# FISIOLINE S.R.L.

FEI: 3004027973
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: FISIOLINE S.R.L. (#9073583)

Address: BORGATA MOLINO 29, VERDUNO Cuneo, 12060, IT

Mandatory US Agent: LASER BIOTECH INTERNATIONAL

## Products

Total registered: 1
Top product codes: ILY
Regulation §: 890.5500

Proprietary names: LUMIX ULTRA 1, LUMIX ULTRA 3, LUMIX ULTRA 2

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004027973%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004027973