FDA Device Establishments · JSON-LD · Markdown
FEI 3002504068 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3002504068 |
|---|---|
| Owner / Operator | C. R. Bard, Inc. (#2212754) |
| Address | Hagelberg 2, Olen Antwerpen, 2250, BE |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FGE |
| Regulation § (21 CFR) | 876.5010 |
| Proprietary names | LifeStent XL Biliary Stent System; LifeStent Biliary Stent System |
Source: openFDA. Public-domain (CC0).