EUDAMED last updated this device on Jul 3, 2026
AD Plus
B-08055348433364On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Meika Group S.r.l.
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 →- 08055348433364
- Reference / catalog number
- SEP3092-01
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.
AD Plus is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Meika Group S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.