FDA Device Establishments · JSON-LD · Markdown
FEI 3011080315 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3011080315 |
|---|---|
| Owner / Operator | Numares AG (#10088504) |
| Address | Am BioPark 13, Regensburg Bavaria, 93053, DE |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MRR |
| Regulation § (21 CFR) | 862.1475 |
| Proprietary names | AXINON® LDL-p Test System |
Source: openFDA. Public-domain (CC0).