EUDAMED last updated this device on Jul 21, 2026
Actosed Endo 5 L
B-04250108301011On the marketClass IIb
- 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 →- 04250108301011
- Reference / catalog number
- 01.0101.5
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.
Actosed Endo 5 L is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ACTO GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.