EUDAMED last updated this device on Sep 4, 2026
Manu 3D
403276700000000004142S4On the marketClass I
- Applicable legislation
- —
- Organization name
- Ottobock SE & Co. KGaA
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 →- 04032767321445
- Reference / catalog number
- 4142=L-XXL-1
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.
Manu 3D is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Ottobock SE & Co. KGaA. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.