FDA Device Establishments · JSON-LD · Markdown
FEI 1000305841 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 1000305841 |
|---|---|
| Owner / Operator | QuidelOrtho Corporation (#2024674) |
| Address | 1000 LEE RD., Rochester, NY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 3 |
| Product codes (top 20) | MRR, JIT, JJX |
| Regulation § (21 CFR) | 862.1475, 862.1150, 862.1660 |
| Proprietary names | VITROS dLDL Reagent; VITROS Calibrator Kit 19; VITROS Performance Verifiers |
Source: openFDA. Public-domain (CC0).