FDA Device Establishments · JSON-LD · Markdown
FEI 2122870 · Manufacture Medical Device · Status: Active
| FEI Number | 2122870 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | 1000 LAKE HAZELTINE DR., CHASKA, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | CFL |
| Regulation § (21 CFR) | 862.1370 |
| Proprietary names | Access Ultrasensitive hGH (P/N: 33580) |
Source: openFDA. Public-domain (CC0).