FDA Device Establishments · JSON-LD · Markdown
FEI 3039404452 · Manufacture Medical Device · Status: Active
| FEI Number | 3039404452 |
|---|---|
| Owner / Operator | TECHNOFLEX SAS (#10093662) |
| Address | 69 ZA deBassilour, BIDART Nouvelle-Aquitaine, 64210, FR |
| Mandatory US Agent | mdi Consultants, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KPE |
| Regulation § (21 CFR) | 880.5025 |
Source: openFDA. Public-domain (CC0).