FDA Device Establishments · JSON-LD · Markdown
FEI 1000191953 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1000191953 |
|---|---|
| Owner / Operator | Medica S.p.A. (#9040626) |
| Address | via degli Artigiani, 7, Medolla Modena, 41036, IT |
| Mandatory US Agent | Medica USA Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KDI |
| Regulation § (21 CFR) | 876.5860 |
| Proprietary names | Hemocor HP Hemoconcentrators - 400-1000-1400 + TS |
Source: openFDA. Public-domain (CC0).