Selected Product Technical Facts
- Identity and scope: Medical-application robotic arm displayed on the China website. A product page does not establish medical-product authorization for a particular intended use or country. Product page.
- Evidence limit: The supplied record does not provide a separate detailed technical parameter set. Diana 7 specifications are not copied here. The page's IEC 60601-1 / IEC 60601-1-2 statements are not a substitute for applicable registration documents or model-specific certification evidence.
Company Integration & Application Notes
Source-disclosed interfaces: Diana 7 has controller Modbus-TCP/TCP/IP/RS232 and source-announced FCI support; Thor 7 Pro has controller TCP/IP/Modbus-TCP/RS232; the Tekken D base configuration uses RS485/Modbus RTU. A shared protocol name, group affiliation or placement on the same website is not evidence that two products connect directly. Diana 7, FCI announcement, Thor 7 Pro, Tekken D.
System validation still required: Confirm mechanical mounting, tool-power budget, communication roles/registers/API, version matching, real-time behavior, emergency-stop/safety circuits, actual load and acceptance tests for the delivered system. For Diana 7 Med, obtain current product authorization and intended-use/region evidence separately. IEC 60601-1 / IEC 60601-1-2 statements on a product page do not replace applicable registration or model-specific certification evidence. Diana 7 Med.
Configuration and attribution boundary: Keep Tekken D, Tekken D+ VT10-G and the independent VT10-G record separate. Group-site Agile Hand and AgileCore are not attributed as Beijing-manufactured products. Quotation, manufacturing location, contracting entity, delivery batch and after-sales responsibility require procurement documents, not inference from a website footer. Thor 20's China listing and group Coming soon status must both be considered. Tekken configurations, Independent sensor, Thor 20, Group Thor series.
Before You Evaluate or Order
- Request current medical-product registration or authorization for the exact model, intended use and destination region.
- Obtain model-specific technical, electrical and safety documents rather than substituting the standard Diana 7 specification.
- Confirm the evidence supporting applicable standards statements and agree validation responsibilities for the intended medical system.
These points require confirmation for your intended purchase and application. Missing public information does not imply a product deficiency.