CE marking under the EU Medical Device Regulation (MDR) is the European regulatory access point and is frequently sought by Chinese manufacturers planning international expansion. It is also a common entry credential for international robotics companies establishing a Chinese market footprint, since CE data often supports subsequent NMPA submissions.
This list includes products in this database with a confirmed CE marking value. “Yes” or a year-month date both indicate confirmed marking; explicit “Not Applied” or empty values are excluded.
For context on how this data is sourced and refreshed, see data methodology.