steel. Contact with the instrument can trigger a hypersensitivity reaction in sensitive subjects. The manufacturer Helmut Zepf Medizintechnik GmbH stipulates that if such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to assess the patient's allergic history before using this surgical instrument.

What are the maintenance and sterilization precautions?

Like any reusable Class I instrument, this forceps must be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The reprocessing process must be complete to ensure the safety of the patient and the practitioner. Before each use, it is very important to check for the absence of visible damage, such as cracks or excessive wear of the cutting edges. A damaged or worn product should never be used. As Helmut Zepf products are delivered non-sterile, strict compliance with the sterilization protocols in force in dental practices or hospital environments is mandatory to maintain the integrity of the device.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This forceps is classified as a Class I medical device according to current regulations. The manufacturer ensures the compliance of its products with safety and performance requirements for the intended use in dental surgery. Traceability is ensured by the technical reference 12.236.08ZTI. As a reusable instrument, its design allows for frequent reprocessing without a predefined limit of cycles, subject to the maintenance of its structural and functional integrity verified by the healthcare professional.

State of the art

Surgical medical consumables play a decisive role in operative safety.