FDA Device Establishments · JSON-LD · Markdown

Philips North America LLC

FEI 1218950 · Repack or Relabel Medical Device · Status: Active

FEI Number1218950
Owner / OperatorPhilips Medical Systems International BV (#1217116)
Address3000 Minuteman Rd, ANDOVER, MA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DRX
Regulation § (21 CFR)870.2360
Proprietary names989803156271 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

External sources

Source: openFDA. Public-domain (CC0).