FDA Device Establishments · JSON-LD · Markdown
FEI 3003337893 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3003337893 |
|---|---|
| Owner / Operator | Nephros, INC. (#9053647) |
| Address | 380 Lackawana Place, South Orange, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KDI |
| Regulation § (21 CFR) | 876.5860 |
| Proprietary names | OLpur MD220 Hemodiafiltration Filter; OLpur H2H Hemodiafiltration Module; H2H Infusion Set; H2H Substitution Filter; H2H Rinse Line; H2H Water Filter; Nephros On-Line Mid-Dilution Hemodiafiltration System |
Source: openFDA. Public-domain (CC0).