FDA Device Establishments · JSON-LD · Markdown
FEI 3006543086 · Manufacture Medical Device · Status: Active
| FEI Number | 3006543086 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | 7 rue Frederic Degeorge, Bat B 2ieme etage, ARRAS Pas-de-Calais, 62028, FR |
| Mandatory US Agent | Beckman Coulter, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JQP |
| Regulation § (21 CFR) | 862.2100 |
| Proprietary names | AutoMate 2550 Sample Processing System; AutoMate 2500 Sample Processing System; ODL25125 AutoMate 1250 LAB INSTRUMENT; AutoMate 1250 Sample Processing System; AutoMate 1200 Sample Processing System; ODL25120 AutoMate 1200 LAB INSTRUMENT; A18896 Automate 600 Sample Processing System; ODL25250 AutoMate 2500 LAB INSTRUMENT; A18894 Automate 800 Sample Processing System; Command Central |
Source: openFDA. Public-domain (CC0).