FDA Device Establishments · JSON-LD · Markdown
FEI 3001779742 · Manufacture Medical Device · Status: Active
| FEI Number | 3001779742 |
|---|---|
| Owner / Operator | DPM USA CORP. (#9008401) |
| Address | 1460 N.W. 107TH AVE., STE. G, Doral, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EFA |
| Regulation § (21 CFR) | 872.4200 |
| Proprietary names | Tubinetta Fit Lux, Tubinetta Ultra, Switch E, Bogotta Light Plus, Bogota Stilla Prime |
Source: openFDA. Public-domain (CC0).