EUDAMED last updated this device on Aug 14, 2026
DemeSORB
B-10652927188537On the marketClass III
- Applicable legislation
- —
- Organization name
- DemeTECH Corp
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 →- 10652927188537
- Reference / catalog number
- PGA280240B0P
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
DemeSORB is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by DemeTECH Corp. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.