Dental extraction cable for Benex system, length 50 cm - Helmut Zepf (12.321.50) - Delynov

What is the dental extraction cable for the Helmut Zepf Benex system?

The dental extraction cable, referenced under code 12.321.50 by Helmut Zepf Medizintechnik GmbH, is a specific component designed to integrate with the Benex extraction system. This device is presented as a flexible cable with a length of 50cm, developed to withstand mechanical stress during traction phases. As a Benex extraction accessory, its structure is optimized to guarantee reliable force transmission between the extractor and the anchor screw fixed in the root. This equipment is intended exclusively for professional use in oral surgery to facilitate the removal of dental elements while preserving the integrity of the socket and surrounding tissues.

What are the clinical indications for this dental extractor cable?

This Benex cable is indicated in all clinical situations requiring controlled vertical extraction, particularly when preservation of the vestibular bone plate is critical, such as in cases of immediate loading or pre-programmed implant surgery. It is used by dental surgeons for the avulsion of residual roots or teeth whose coronal structure is compromised. By allowing an atraumatic extraction, this cable limits collateral damage to periodontal tissues. Its use is common during complex procedures where conventional extraction methods using forceps or elevators might risk a fracture of the alveolar wall.

What are the technical characteristics of cable 12.321.50?

The Helmut Zepf extraction cable (reference 12.321.50) has a total length of 50cm, offering sufficient range of motion for manipulating the extractor in the mouth. Its technical design is based on high flexibility combined with the tensile strength essential for the Benex system. The cable termination is configured to adapt precisely to the other components of the Helmut Zepf brand extraction kit, thus ensuring operational safety during the surgical procedure. Its thinness and robustness allow traction forces to be passed axially, avoiding tipping movements that could damage the alveolar bone.

What are the contraindications for using this extraction accessory?

The contraindications for using this cable are related to the intrinsic limits of the vertical extraction system. It should not be used if the anchoring of the screw in the root is not deemed sufficient to support the traction force, or if the root morphology presents extreme curvatures or ankylosis making axial extraction impossible without risk of major fracture. In general, the use of this equipment is contraindicated in patients presenting uncontrolled systemic pathologies interfering with bone healing or in cases of untreated acute infection at the surgical site. One should systematically refer to the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH before any intervention.

What are the maintenance and durability precautions for this cable?

As a device used in a surgical environment, this dental extraction cable must be subject to a rigorous cleaning, disinfection, and sterilization protocol in accordance with the instructions from manufacturer Helmut Zepf. Although designed to withstand repeated traction cycles, the integrity of the cable must be visually inspected before each intervention. Any sign of fraying, corrosion, or permanent deformation requires immediate replacement of the part to avoid any intraoperative breakage. Careful handling during placement on the extractor helps extend the life of the device and maintain the precision of the Benex system.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-precision dental instrumentation. Although the specific regulatory class and CE marking are not detailed in the current source data, Helmut Zepf products are generally designed according to high quality standards specific to the German medical industry. To obtain precise information on certificates of conformity, applied ISO standards, or CE marking details for reference 12.321.50, it is imperative to consult the official technical documentation provided by the manufacturer or refer to the product labeling upon receipt.

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