EUDAMED last updated this device on Jul 21, 2026
G-90010
4049368201APMOn the marketClass IIa
- Applicable legislation
- —
- Organization name
- Geuder AG
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 →- 04049368226031
- Reference / catalog number
- G-90010
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.
G-90010 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Geuder AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.