# ACARIX AS

FEI: 3019252624
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Acarix AS (#10081966)

Address: Ryvangs Alle 81-83, Hellerup Hovedstaden, DK-2900, DK

Mandatory US Agent: Acarix USA Inc

## Products

Total registered: 1
Top product codes: QMW
Regulation §: 870.1420

Proprietary names: CADScor System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223019252624%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3019252624