FDA Device Establishments · JSON-LD · Markdown
FEI 1222117 · Manufacture Medical Device · Status: Active
| FEI Number | 1222117 |
|---|---|
| Owner / Operator | UNETIXS VASCULAR, INC. (#9000359) |
| Address | 333 Strawberry Field Rd, Suite 11, Warwick, RI, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | JAF |
| Regulation § (21 CFR) | 892.1540 |
| Proprietary names | MultiLab 2000 Series II 2CP-R; MultiLab 2000 Series II Revo w/cart; MultiLab 2000 Series II Roodra; Multilab 2000 Series 2-CP-R,; MultiLab 2000 Series II 2CP-R Express; MultiLab 2000 Series II LHS-TI; Multilab 2000 Series 2 LHS; REVO 1100; Miltilab Series 2 LHS-TI; Multilab Series 2 LHS ERGO |
Source: openFDA. Public-domain (CC0).