Periotome P2 - Helmut Zepf (26.182.12) - Delynov - Dental Surgery Instrument

What is the periotome P2 - Helmut Zepf?

The periotome P2 is a manual surgical instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device, identified under the reference 26.182.12, is manufactured from high-quality medical stainless steel. It belongs to the category of reusable consumables after a complete reprocessing cycle. Its structure is specifically designed to be inserted into the periodontal space. As a precision instrument, it allows the practitioner to access narrow areas between the tooth root and the alveolar bone. This product is delivered non-sterile and requires rigorous preparation before its first use in a dental surgery office or hospital environment.

What are the clinical indications for the periotome?

In oral surgery and implantology, the periotome is indicated for deep syndesmotomy. Its primary role is to section the periodontal ligaments (alveolo-dental ligament) in order to disconnect the tooth from its bony socket without exerting excessive lateral pressure. This technique is particularly recommended during extractions for immediate implantation, where the conservation of the alveolar bone and the crest is critical. The use of the periotome p2 helps limit trauma to the surrounding soft tissues and maintain the gingival architecture. It is an indispensable tool for so-called atraumatic extractions performed by dental surgeons and stomatologists.

What are the technical characteristics of model 26.182.12?

The surgical periotome referenced 26.182.12 is distinguished by its medical stainless steel design, ensuring the necessary resistance to mechanical stress during initial luxation. Although specific dimensions are not listed, the Helmut Zepf range is recognized for the fineness of its working parts, allowing for precise insertion into the sulcus. This device is classified as a Class I instrument according to medical device regulations. It is designed to withstand repeated cycles of cleaning, disinfection, and steam sterilization without alteration of its physical properties, subject to compliance with the reprocessing protocols defined by the manufacturer Helmut Zepf Medizintechnik GmbH.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a reaction occurs during the surgical procedure, the procedure must be immediately interrupted and the necessary clinical measures must be taken. Furthermore, use is strictly reserved for qualified healthcare professionals. The use of an instrument showing visible damage, such as cracks, breaks, or defects on the cutting edges, is formally prohibited to avoid any risk of intraoperative complication.

What are the maintenance and reprocessing precautions?

The periotome p2 is delivered non-sterile. Before the first use and after each intervention, the instrument must undergo a complete cycle of cleaning, disinfection, and sterilization. The manufacturer specifies that due to the robust design and materials used, there is no defined maximum limit for the number of treatment cycles, as long as functional integrity is preserved. It is imperative to inspect the tool before each use to detect any wear or corrosion. Cleaning must be meticulous to remove all organic residues. Compatibility with other cleaning and disinfection products must be verified beforehand to ensure the longevity of this stainless steel instrument.

Who is the manufacturer and what standards are respected?

This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. The product complies with Class I medical device regulations (Class Ir according to certain reprocessing nomenclatures). Helmut Zepf is a recognized manufacturer in the dental instrumentation sector for its adherence to rigorous manufacturing standards. Following the instructions for use and safety provided by Helmut Zepf Medizintechnik GmbH is essential to ensure the safety of the patient and the practitioner. The device is intended exclusively for professional use by dental surgery experts trained in minimally invasive extraction techniques.

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Surgical medical consumables play a decisive role in operative safety.