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

What is the Helmut Zepf double periotome (26.182.23OX)?

The P3/P2 Combination periotome from the Helmut Zepf brand is a specialized manual dental instrument. Designed in high-quality medical stainless steel, this tool is a double periotome allowing for efficient handling during oral surgery procedures. Its structure is specifically adapted to meet the requirements of healthcare professionals seeking a reliable instrument for the initial luxation of teeth. This device is delivered non-sterile and requires a complete cleaning and sterilization protocol before each use to ensure the safety of the patient and the practitioner.

What are the clinical indications for this instrument?

The intended use for this Helmut Zepf instrument is that of a classic manual dental instrument. In clinical practice, the double periotome is indicated for the precise sectioning of the periodontal ligament (desmodontium) before a tooth extraction. Its use allows for the disinsertion of the tooth from its socket while minimizing compression of the surrounding bony walls. It is particularly useful in atraumatic extraction protocols, prior to immediate implant placement or for alveolar ridge preservation.

What are the technical characteristics of product 26.182.23OX?

The P3/P2 Combination periotome, referenced under code 26.182.23OX at Delynov, is characterized by its manufacture in medical stainless steel. It is a double-ended instrument, offering two complementary working shapes to adapt to the root anatomy. As a Class I device, it meets the rigorous manufacturing standards of Helmut Zepf Medizintechnik GmbH. Before any use, the practitioner must imperatively inspect the instrument to detect any visible damage, such as cracks, breaks, or defects on the cutting edges, and never use a worn or damaged product.

What are the contraindications for using this periotome?

The main medical contraindication documented by the manufacturer Helmut Zepf concerns metal intolerance. Contact with the medical stainless steel instrument may trigger a hypersensitivity reaction in certain sensitive patients. If such a reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, the use of this instrument is strictly reserved for qualified healthcare professionals proficient in dental surgery techniques.

What are the maintenance and reprocessing precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use, as well as before each subsequent use. The reprocessing process must be complete and rigorous. Due to the design of the instrument and the materials used, there is no defined maximum limit for the number of sterilization cycles; the product's lifespan depends on functional wear and the appearance of visible damage. It is crucial to check compatibility with other products used simultaneously during the surgical procedure.

Who is the manufacturer and what standards are met?

The official manufacturer of this device is the company HELMUT ZEPF Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This periotome is classified as a Class I medical device according to the current regulations. The manufacturer insists on strict compliance with the provided instructions for use and safety. As a Class I product, it is designed to meet the safety and performance requirements for manual dental surgery instruments, ensuring traceability and manufacturing quality in accordance with European standards for medical devices.

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