FDA Device Establishments · JSON-LD · Markdown
FEI 3002900744 · Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3002900744 |
|---|---|
| Owner / Operator | I.O.V.E.S. SPA (#10044408) |
| Address | VIA DELL INDUSTRIA 9, LOZZO DI CADORE Belluno, 32040, IT |
| Mandatory US Agent | IOVES USA |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQZ |
| Regulation § (21 CFR) | 886.5842 |
| Proprietary names | AMARCORD; WEST; DIVA |
Source: openFDA. Public-domain (CC0).