FDA Device Establishments · JSON-LD · Markdown
FEI 3010749841 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3010749841 |
|---|---|
| Owner / Operator | BioGX (#10054546) |
| Address | 2450 Valleydale Rd, Birmingham, AL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OZX |
| Regulation § (21 CFR) | 866.3980 |
| Proprietary names | BioGX - Mycoplasma-Ureaplasma - OSR for BD MAX |
Source: openFDA. Public-domain (CC0).