FDA Device Establishments · JSON-LD · Markdown
FEI 3020707080 · Manufacture Medical Device · Status: Active
| FEI Number | 3020707080 |
|---|---|
| Owner / Operator | FUJIFILM CORPORATION (#8031568) |
| Address | Medworkring 1, Hochstadt/Aisch Bavaria, 91315, DE |
| Mandatory US Agent | FUJIFILM Healthcare Americas Corporation |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GCE |
| Regulation § (21 CFR) | 878.4200 |
| Proprietary names | Application Catheter |
Source: openFDA. Public-domain (CC0).