FDA Device Establishments · JSON-LD · Markdown
FEI 3018501318 · Manufacture Medical Device · Status: Active
| FEI Number | 3018501318 |
|---|---|
| Owner / Operator | CREWT Medical Systems, INC (#10081331) |
| Address | 3F, TH1 Bldg, 3-11, Tsukudo-machi, Shinjuku-ku Tokyo, 162-0821, JP |
| Mandatory US Agent | Nilo Medical Consulting Group |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HOX |
| Regulation § (21 CFR) | 886.1150 |
| Proprietary names | IMOvifa |
Source: openFDA. Public-domain (CC0).