FDA Device Establishments · JSON-LD · Markdown
FEI 3002721051 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3002721051 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | Europark Fichtenhain B 13, Krefeld North Rhine-Westphalia, 47807, DE |
| Mandatory US Agent | Beckman Coulter, Inc. |
| 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).