Periotome insert P 4, mesial / distal angled - Helmut Zepf (26.182.04) - Delynov

What is the Helmut Zepf P 4 periotome insert?

The P 4 periotome insert, referenced under code 26.182.04, is a precision instrument developed by Helmut Zepf Medizintechnik GmbH. It is an interchangeable periotome blade designed to be mounted on a suitable handle. Its structure is distinguished by a double mesial and distal angulation, allowing the practitioner to reach ligamentous areas that are difficult to access with classic straight instrumentation. This device is manufactured according to the quality standards of the Helmut Zepf brand, guaranteeing a blade thinness essential for insertion into the periodontal space without damaging the surrounding bone structures.

What are the clinical indications for this instrument?

This periotome insert is primarily indicated in oral surgery and implantology during tooth extractions, particularly those aimed at maximum alveolar preservation. Its use allows for the breaking of the ligament attachment around the entire circumference of the root, especially on the mesial and distal aspects thanks to its specific shape. By releasing the tooth from its periodontal attachments before using forceps or elevators, this instrument limits the mechanical stress exerted on the alveolar bone, which is crucial for the subsequent placement of implants or for maintaining gingival aesthetics.

What are the technical characteristics of reference 26.182.04?

Reference 26.182.04 corresponds to the P 4 model of the Helmut Zepf range. Its major technical characteristic lies in its specific angulation, optimized for work in mesial and distal zones. As an interchangeable periotome blade, it offers flexibility in instrumentation management in the practice, allowing only the active tip to be replaced. The thinness of its working part is calibrated to penetrate the sulcus and descend along the root. The design by Helmut Zepf Medizintechnik GmbH ensures efficient transmission of manual force for a clean sectioning of the ligament fibers.

What are the contraindications for the use of this insert?

Contraindications for the use of this insert are related to clinical extraction protocols and the patient's health status. It must not be used if the practitioner does not have the compatible handle guaranteeing secure fixation of the insert. Clinically, its use may be proscribed in cases of severe dental ankylosis where the periodontal space is non-existent, making the insertion of the periotome blade impossible or risky for the integrity of the instrument. As with any invasive device, a complete anamnesis is required to rule out risks related to uncontrolled systemic pathologies or healing disorders.

What are the maintenance and durability precautions?

Although specific resorption data do not apply to this non-resorbable metallic instrument, its durability depends on compliance with the sterilization and cleaning cycles recommended by Helmut Zepf. It is imperative to check the integrity of the tip and the angulation before each intervention. A blunt or bent blade loses its effectiveness and can increase the risk of tissue trauma. The insert must be correctly cleaned to remove any organic residue in the assembly areas with the handle before undergoing a standard autoclave cycle, in accordance with current hygiene protocols in dental surgery.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the manufacture of high-precision surgical instruments. Production follows rigorous processes to guarantee the reliability of instruments intended for oral surgery. Although specific details of the CE marking or regulatory class are not explicitly stated in the source documentation, Helmut Zepf products are designed to meet the professional requirements of dental surgeons and implantologists. It is recommended to consult the instructions for use attached to the product or contact the manufacturer to obtain certificates of conformity and specific reprocessing instructions.

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