FDA Device Establishments · JSON-LD · Markdown
FEI 3003249380 · Manufacture Medical Device · Status: Active
| FEI Number | 3003249380 |
|---|---|
| Owner / Operator | Citieffe srl (#10040297) |
| Address | Via Armaroli 21, Calderara di Reno Bologna, 40012, IT |
| Mandatory US Agent | THEMA CORP |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | JDW, KTT |
| Regulation § (21 CFR) | 888.3040, 888.3030 |
| Proprietary names | Dolphix® External Fixation System MR Conditional; DOLPHIX® EX.FIX.SYS. MR CONDITIONAL |
Source: openFDA. Public-domain (CC0).