EUDAMED last updated this device on May 27, 2026
EMAM
++EMICFAM1RIN4HOn the marketClass IIa
- Applicable legislation
- —
- Organization name
- Micerium S.p.A.
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 →- EMICEMAM1
- Reference / catalog number
- EMAM
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.
EMAM is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Micerium S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.