Establishment registration
BECKMAN COULTER, INC.
FDA establishment registration 2050012 · BREA, US
Key facts
| Registration number | 2050012 |
|---|---|
| Establishment name | BECKMAN COULTER, INC. |
| Owner/operator | BECKMAN COULTER, INC. |
| Owner/operator number | 2050012 |
| FEI number | 2050012 |
| Address | 250 S Kraemer Blvd |
| City | BREA |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDQ, CDS, CDT, CEK, CEM, CEO, CFJ, CFN, CFR, CGA, CGN, CGS, CGX, CGZ, CHH, CHI, CHL, CHW, CIG, CIT, CIX, CJE, CJW, CJY, CKA, CZP, CZW, DAD, DBF, DBI and 98 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- 10–99 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