These terms govern use of this Planmeca information site and inquiry workflow. Content is provided for business evaluation of dental and oral health equipment, service planning, technical documentation, and procurement discussions. It is not a clinical instruction, installation authorization, regulatory submission, or replacement for official IFU documentation supplied with a cleared or registered device.
When you submit an inquiry, you confirm that the information is accurate enough for routing to sales, service, clinical application, or documentation teams. A response may include general product information, specification sheets, room-planning notes, service options, or a request for additional details. No purchase agreement is created until a separate written quotation, acceptance, and applicable commercial terms are executed.
Documents, images, and descriptions on this site are for evaluation by dental practices, hospitals, laboratories, distributors, and procurement teams. You may share materials internally for review, but you may not modify, resell, misrepresent, or use them as device labeling. Availability, regulatory status, and specifications may vary by country, market, configuration, and software version.
Service response times, maintenance intervals, software support, and documentation packages depend on the final equipment configuration, location, contract tier, and local regulatory requirements. Dental equipment should be installed, operated, maintained, and serviced only according to applicable IFU, safety requirements, radiation safety rules, infection-control policies, and authorized service procedures.