EUDAMED last updated this device on Jun 24, 2026
DK50 DI
B-08586014620929On the marketClass IIa
- Applicable legislation
- —
- Organization name
- EKOM spol. s r.o.
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 →- 08586014620929
- Reference / catalog number
- 430700019-102
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.
DK50 DI is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by EKOM spol. s r.o.. Placed on the EU market in Slovakia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.