# Beckman Coulter GmbH

FEI: 3002721051
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: BECKMAN COULTER, INC. (#2050012)

Address: Europark Fichtenhain B 13, Krefeld North Rhine-Westphalia, 47807, DE

Mandatory US Agent: Beckman Coulter, Inc.

## Products

Total registered: 1
Top product codes: GGK
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002721051%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002721051