XTool Syndesmotome - Helmut Zepf (17.008.08) - Delynov

What is the XTool syndesmotome - Helmut Zepf (17.008.08)?

The XTool syndesmotome, bearing reference 17.008.08, is a specialized manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from high-quality medical stainless steel, ensuring resistance adapted to the stresses of extraction surgery. Its structure is specifically studied to be inserted into the periodontal space to facilitate the initial mobilization of the tooth or root debris. As a Class I device, it meets the regulatory requirements for non-invasive or reusable surgical instruments after appropriate processing.

What are the clinical indications for this instrument?

The main use of the Helmut Zepf XTool syndesmotome lies in exodontia procedures. It is indicated for lifting teeth or extracting residual dental roots. In clinical practice, the practitioner uses it to sever the ligament fibers that hold the tooth in its socket. This step is crucial to reduce trauma to the surrounding tissues and facilitate subsequent bone expansion or the passage of forceps. Its application is essential in both conventional oral surgery and in site preparation for immediate implant surgeries.

What are the technical characteristics of model 17.008.08?

The XTool syndesmotome (reference 17.008.08) is distinguished by its medical stainless steel composition, a material chosen for its durability and its ability to withstand repeated sterilization cycles. This instrument is part of the XTool range developed by Helmut Zepf, recognized for its ergonomics adapted to precision interventions. Although it is delivered non-sterile by Helmut Zepf Medizintechnik GmbH, its design allows for complete cleaning and disinfection. There is no defined maximum limit of processing cycles, as longevity depends on the absence of visible damage such as cracks or defects on the cutting edges.

What are the contraindications for the use of this device?

The main medical contraindication related to the use of the XTool syndesmotome is hypersensitivity or intolerance to metals, specifically to the medical stainless steel used in its manufacture. If a hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be immediately stopped and the necessary clinical measures must be taken. Furthermore, the use of the instrument is strictly prohibited if it shows visible damage, breaks, or pronounced wear of the sharp edges, in order to avoid any risk of injury or intraoperative complication.

What are the maintenance and reprocessing precautions?

The XTool syndesmotome is a reusable instrument that requires a strict reprocessing protocol. According to the instructions of the manufacturer Helmut Zepf, all instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is essential to visually inspect the product before each intervention to detect any trace of wear, crack, or deformation. The use of damaged products is prohibited. The sterilization process must follow the standards in force for Class I devices to guarantee patient safety and the durability of the medical steel.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer in the field of dental instrumentation ensures the conformity of its products to safety and quality standards. The XTool syndesmotome is classified as a Class I medical device. In accordance with regulatory requirements, it is delivered non-sterile and its implementation is strictly reserved for qualified healthcare professionals. Compliance with the cleaning and sterilization protocols recommended by the manufacturer is essential to maintain the conformity of the device during its use in a dental office or hospital environment.

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