# TECHNIX SPA

FEI: 3008044777
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: TECHNIX S.P.A. (#10048870)

Address: Via E. Fermi, 45, Grassobbio Bergamo, 24050, IT

Mandatory US Agent: Dornier MedTech America

## Products

Total registered: 1
Top product codes: JAA
Regulation §: 892.1650

Proprietary names: Nautilus

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008044777%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008044777