FDA Device Establishments · JSON-LD · Markdown
FEI 3010862420 · Manufacture Medical Device for Another Party (Contract Manufacturer) Complaint File Establishment per 21 CFR 820.198 Sterilize Medical Device for Another Party (Contract Sterilizer) Remanufacture Medical Device Repack or Relabel Medical Device Foreign Private Label Distributor Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility Reprocess Single-Use Device Manufacture Medical Device · Status: Active
| FEI Number | 3010862420 |
|---|---|
| Owner / Operator | EVO DI BRIDDA MASSIMO (#10046465) |
| Address | VIA FELTRE 52/M, SEDICO Belluno, 32036, IT |
| Mandatory US Agent | THE VISION COUNCIL |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQY |
| Regulation § (21 CFR) | 886.5850 |
Source: openFDA. Public-domain (CC0).