Trium® 3D Panoramic Upgrade Ceph Right

Product Description

X-Mind Trium 1. Product Benefits • Superior Image Quality - X-MIND® TRIUM is equipped with an acquisition and reconstruction algorithm which ensures a perfectly uniform and high quality image on all visual axes. • High Level 3d Software - Acteon Imaging Suite (AIS) offers advanced functionalities and an intuitive mouse-enabled navigation experience. AIS is also fully compatible with MAC and PC so it functions in any environment. • Implant Planning - X-MIND TRIUM is a key tool for treatment planning and post-procedure follow-up. X-MIND TRIUM provides a fully comprehensive view of the patient’s arch. X-MIND TRIUM facilitates accurate evaluation of bone density and the positioning of the anatomic structures to be able to place implants more confidently. In addition to this, 3D imaging enables the size and shape of the implants to be made in proportion to the morphology of the patient. X-MIND TRIUM provides very clear and accurate images for transverse sections, the volume calculation of biomaterial needed for sinus elevation surgery and guided surgery with Acteon imaging Suite software 2. Main Characteristics • Full 360° Of Rotation • 75 Micrometer Image Quality • 4 F.O.V • Artifacts Reduction Filter • Full Implant Report in less than One Minute • Fully Upgradeable 3. Legal Notice - X-MIND TRIUM®, 3-in-1 extra-oral imaging device (3D CBCT, Panoramic and Cephalometric). - X-MIND trium is a class 3R laser product per IEC 60825-1:2007. Avoid direct eye exposure to laser radiation. Viewing the laser output with magnifying optical instruments (for example, surgical microscope and binocular glasses) may pose an eye hazard and thus the user should not direct the beam into an area where such instruments are likely to be used. This medical device is classified IIb according to the current applicable European Directive. It is CE marked. Notified Body: DNV GL NEMKO PRESAFE– CE 2460. It is a class II device according to 21 CFR 892.1750; product code OAS, MUH. This medical device dedicated to dental care is restricted to health staff; it is not reimbursed by health insurance organizations. This device was developed and manufactured according to the EN ISO 13485 Quality Management System and according to 21 CFR part 820 Quality System Regulation.