P3 Periotome - Helmut Zepf (26.182.13) - Delynov

What is the Helmut Zepf P3 Periotome?

The P3 Periotome, bearing reference 26.182.13, is a specialized manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from medical stainless steel, a standard material for surgical instrumentation ensuring resistance adapted to the constraints of oral surgery. Its structure is specifically designed to be inserted into the periodontal space. As a dental periotome, it allows the practitioner to perform precise movements during the initial phases of avulsion. This device belongs to Class I of medical devices, meeting the regulatory requirements for non-invasive or invasive instruments for temporary use.

What are the clinical indications for the dental periotome?

The main indication for this Helmut Zepf manual instrument is the sectioning of the periodontal ligament. In clinical practice, it is used during extraction surgeries to break the ligament attachments circumferentially around the root. This step is crucial to facilitate extraction without applying excessive leverage forces that could damage the alveolar bone. Its use is particularly recommended in immediate implant placement protocols, where preserving the integrity of the buccal bone plate is decisive for the future aesthetic and functional success of the implant treatment.

What are the technical characteristics of model 26.182.13?

Model 26.182.13 is characterized by an ergonomic design specific to Helmut Zepf standards, using medical grade stainless steel. This instrument is delivered non-sterile by the manufacturer, which requires a rigorous processing protocol before any use. Technical features include a sharpened working part allowing precise penetration into the periodontal ligament. Before each intervention, the practitioner must imperatively check for the absence of visible damage, such as cracks or defects on the cutting edges. The integrity of the instrument is essential to guarantee the effectiveness of the ligament sectioning and patient safety during the operative act.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known patient hypersensitivity to metals. As the instrument is composed of medical stainless steel, contact may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to evaluate the patient's allergic history before using this dental periotome. Furthermore, the use of the instrument is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the maintenance and reprocessing precautions?

As the P3 Periotome is a non-sterile instrument upon delivery, it must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. The manufacturer specifies that due to the design of the instrument and the materials used, there is no defined maximum limit of processing cycles, as long as the instrument does not show wear or damage. A careful visual inspection is required to detect any breakage or loss of sharpness on the cutting edges. The use of a damaged instrument is prohibited to avoid any risk of intraoperative complication or cross-contamination.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This periotome is classified as a Class I device according to current regulations. Compliance with manufacturing protocols ensures the conformity of the medical stainless steel used for this manual instrument. As a Helmut Zepf product, it benefits from the brand's expertise in the field of high-precision dental instrumentation. The manufacturer emphasizes that compatibility with other products used during surgery must be verified beforehand by the healthcare professional to ensure the overall safety of the treatment.

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