EUDAMED last updated this device on Jul 29, 2026
DXQ04082120M
69437182RDXQTH2X- Applicable legislation
- —
- Organization name
- Beijing Demax Medical Technology Co.,Ltd.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 06943718225942
- Reference / catalog number
- DXQ04082120M
DXQ04082120M is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Beijing Demax Medical Technology Co.,Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.