# Philips North America LLC

FEI: 1218950
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: Philips Medical Systems International BV (#1217116)

Address: 3000 Minuteman Rd, ANDOVER, MA, US



## Products

Total registered: 1
Top product codes: DRX
Regulation §: 870.2360

Proprietary names: 989803156271 Adult Disp Radiolucent 5 Leadwire Electrode Set, IEC, 989803156231 Adult Disposable Radiolucent 3 Leadwire Electrode Set, IEC, 989803156201 Adult Disposable Metallic 3 Leadwire Electrode Set, AAMI, 989803156241 Adult Disposable Metallic 5 Leadwire Electrode Set, AAMI, 989803156221 Adult Disposable Radiolucent 3 Leadwire Electrode Set, AAMI, 989803156261 Adult Disposable Radiolucent 5 Leadwire Electrode Set, AAMI

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221218950%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1218950