MDR Information and Recommendations

European Medical Device Regulation (MDR) information page providing guidance on MDR compliance, UDI (Unique Device Identification) system implementation, and VITA quality standards. Includes information about veneering and CAD/CAM materials, prosthetic teeth labeling, documentation requirements, and tooth set descriptions (VITAPAN EXCELL, VITA LINGOFORM, VITAPAN PLUS, VITAPAN, VITAPAN CUSPIFORM, VITA PHYSIODENS, VITAPAN SYNOFORM, LUMIN VACUUM, VITA PHYSIODENS). Also covers documentation options and declarations of conformity access through MyVITA portal.