# AIRSONETT AB

FEI: 3004793042
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Airsonett AB (#10027949)

Address: Kelliehousevagen 31, Angelholm Skane, 26274, SE

Mandatory US Agent: Pro Pharma Group

## Products

Total registered: 1
Top product codes: FRF
Regulation §: 880.5045

Proprietary names: Airsonett

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004793042%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004793042