EUDAMED last updated this device on Mar 17, 2026
LIOLI-rD
B-00814899027358On the marketClass IIa
- Applicable legislation
- —
- Organization name
- AST VisionCare Inc.
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 →- 00814899027358
- Reference / catalog number
- LIOLI-rD
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.
LIOLI-rD is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by AST VisionCare Inc.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.