EUDAMED last updated this device on Jun 9, 2026
SPIRO Humidifier
B-07350061230001On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Fogless International AB
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 →- 07350061230001
- Reference / catalog number
- 702
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.
SPIRO Humidifier is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Fogless International AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.