What are the clinical indications for this micro-screw system?

The indications for using the Meisinger micro-screw system primarily concern the secure fixation and stabilization of cortical bone transplants. This device is indicated for the treatment of bone fractures and proves particularly effective for fixing bone blocks transplanted during augmentation processes in the oral cavity or in the maxillo-mandibular intervention area. It allows the graft to be kept immobile throughout the healing phase, thus facilitating the integration of the autologous bone or transplant. These Micro Screw systems are essential for Guided Bone Regeneration (GBR) procedures requiring precision osteosynthesis.

What are the technical characteristics of the screws?

The system is distinguished by the technical finesse of its components. The major feature lies in the osteosynthesis screws which come in diameters of 1.0 mm and 1.2 mm. Despite these reduced dimensions, the surgical stainless steel alloy guarantees the mechanical strength necessary for the stabilization of cortical blocks. The reference code for this basic system is 79BMSBA. To ensure correct and safe use, the manufacturer Hager & Meisinger GmbH specifies that the recommended and maximum application speeds, summarized in the instrument overview in the "Contents" chapter, must be strictly respected by the surgeon during placement.

What are the contraindications for the use of this device?

The use of this osteosynthesis system is subject to compliance with general and local medical contraindications related to dental surgery. Absolute contraindications include active infections in or near the augmentation area, as well as local or systemic pathological processes such as fever, local inflammation, or abscesses. Use is also prohibited in cases of insufficient bone volume in terms of quality or quantity. Additionally, systemic or metabolic diseases, or drug treatments leading to progressive bone deterioration (such as the use of cortisone, immunosuppressants, bisphosphonates, or uncontrolled diabetes) constitute major contraindications.

What are the precautions regarding the duration of implantation?

It is important to note that the Micro Screws from the Meisinger range are not intended to remain permanently in the human body. They are temporary fixation devices. Once they have fulfilled their function of support and stabilization, particularly after complete healing of the bone transplant or consolidation of a fracture, they must be entirely removed during a secondary intervention. The practitioner must plan this removal to avoid any long-term interference. The safety of the intervention also depends on strict compliance with placement protocols, notably the rotation speeds of the instruments to preserve the integrity of the recipient site and the screw material.

Who is the manufacturer and what standards are met?

The basic micro-screw system is manufactured by Hager & Meisinger GmbH, located in Neuss, Germany. This medical device belongs to Class IIb, which reflects its level of regulatory requirement for invasive surgical interventions. It benefits from the CE0044 marking, guaranteeing its compliance with current European standards for medical devices (MDR). As a product distributed by Delynov, it meets the strictest quality standards for oral and maxillofacial surgery. The manufacturer insists that use must be reserved for trained professionals, scrupulously respecting the indications and warnings provided in the technical documentation.

Basic micro-screw system - Dr. Fouad Khoury - Meisinger - Hager & Meisinger GmbH (79BMSBA) - Delynov

Micro Screw System Basic - Dr. Fouad Khoury - Meisinger

Basic micro-screw system - Dr. Fouad Khoury - Meisinger - Hager & Meisinger GmbH (79BMSBA) - Delynov

Q: What is the Meisinger basic micro-screw system?

The basic micro-screw system, designed by Meisinger in collaboration with Dr. Fouad Khoury, is a medical device from the Bone Management® line dedicated to bone surgery. This system (reference 79BMSBA) is based on the use of specific osteosynthesis screws manufactured from surgical stainless steel. This material was selected to provide the screws with optimal stability despite their extremely reduced diameter. The structure of these micro-screws allows practitioners to perform bone fixation procedures with high precision. This complete kit is distributed by Delynov to meet the needs of dental and maxillofacial surgeons seeking a reliable solution for graft maintenance.

The Système de micro-vis basique - Dr. Fouad Khoury - Meisinger - Hager & Meisinger GmbH is a medical device manufactured by Hager & Meisinger GmbH — Class IIb, CE marking CE0044.

