# Baxter R&D Europe SPRL

FEI: 1000359047
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: BAXTER HEALTHCARE CORPORATION (#1417572)

Address: Boulevard d'Angleterre 2-4, Braine-l'Alleud Wallonia, 1420, BE

Mandatory US Agent: Baxter Healthcare Corporation

## Products

Total registered: 1
Top product codes: FMF
Regulation §: 880.5860

Proprietary names: Duploject, Due Set A, Duo Set

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000359047%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000359047