DENTAL EXTRACTION FORCEPS. ENGLISH PATTERN. FIGURE 35M. - Helmut Zepf (12.235.08ZTI) - Delynov

What is the Helmut Zepf figure 35M extraction forceps?

The Helmut Zepf figure 35M extraction forceps (reference 12.235.08ZTI) is an English pattern surgical instrument intended for dental avulsion. Manufactured from high-quality medical stainless steel, this instrument is designed to meet the requirements of oral surgery and implantology. Its robust structure and specific configuration allow for optimal handling by the practitioner during extraction maneuvers. As a Class I medical device, it is specifically developed by Helmut Zepf Medizintechnik GmbH to ensure reliable performance during daily clinical interventions in dental practices.

What are the clinical indications?

This device is indicated for tooth extraction within the framework of dental and oral surgeries. Its primary use concerns the avulsion of permanent teeth, specifically as an upper premolar forceps according to the figure 35M configuration. The instrument allows for the application of necessary forces to break ligament fibers and extract the tooth from its socket. It is exclusively reserved for use by qualified healthcare professionals, thus ensuring safe application in compliance with current clinical protocols for simple or complex extractions.

What are the technical characteristics?

The Helmut Zepf 12.235.08ZTI extraction forceps is distinguished by its medical stainless steel construction, a material chosen for its resistance to repeated processing cycles. Its English pattern design (figure 35M) ensures ergonomics adapted to specific access areas in the mouth. The instrument is delivered non-sterile and requires a complete preparation protocol before each use. Due to its metallic composition, it is imperative to check for the absence of visible damage such as cracks or defects on the active parts before any surgical intervention.

What are the contraindications for use?

The main contraindication related to the use of these forceps is the patient's known hypersensitivity or intolerance to metals, particularly the medical stainless steel used for its manufacture. Contact with the instrument in a sensitive patient can trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf Medizintechnik GmbH recommends immediate cessation of the intervention and the implementation of necessary corrective medical measures. It is therefore crucial to evaluate the patient's allergic history before use.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The reprocessing cycle must be complete to ensure the safety of the patient and the practitioner. It is essential to inspect the instrument before each intervention to detect any wear, breakage, or cracks on the cutting edges. The use of damaged products is strictly prohibited. Although no maximum limit for processing cycles is defined by the manufacturer, the physical condition of the steel determines the end of life of the device.

Who is the manufacturer and what standards are respected?

The extraction forceps is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the conformity of its products with safety and performance requirements for manual surgical instruments. Each instrument is identified by a precise technical reference (12.235.08ZTI) allowing for rigorous traceability. Compliance with the cleaning and sterilization instructions issued by Helmut Zepf is essential to maintain the device's conformity during clinical use.

State of the art

Surgical medical consumables play a decisive role in operative safety.