FDA Device Establishments · JSON-LD · Markdown
FEI 3007120545 · Develop Specifications But Do Not Manufacture At This Facility Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3007120545 |
|---|---|
| Owner / Operator | KERVIEW S.A. (#10052756) |
| Address | Ituzaingo 1309 Office 101, MONTEVIDEO, 11000, UY |
| 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).