Right-angled syndesmotome for lingual or buccal luxation - Helmut Zepf (17.008.09TI) - Delynov

What is the Helmut Zepf right-angled syndesmotome?

The Helmut Zepf right-angled syndesmotome, referenced under code 17.008.09TI at Delynov, is a precision manual instrument used in oral surgery. Its structure consists of an ergonomic handle and a thin, beveled working part, specifically oriented for interventions in lateral sectors. This tool is designed by Helmut Zepf Medizintechnik GmbH, a manufacturer recognized for the quality of its surgical instrumentation. Unlike straight models, its specific curvature allows for an angled approach, facilitating passage into the gingival-dental sulcus to release ligament attachments without unnecessarily damaging surrounding soft tissues.

What are the clinical indications for this luxator?

The use of this angled syndesmotome is indicated during the initial phases of tooth extraction, particularly for lingual or buccal luxation. In implant and oral surgery, it is used to section the ligament fibers of the periodontium before the application of traction force. Its profile is ideal for practitioners seeking a dental luxation instrument capable of operating in restricted spaces where a straight instrument would be ineffective. It allows for the detachment of the marginal gingiva and the creation of an initial fulcrum point, thus limiting the risk of alveolar ridge fracture during avulsion, a crucial point for preserving pre-implant bone capital.

What are the technical characteristics of the 17.008.09TI instrument?

The Helmut Zepf syndesmotome (reference 17.008.09TI) is distinguished by its active tip angled to the right. This geometric orientation is optimized to follow the anatomy of the dental arches during lingual or buccal luxation maneuvers. The thinness of its tip allows for precise insertion into the periodontal space. Although the exact material specifications are not detailed in the source data, Helmut Zepf instrumentation is traditionally designed to meet sterilization and durability requirements in clinical settings. Its monobloc or assembled design ensures direct transmission of the force exerted by the dental surgeon, guaranteeing optimal tactile feedback when sectioning periodontal fibers.

What are the contraindications for the use of this instrument?

Contraindications for the use of the Helmut Zepf angled syndesmotome are mainly related to the patient's general clinical conditions, such as severe coagulation disorders or local bone pathologies prohibiting any invasive surgery. Technically, the use of this instrument is contraindicated if the root morphology or the position of the tooth does not allow for secure insertion of the blade, at the risk of damaging adjacent anatomical structures such as the alveolar nerve or the maxillary sinus. This instrument should not be used as a lever with excessive force, as its primary function is syndesmotomy and light luxation rather than massive elevation.

What are the maintenance precautions for this non-resorbable device?

As a reusable surgical instrument, this Helmut Zepf syndesmotome must follow a strict protocol of decontamination, cleaning, and sterilization after each use. Although resorption data do not apply here, the durability of the instrument depends on compliance with autoclave cycles and the use of non-corrosive cleaning solutions. The practitioner must regularly inspect the condition of the beveled tip to ensure its sharpness and the absence of micro-cracks. Rigorous maintenance ensures not only patient safety against the risks of cross-contamination but also preserves the mechanical properties of the steel necessary for precise and effective dental luxation.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a German company specializing in high-tech dental instrumentation. Regarding specific certifications, the regulatory class and CE marking are not explicitly mentioned in the current source documentation. However, as a medical device manufacturer operating in the European market, Helmut Zepf subjects its products to current quality controls. It is imperative for the user to refer to the instructions for use and the labels present on the original packaging delivered by Delynov to verify compliance information, recommended sterilization protocols, and any regulatory updates related to the MDR.

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