EUDAMED last updated this device on Aug 13, 2026
DemeLON
B-10652927263784On the marketClass IIb
- 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 →- 10652927263784
- Reference / catalog number
- NL193019F13M
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.
DemeLON is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by DemeTECH Corp. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.