FDA Device Establishments · JSON-LD · Markdown
FEI 3019252624 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3019252624 |
|---|---|
| Owner / Operator | Acarix AS (#10081966) |
| Address | Ryvangs Alle 81-83, Hellerup Hovedstaden, DK-2900, DK |
| Mandatory US Agent | Acarix USA Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QMW |
| Regulation § (21 CFR) | 870.1420 |
| Proprietary names | CADScor System |
Source: openFDA. Public-domain (CC0).