FDA Device Establishments · JSON-LD · Markdown
FEI 3002806808 · Manufacture Medical Device · Status: Active
| FEI Number | 3002806808 |
|---|---|
| Owner / Operator | DIAGNOSTICS BIOCHEM CANADA, INC. (#8010132) |
| Address | 384 Neptune Crescent, London Ontario, N6M 1A1, CA |
| Mandatory US Agent | Regulatory Insight Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | CGF |
| Regulation § (21 CFR) | 862.1280 |
| Proprietary names | Estrone ELISA (CAN-E-420, CAN-E-420-8PK) |
Source: openFDA. Public-domain (CC0).