EUDAMED last updated this device on Jul 17, 2026
011
805099952STRUMGY3On the marketClass I
- Applicable legislation
- —
- Organization name
- Errecieffe 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 →- 08057635221883
- Reference / catalog number
- 011
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.
011 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Errecieffe srl. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.