FDA Device Establishments · JSON-LD · Markdown
FEI 3016701404 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3016701404 |
|---|---|
| Owner / Operator | Philips Medical Systems International BV (#1217116) |
| Address | 1003 Corporate Lane, STE B, Export, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 26 |
| Product codes (top 20) | LKD, NHO, DSK, MHX, CCK, MSX, GWQ, DSF, CBS, DSJ, NHP, KOI, DPS, MLD, GWS, CBQ, CCL, DQA, FLL, BZQ |
| Regulation § (21 CFR) | 868.2480, 868.1500, 870.1110, 870.1025, 868.1400, 870.2300, 882.1400, 870.2810, 868.1620, 870.1100 |
| Proprietary names | IntelliVue Patient Monitor MX450 (866062); IntelliVue Patient Monitor MX400 (866060); IntelliVue Patient Monitor MX550 (866066); IntelliVue Patient Monitor MX500 (866064) |
Source: openFDA. Public-domain (CC0).