EUDAMED last updated this device on Jul 6, 2026
MMT-305QS
0763000B000004472On 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 →- 00763000573690
- Reference / catalog number
- MMT-305QS
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-305QS 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.