FDA Device Establishments · JSON-LD · Markdown
FEI 3008044777 · Manufacture Medical Device · Status: Active
| FEI Number | 3008044777 |
|---|---|
| Owner / Operator | TECHNIX S.P.A. (#10048870) |
| Address | Via E. Fermi, 45, Grassobbio Bergamo, 24050, IT |
| Mandatory US Agent | Dornier MedTech America |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JAA |
| Regulation § (21 CFR) | 892.1650 |
| Proprietary names | Nautilus |
Source: openFDA. Public-domain (CC0).