EUDAMED last updated this device on Jul 2, 2026
Eamis lite™ system 123800
872016816123110HEOn the marketClass I
- Applicable legislation
- —
- Organization name
- MacroMedics
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 →- 08719425702483
- Reference / catalog number
- 123800
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.
Eamis lite™ system 123800 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MacroMedics. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.