FDA Device Establishments · JSON-LD · Markdown
FEI 3024706750 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3024706750 |
|---|---|
| Owner / Operator | Keri Medical (#10085771) |
| Address | Chemin du Pre-Fleuri 5, Plan-les-Ouates Geneve, 1228, CH |
| Mandatory US Agent | Nilson Law Group |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FSM |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | Kirschner wire Tube |
Source: openFDA. Public-domain (CC0).