FDA Device Establishments · JSON-LD · Markdown
FEI 3042175844 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3042175844 |
|---|---|
| Owner / Operator | Philips Medical Systems International BV (#1217116) |
| Address | VEENPLUIS 6, BEST Noord-Brabant, 5684 PC, NL |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | LLZ, OWB |
| Regulation § (21 CFR) | 892.2050, 892.1650 |
| Proprietary names | Dynamic Coronary Roadmap 2 |
Source: openFDA. Public-domain (CC0).