EUDAMED last updated this device on May 19, 2026
P090804010202
B-08050880230518On the marketClass III
- Applicable legislation
- —
- Organization name
- Adler Ortho 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 →- 08050880230518
- Reference / catalog number
- 0101504
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.
P090804010202 is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by Adler Ortho S.p.A. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.