EUDAMED last updated this device on Sep 10, 2026
UM-AURS2M1KJC
4981046CFA6607GHOn the marketClass I
- Applicable legislation
- —
- Organization name
- A&D Company, Limited
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 →- 04981046306607
- Reference / catalog number
- UM-AURS2M1KJC
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.
UM-AURS2M1KJC is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by A&D Company, Limited. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.