Zygoguide Length: 170mm Diameter: 6mm - Landanger - J245203 - Delynov

What is the zygoguide from the brand Landanger?

The zygoguide is a specialized surgical instrument distributed by Delynov, designed by the manufacturer to assist practitioners during the critical phases of implantology. This device features an optimized structure with a length of 170mm and a diameter of 6mm. As an instrument in the CONSO category, it is specifically developed to meet the requirements of complex oral surgery. Its robust design allows for precise handling during implant site preparation, offering a reliable solution for guiding cutting instruments into deep bone structures. The brand Landanger ensures manufacturing that meets the professional standards required for this type of zygomatic implantology accessory.

What are the clinical indications for this instrument?

The zygoguide is primarily indicated for implant surgery interventions involving the zygomatic bone. Its use is recommended when the practitioner must achieve precise guidance during drilling in complex anatomical areas where visibility or access is restricted. It integrates perfectly into zygomatic implant placement protocols for patients with severe maxillary atrophy. This zygoguide instrument helps secure the drilling trajectory, thereby limiting the risks of deviation during the creation of the implant site. It is intended exclusively for professional use by dental surgeons, stomatologists, or maxillofacial surgeons trained in these specific rehabilitation techniques.

What are the technical characteristics of the zygoguide j245203?

The model j245203, produced by the manufacturer under the brand Landanger, presents rigorous technical specifications for implantology. It has a total length of 170mm, which allows for reaching posterior and superior areas with increased ease. Its diameter of 6mm is calibrated to offer optimal stability while remaining compatible with the space constraints of the oral cavity. This CONSO category instrument is designed to withstand the mechanical stresses associated with drill guidance. The Landanger reference j245203 guarantees traceability and manufacturing quality consistent with the expectations of operating rooms specialized in oral and implant surgery.

What are the contraindications for the use of this instrument?

The contraindications for using the zygoguide are primarily related to the limits of zygomatic surgery techniques themselves. Its use is prohibited in cases of untreated local bone pathologies, active infections at the surgical site, or acute maxillary sinusitis. Furthermore, the use of this instrument by unqualified personnel or those not trained in zygomatic implantology protocols constitutes a major contraindication. It is imperative to check the integrity of the instrument before each use; any visible deformation or damage must lead to its immediate removal from the clinical circuit to ensure patient safety and the precision of the surgical procedure.

What are the maintenance precautions for this non-resorbable device?

As it is a metallic surgical instrument of the zygoguide type, it is not subject to resorption. Precautions for use include rigorous cleaning and sterilization in accordance with current protocols for reusable medical devices, unless otherwise stated by the manufacturer. Decontamination cycles must be scrupulously followed to avoid any corrosion or accumulation of biological residues. Storage must be carried out in a dry and clean environment. The brand Landanger recommends following the specific cleaning instructions provided in the technical manual to preserve the mechanical properties of the guide, particularly its straightness and its diameter of 6mm, which are essential for the precision of the zygomatic drilling guide.

Who is the manufacturer and what standards are respected?

The zygoguide bearing reference j245203 is produced by the manufacturer and distributed under the brand Landanger. Although the regulatory class and specific CE marking are not detailed in the current source data, this device belongs to the CONSO category of surgical instruments. As an instrument intended for invasive surgery, it is manufactured according to controlled industrial processes guaranteeing its compliance with the requirements of modern implantology. Practitioners are invited to consult the product labeling and the instructions for use attached by the manufacturer to obtain details regarding compliance certifications and specific safety standards in force at the time of marketing.

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