# Beckman Coulter Distribution B.V.

FEI: 3007750372
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: BECKMAN COULTER, INC. (#2050012)

Address: Pelmolenlaan 15, Woerden Utrecht, 3447 GW, NL

Mandatory US Agent: Beckman Coulter, Inc.

## Products

Total registered: 1
Top product codes: GKZ
Regulation §: 864.5220

Proprietary names: DxH 520 Hematology Analyzer (B40602), DxH 560 Hematology Analyzer (B40603), DxH 500 Hematology Analyzer (B40601)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007750372%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007750372