EUDAMED last updated this device on Jun 24, 2026
MMT-385
0763000B00004147DOn the marketClass I
- Applicable legislation
- —
- Organization name
- Medtronic MINIMED
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 →- 00763000381080
- Reference / catalog number
- MMT-385
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.
MMT-385 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Medtronic MINIMED. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.