# Beckman Coulter Biomedical GmbH

FEI: 3021394862
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: BECKMAN COULTER, INC. (#2050012)

Address: Kuehler Weg 1, Baierbrunn Bavaria, 82065, DE

Mandatory US Agent: Beckman Coulter, Inc.

## Products

Total registered: 1
Top product codes: JQP
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223021394862%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3021394862