FDA Device Establishments · JSON-LD · Markdown
FEI 1950204 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 1950204 |
|---|---|
| Owner / Operator | BIOMERIEUX SA (#8020790) |
| Address | 595 ANGLUM RD., HAZELWOOD, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | LON |
| Regulation § (21 CFR) | 866.1645 |
| Proprietary names | VITEK 2 GP AST for Cefotaxime |
Source: openFDA. Public-domain (CC0).