FDA Device Establishments · JSON-LD · Markdown
FEI 3007750372 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3007750372 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | Pelmolenlaan 15, Woerden Utrecht, 3447 GW, NL |
| Mandatory US Agent | Beckman Coulter, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GKZ |
| Regulation § (21 CFR) | 864.5220 |
| Proprietary names | DxH 520 Hematology Analyzer (B40602); DxH 560 Hematology Analyzer (B40603); DxH 500 Hematology Analyzer (B40601) |
Source: openFDA. Public-domain (CC0).