Syndesmotome XTool - Cutting instrument for syndesmotomy - Helmut Zepf (17.008.05TI) - Delynov

What is the Helmut Zepf XTool syndesmotome?

The XTool syndesmotome, reference 17.008.05TI, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is specifically developed for oral surgery procedures requiring a clean separation of ligament tissues. As a dental cutting instrument, its structure is adapted for rigorous handling by healthcare professionals. This device belongs to the category of manual diagnostic and intervention instruments, ensuring a response adapted to the requirements of dental practices and implant surgery centers.

What are the clinical indications for this instrument?

This instrument is indicated for lifting teeth or residual dental roots during the extraction procedure. The cutting syndesmotome allows the practitioner to intervene with precision on the socket to facilitate the removal of the dental element. Its use is strictly reserved for qualified healthcare professionals. It is particularly useful in complex cases where roots are fractured or deeply anchored, requiring a controlled leverage action to minimize damage to surrounding structures during syndesmotomy.

What are the technical characteristics of the 17.008.05TI model?

The Helmut Zepf XTool 17.008.05TI model is distinguished by its medical-grade stainless steel composition, ensuring the necessary resistance to mechanical stress during elevation. Although the syndesmotome price may vary by distributor, its technical specifications meet the manufacturing standards of Helmut Zepf Medizintechnik GmbH. The instrument features cutting edges that must undergo constant verification to detect any wear, cracks, or defects before each use, thus guaranteeing its operational efficiency.

What are the contraindications for the use of this device?

The main contraindication lies in the patient's known hypersensitivity to metals. Contact with medical stainless steel can trigger an intolerance reaction or a hypersensitivity reaction in certain subjects. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf recommends immediate cessation of the intervention and the implementation of necessary medical measures. It is therefore imperative to validate the absence of metal allergies before any clinical handling.

What are the maintenance and sterilization precautions?

Helmut Zepf instruments are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The manufacturer emphasizes the critical importance of visual inspection to identify damage such as cracks or defects on the sharp syndesmotome. Due to its design and the materials used, there is no defined maximum limit for processing cycles, but the use of damaged or worn products is formally prohibited.

Who is the manufacturer and what standards are met?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device in accordance with current regulations. The manufacturer imposes strict protocols for reprocessing and verification of compatibility with other products. As a Class I instrument, it meets the safety and performance requirements for manual dental instruments intended for oral surgery, subject to exclusive use by competent practitioners.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.