EUDAMED last updated this device on Jul 13, 2026
Lotupharma
805059387INRLOG2024CCOn the marketClass I
- Applicable legislation
- —
- Organization name
- Logiter One Srl
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 →- 08050593878076
- Reference / catalog number
- INR02
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.
Lotupharma is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Logiter One Srl. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.