EUDAMED last updated this device on Jul 10, 2026
OmniBoard™ BTM-SX-RE
872016816122500HQOn 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 →- 08719425705484
- Reference / catalog number
- 174540
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.
OmniBoard™ BTM-SX-RE is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MacroMedics. Placed on the EU market in Northern Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.