FDA Device Establishments · JSON-LD · Markdown
FEI 3004530258 · Manufacture Medical Device · Status: Active
| FEI Number | 3004530258 |
|---|---|
| Owner / Operator | CEPHEID (#9062742) |
| Address | 904 CARIBBEAN DRIVE, Sunnyvale, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QQX |
| Regulation § (21 CFR) | 866.3981 |
| Proprietary names | Xpert® Xpress CoV-2 plus |
Source: openFDA. Public-domain (CC0).