EUDAMED last updated this device on Aug 13, 2026
DemeLON
B-10652927729327On 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 →- 10652927729327
- Reference / catalog number
- NL1090040F2P
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 Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.