EUDAMED last updated this device on Aug 13, 2026
DemeQUICK
B-10652927673538On 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 →- 10652927673538
- Reference / catalog number
- PGR284017F13M
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.
DemeQUICK 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 Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.