# Philips North America LLC

FEI: 3006648320
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Philips Medical Systems International BV (#1217116)

Address: 222 Jacobs Street, Cambridge, MA, US



## Products

Total registered: 4
Top product codes: DQA, DXN, FLL, MWI
Regulation §: 870.2700, 870.1130, 880.2910, 870.2300

Proprietary names: SmartLinx Vitals Plus Patient Monitoring System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006648320%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006648320