EUDAMED last updated this device on Sep 10, 2026
-213-6080
++EFOR020103DEOn the marketClass IIa
- Applicable legislation
- —
- Organization name
- Bernhard Förster 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 →- EFOR21360801
- Reference / catalog number
- -213-6080
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.
-213-6080 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Bernhard Förster GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.