FDA Device Establishments · JSON-LD · Markdown
FEI 3008629785 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3008629785 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | 2295 Progress Dr., Suite C, Hebron, KY, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GGK |
| Regulation § (21 CFR) | 864.8540 |
| Proprietary names | IRIS BODY FLUIDS LYSING REAGENT; PerFix NC Kit (Lysing Reagent); IOTest 3 Fixative; Reagent 2: Permeabilization; Lysing Solution (10X); VersaLyse : Lysing Solution; IntraPrep; AQUIOS Lysing Reagent Kit; OptiLyse C : Lysing Solution; Fixative Solution (10X) |
Source: openFDA. Public-domain (CC0).