Establishment registration
BECKMAN COULTER, INC.
FDA establishment registration 1061932 · Miami, US
Key facts
| Registration number | 1061932 |
|---|---|
| Establishment name | BECKMAN COULTER, INC. |
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| FEI number | 3000203293 |
| Address | 11800 SW 147TH AVE. |
| City | Miami |
| State | FL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDM, CEN, GGK, GGL, GIF, GKG, GKL, GKZ, GTY, IFB, JCB, JHI, JIL, JIN, JIO, JIR, JJB, JJQ, JJW, JMA, JMT, JPI, JPK, JQC, JQP, JRE, JTC, KHE, KPA, KQC and 17 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database