EUDAMED last updated this device on Aug 13, 2026
DemeSILK
B-10652927803737On 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 →- 10652927803737
- Reference / catalog number
- SK262030H2P
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.
DemeSILK 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.