Periotome P3/P2 Combination - Helmut Zepf (26.182.23) - Delynov

What is the Helmut Zepf P3/P2 periotome?

The P3/P2 periotome, referenced under code 26.182.23, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in high-quality medical stainless steel, this double periotome is specifically structured for interventions requiring a delicate approach to periodontal tissues. Its composition guarantees resistance adapted to the constraints of oral surgery while maintaining the thinness necessary to insert into the periodontal space. As a Class I device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use.

What are the clinical indications for the double periotome?

This instrument is indicated for gentle extraction, a technique aimed at minimizing trauma to the surrounding alveolar bone. Clinically, it is used to section the periodontal ligament (desmodontium) around the entire circumference of the root. This step is crucial before the actual avulsion, particularly in immediate loading protocols or alveolar ridge preservation where the integrity of the bone walls is paramount. The use of this Helmut Zepf double periotome allows the practitioner to access different root surfaces with a single instrument.

What are the technical characteristics of model 26.182.23?

The Helmut Zepf 26.182.23 periotome is distinguished by its double-ended configuration, combining P3 and P2 profiles. Made of medical stainless steel, it features sharpened cutting edges designed to penetrate the narrow periodontal space. The manufacturer emphasizes the importance of checking for visible damage, such as cracks, breaks, or defects on the cutting edges before each use. Being delivered non-sterile, this instrument requires a full cycle of cleaning, disinfection, and sterilization before its first use and between each patient.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns patients with a known intolerance or hypersensitivity to metals, as the instrument is composed of medical stainless steel. A hypersensitivity reaction may be triggered upon contact. If such a reaction occurs during the intervention, the procedure must be immediately stopped and appropriate medical measures must be taken. Furthermore, the use of an instrument showing visible signs of wear or structural defects is strictly prohibited to guarantee patient safety.

What are the maintenance and reprocessing precautions?

Like any reusable stainless steel instrument, this periotome must undergo a strict reprocessing protocol. Before the first use and after each procedure, it must be cleaned, disinfected, and sterilized. Due to its design and the materials used, the manufacturer Helmut Zepf does not establish a defined maximum limit of treatment cycles but insists on systematic visual inspection. Any blunt, bent instrument or one showing micro-cracks must be removed from service. Compliance with these safety instructions ensures the longevity of the tool and aseptic safety in the practice.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This periotome is classified as a Class I medical device according to current regulations. The manufacturer guarantees the traceability and compliance of its products intended exclusively for healthcare professionals. Each instrument is designed to meet the requirements of modern dental surgery, combining the rigor of German manufacturing with the clinical needs of gentle extraction. Cleaning and sterilization procedures must follow current hospital standards for reusable invasive devices.

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