FDA Device Establishments · JSON-LD · Markdown
FEI 3016463905 · Manufacture Medical Device · Status: Active
| FEI Number | 3016463905 |
|---|---|
| Owner / Operator | EndoGI Medical, Ltd. (#10078370) |
| Address | Wadi El Haj 13, Nazareth Northern, 17111, IL |
| Mandatory US Agent | ProMedoss, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FGE |
| Regulation § (21 CFR) | 876.5010 |
| Proprietary names | X-Path Pre-loaded RX-OTW Double Biliary Stents System |
Source: openFDA. Public-domain (CC0).