EUDAMED last updated this device on Jun 25, 2026
BTL SpiroAir
B-05407003163025On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Medisoft S.A.
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 →- 05407003163025
- Reference / catalog number
- SP-00-01-BTL
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.
BTL SpiroAir is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Medisoft S.A.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.