FDA Device Establishments · JSON-LD · Markdown
FEI 3004027973 · Manufacture Medical Device · Status: Active
| FEI Number | 3004027973 |
|---|---|
| Owner / Operator | FISIOLINE S.R.L. (#9073583) |
| Address | BORGATA MOLINO 29, VERDUNO Cuneo, 12060, IT |
| Mandatory US Agent | LASER BIOTECH INTERNATIONAL |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ILY |
| Regulation § (21 CFR) | 890.5500 |
| Proprietary names | LUMIX ULTRA 1; LUMIX ULTRA 3; LUMIX ULTRA 2 |
Source: openFDA. Public-domain (CC0).