Compliance: Medical device Class IIb, CE marking CE0044.
Manufacturer: Hager & Meisinger GmbH.
Reference: 79BMSBA.
Reserved for healthcare professionals. Read instructions carefully before use.

956.00 € 956.0 EUR 956.00 € Tax Included 1,868.47 €

956.00 € Tax Included 1,868.47 €

Manufacturer

This combination does not exist.

Add to cart BUY NOW

GBR

What is the Meisinger basic micro-screw system (79BMSBA)?

The basic micro-screw system, developed in collaboration with Dr. Fouad Khoury and manufactured by Meisinger, is a specialized device for guided bone regeneration (GBR). This kit primarily consists of osteosynthesis screws designed in surgical stainless steel. This specific material was selected to offer optimal mechanical stability despite extremely reduced diameters of 1.0 mm and 1.2 mm. This Khoury micro-screw system allows practitioners to handle bone transplants with great precision, guaranteeing the rigid maintenance necessary for the initial bone healing phase. It is a robust technical solution for block graft management in the maxillofacial sector.

What are the clinical indications for this GBR micro-screw system?

The surgery micro-screw system from the Bone Management® line is specifically indicated for the secure fixation and stabilization of cortical bone transplants. Its main application concerns the treatment of bone fractures and, more frequently in the office, the fixation of bone blocks harvested and transplanted during augmentation processes in the oral cavity. These interventions aim to restore bone volume in the maxillomandibular area before or during implant placement. The use of this dental micro-screw system ensures strict immobilization of the graft, a sine qua non condition for successful bone integration and optimal revascularization of the cortical transplant.

What are the technical characteristics of the included screws?

The technical characteristics of this dental micro-screw system are based on the fineness and resistance of its components. The osteosynthesis screws are available in two distinct diameters: 1.0 mm and 1.2 mm. They are manufactured from a surgical grade stainless steel that provides high resistance to torsion and breakage, allowing their insertion even in sites with high bone density. As a Class IIb device, this system meets strict safety requirements. It is important to note that to guarantee correct use, the practitioner must respect the rotation speeds recommended by Meisinger in the instrument overview provided with the kit.

What are the contraindications for the use of this osteosynthesis kit?

The use of the Meisinger basic micro-screw system is subject to compliance with general and local medical contraindications related to oral surgery. Absolute contraindications include the presence of active infections in the augmentation area or its immediate periphery. Similarly, any uncontrolled local or systemic pathological process, such as fever, local inflammation, or abscesses, proscribes the intervention. Finally, insufficient bone volume, whether in terms of quality or quantity to ensure screw anchorage, constitutes a major contraindication. The practitioner must rigorously evaluate the physiological terrain before any implementation of the osteosynthesis protocol.

What are the precautions related to the removal of micro-screws?

Unlike permanent implants, the micro-screws of this system are not intended to remain indefinitely in the patient's body. Once the support and stabilization function is fulfilled — typically after complete healing of the bone transplant or consolidation of a fracture — the screws must be entirely removed. This removal generally occurs during the surgical reentry phase for implant placement. Prolonged maintenance beyond the healing phase is not recommended by the manufacturer Hager & Meisinger GmbH. The practitioner must therefore plan this removal step in their overall bone reconstruction treatment plan.

Who is the manufacturer and what standards are respected?

The basic micro-screw system (reference 79BMSBA) is manufactured by Hager & Meisinger GmbH, a recognized company located in Neuss, Germany. This medical device is certified according to current European standards, displaying a CE0044 marking. It belongs to the regulatory Class IIb, which guarantees a high level of quality control and safety for invasive oral surgery interventions. By choosing Meisinger products distributed by Delynov, dental surgeons and implantologists ensure they are using instruments that comply with the requirements of the European Medical Device Regulation, specifically designed for the demanding protocols of the Khoury technique.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer

Meisinger

Tags
Tags	GBR