EUDAMED last updated this device on May 23, 2026
3713
B-42607708207890On the marketClass IIb
- Applicable legislation
- —
- Organization name
- Intermedt Medizin & Technik 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 →- 42607708207890
- Reference / catalog number
- 3713
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.
3713 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Intermedt Medizin & Technik GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.