FDA Device Establishments · JSON-LD · Markdown
FEI 3029957137 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3029957137 |
|---|---|
| Owner / Operator | REEV (#10089096) |
| Address | 445 l'Occitane, Labege Haute-Garonne, 31670, FR |
| Mandatory US Agent | REEV |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQX |
| Regulation § (21 CFR) | 888.1500 |
| Proprietary names | Reev Sense |
Source: openFDA. Public-domain (CC0).