EUDAMED last updated this device on May 11, 2026
UriSponge™
80533260CD0160AM0019KOn the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Copan Italia 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 →- 28053326000533
- Reference / catalog number
- 802CE.A
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.
UriSponge™ is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Copan Italia S.P.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.