Surgical tip holder according to Lindo Leviendroit, 3.0mm tip - Helmut Zepf (17.007.06LL) - Delynov

What is the surgical tip holder according to Lindo Leviendroit?

The surgical tip holder according to Lindo Leviendroit is a specialized manual instrument designed by Helmut Zepf Medizintechnik GmbH. This device is specifically configured to receive and lock a 3.0 mm tip, thus forming a functional assembly for extraction surgery. Its structure is designed to offer a rigid and secure grip, allowing the practitioner to apply the necessary force vectors during oral surgery procedures. As a component of the Helmut Zepf modular system, this tip holder (reference 17.007.06LL) guarantees a stable interface between the surgeon's hand and the working part of the instrument.

What are the clinical indications for this instrument?

This instrument is primarily indicated for complex dental extractions and alveolar surgeries. Used as a Lindo elevator, it serves for the luxation of roots and the avulsion of teeth where access or resistance requires specific mechanical support. Its use is common in implantology and oral surgery during site preparation or the clearance of impacted or embedded dental structures. The practitioner uses this surgical tip holder to mobilize the dental element before its final removal, relying on lever principles adapted to the morphology of the alveolar bone.

What are the technical characteristics of the 17.007.06LL tip holder?

The Helmut Zepf surgical tip holder, bearing technical reference 17.007.06LL, is characterized by an internal housing calibrated for a 3.0 mm tip. Its design is based on the work of Lindo Leviendroit, aiming to optimize ergonomics during the force phases of oral surgery. The instrument is designed to withstand the torsional and pressure stresses exerted during luxation. The surface finish is developed to limit reflections under operating lights while facilitating cleaning protocols. The connection between the handle and the tip is designed to avoid any mechanical play, ensuring direct transmission of tactile sensitivity to the surgeon.

What are the contraindications for the use of this tip holder?

Contraindications for the use of the Helmut Zepf surgical tip holder are related to the limits of the manual elevation technique. It must not be used if the surrounding bone exhibits excessive fragility or a bone pathology that does not allow for a stable fulcrum. The use of tips whose diameter or connection does not strictly correspond to the 3.0 mm specification of this tip holder is prohibited to avoid any risk of breakage or intraoperative detachment. Generally, the instrument must not be used outside of the surgical procedures for which it was designed, nor on patients with general contraindications to oral surgery.

What are the maintenance and sterilization precautions?

As a non-resorbable instrument intended for repeated use, this surgical tip holder must undergo a complete cycle of decontamination, cleaning, and sterilization between each patient. It is recommended to follow steam sterilization protocols (autoclave) in accordance with the instructions from the manufacturer Helmut Zepf Medizintechnik GmbH. Particular attention must be paid to cleaning the tip connection area to eliminate all organic residues. Before each procedure, the practitioner must check for the absence of corrosion, cracks, or deformation on the instrument body and ensure the perfect locking of the 3.0 mm tip.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-precision surgical instrumentation. Although specific details of the regulatory class or CE marking are not mentioned in the simplified technical documentation, Helmut Zepf products are generally designed according to the rigorous quality standards of the German medical industry. For any precise information regarding certifications, ISO standards, or compliance with the European Medical Device Regulation (MDR), it is imperative to refer to the instructions for use and the original labeling provided by the manufacturer with the instrument.

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