EUDAMED last updated this device on Jun 28, 2026
Actolind w Solution 5x10 ml monodose tube
B-04250108306719On the marketClass III
- Applicable legislation
- —
- Organization name
- ACTO GmbH
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 →- 04250108306719
- Reference / catalog number
- 06.6703.05M10
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.
Actolind w Solution 5x10 ml monodose tube is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by ACTO GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.