Lindo surgical elevator, 3mm curved tip - Helmut Zepf (17.007.07LL) - Delynov

What is the surgical elevator according to Lindo Helmut Zepf?

The surgical elevator according to Lindo, referenced under code 17.007.07LL by Helmut Zepf, is a specialized manual instrument intended for oral surgery. This device is distinguished by a 3 mm working part with a curved tip, designed to adapt to the alveolar anatomy. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is structured to offer a rigid grip and controlled force transmission during luxation maneuvers. It is a tool of choice for practitioners seeking a reliable instrument for the preparation of simple or complex extractions in dental offices or hospital settings.

What are the clinical indications for this surgical dental elevator?

This surgical dental elevator is primarily indicated for the luxation of teeth and residual roots. In oral and implant surgery, it is used to separate the tooth from its alveolar attachment by applying moderate lever pressure. The 3 mm curved tip allows the instrument to slide along the root, facilitating the expansion of the alveolus. Its use is particularly relevant during the extraction of single-rooted teeth or to initiate the mobilization of molars before using forceps. It helps preserve the integrity of the surrounding bone walls by concentrating the force on the periodontal ligament.

What are the technical characteristics of reference 17.007.07LL?

The Helmut Zepf elevator (reference 17.007.07LL) features precise technical specifications to meet the requirements of oral surgery. Its major characteristic is its 3 mm wide tip, whose curvature is specifically studied according to the Lindo model to improve access to difficult areas. The monobloc design ensures the robustness necessary to withstand the mechanical stresses associated with elevation. The finish of the working part is optimized to guarantee smooth insertion without excessive slipping. This instrument is designed to be integrated into a standard autoclave sterilization protocol, in accordance with current hygiene practices in dental surgery offices.

What are the contraindications for the use of this instrument?

The contraindications for the use of the elevator according to Lindo are mainly related to the patient's clinical condition and the intervention area. It should not be used if the practitioner does not have sufficient visibility or if the alveolar bone exhibits extreme fragility (severe osteoporosis, history of radiotherapy) risking a fracture of the bone plate. Furthermore, its use is prohibited in cases of known allergy to the metals constituting the instrument, although these are standard in surgical environments. Applying excessive force without a stable fulcrum can also constitute a technical contraindication to avoid any damage to adjacent teeth or surrounding soft tissues.

What are the maintenance precautions for this non-absorbable instrument?

As a reusable and non-absorbable surgical instrument, this Helmut Zepf elevator requires a rigorous maintenance protocol after each intervention. It must be cleaned, decontaminated, and sterilized according to the instructions from the manufacturer Helmut Zepf Medizintechnik GmbH. It is recommended to use pH-neutral cleaning solutions to preserve the surface condition of the steel and avoid any corrosion. Before each sterilization cycle, a visual inspection of the 3 mm tip is necessary to ensure the absence of micro-cracks or deformations. Storage in a dry and protected environment is essential to guarantee the longevity of the instrument and patient safety during subsequent care.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a recognized company in the field of high-precision dental instrumentation. Although specific details of the regulatory class or CE marking are not explicitly mentioned in the provided technical documentation, Helmut Zepf products are generally manufactured according to high quality standards specific to the German medical industry. Practitioners are invited to systematically refer to the product labeling and the enclosed instructions for use to verify current certifications and specific safety instructions. For any additional information on compliance, consulting the manufacturer's official catalog is recommended.

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