FDA Device Establishments · JSON-LD · Markdown
FEI 1000125241 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 1000125241 |
|---|---|
| Owner / Operator | REPROCESSING PRODUCTS CORPORATION (RPC) (#9004570) |
| Address | 1643 W Modern Ct, TUCSON, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FJK |
| Regulation § (21 CFR) | 876.5820 |
| Proprietary names | Recirculation Connectors (Lure Lock) - Sterile - 7001-3902W; SaniGuard Dialysis Catheter Caps - Non-Injectable - Sterile - 7001-3915 |
Source: openFDA. Public-domain (CC0).