# ALIFAX SRL

FEI: 3006988008
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: ALIFAX SRL (#10035224)

Address: Via Merano 30, Nimis Udine, 33045, IT

Mandatory US Agent: ISOPLAN USA

## Products

Total registered: 1
Top product codes: GKB
Regulation §: 864.5800

Proprietary names: SI 305.402-A LATEX CALIBRATORS, SI 305.302-A LATEX CONTROLS (30 TESTS), SI 305.100-A LATEX CONTROLS (6 TESTS), SI 804.100 JO-PLUS, SI 305.400-A LATEX CALIBRATORS, SI 195.210/THL TEST1 2, SI R20-PN ROLLER 20, SI R20-MC ROLLER 20, SI 305.300-A LATEX CONTROLS (30 TESTS), SI 305.102-A LATEX CONTROLS (6 TESTS)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006988008%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006988008