EUDAMED last updated this device on Aug 13, 2026
2030
89040452001RCOn the marketClass IIa
- Applicable legislation
- —
- Organization name
- Vitromed Healthcare
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 →- 00890404520309
- Reference / catalog number
- 2030
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.
2030 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Vitromed Healthcare. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.