FDA Device Establishments · JSON-LD · Markdown
FEI 3002807736 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3002807736 |
|---|---|
| Owner / Operator | NIHON SEIMITSU SOKKI CO., LTD. (#8010061) |
| Address | 2508-13 NAKAGO, SHIBUKAWA Gunma, 377-0293, JP |
| Mandatory US Agent | FLORENCE ROSTAMI LAW, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EXR |
| Regulation § (21 CFR) | 876.1800 |
| Proprietary names | Uro Checker |
Source: openFDA. Public-domain (CC0).