FDA Device Establishments · JSON-LD · Markdown
FEI 3014200871 · Manufacture Medical Device · Status: Active
| FEI Number | 3014200871 |
|---|---|
| Owner / Operator | Adria Srl. (#10062522) |
| Address | Via Modena n. 46, San Giovanni in Persiceto Bologna, 40017, IT |
| Mandatory US Agent | Dumotech, LLC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OCJ |
| Regulation § (21 CFR) | 888.4540 |
| Proprietary names | Vertebroplasty Canulated Needle - 493xx, T0604xx; Vertebroplasty Needle Kit - 49225; Vertebroplasty Needle - 496xx, 498xx, 491xx, 490xx, 492xx, T0604xx |
Source: openFDA. Public-domain (CC0).